Q4 2025 Arvinas Inc Earnings Call

February 24, 2026

Speaker #1: Hello and welcome to the Arvinas Q4 2025 earnings call. All lines have been placed on mute to prevent any background noise. After the speakers' remarks, there will be a question-and-answer session.

Operator: Hello, welcome to the Arvinas Q4 2025 Earnings Call. All lines have been placed on mute to prevent any background noise. After the speaker's remarks, there will be a question and answer session. If you would like to ask a question during this time, simply press Star followed by 1 on your telephone keypad. If you would like to withdraw your question, press Star 1 again. Thank you. I will now turn the call over to Jeff Boyle, Head of Investor Relations. Jeff, you may begin.

Speaker #1: If you would like to ask a question during this time, simply press star followed by the number 1 on your telephone keypad. And if you would like to withdraw your question, press star 1 again.

Speaker #1: Thank you. I will now turn the call over to Jeff Boyle, Head of Impress Relations. Jeff, you may begin.

Speaker #2: Good morning, everyone, and thank you for joining us. Earlier today, we issued a press release with our fourth-quarter and full-year 2025 financial results, which is available in the Investor and Media section of our website at arvinas.com.

Jeff Boyle: Good morning, everyone, and thank you for joining us. Earlier today, we issued a press release with our Q4 and full year 2025 financial results, which is available in the Investor and Media section of our website at arvinas.com. Joining us on the call today, we have Randy Teel, our President and CEO, Noah Berkowitz, our Chief Medical Officer, Angela Cacace, our Chief Scientific Officer, and Andrew Saik, our Chief Financial Officer. Before we begin, I'll remind you that today's discussion contains forward-looking statements that involve risks, uncertainties, and assumptions. These risks and uncertainties are outlined in today's press release and in the company's recent filing with the Securities and Exchange Commission, which I urge you to read. Our actual results may differ materially from what is discussed on today's call.

Speaker #2: Joining us on the call today, we have Randy Teal, our President and CEO; Noah Berkowitz, our Chief Medical Officer; Angela Cacace, our Chief Scientific Officer; and Andrew Saik, our Chief Financial Officer.

Speaker #2: Before we begin, I'll remind you that today's discussion contains forward-looking statements that involve risks, uncertainties, and assumptions. These risks and uncertainties are outlined in today's press release and in the company's recent filing with the Securities and Exchange Commission, which I urge you to read.

Speaker #2: Our actual results may differ materially from what is discussed on today's call. A replay of this call, as well as today's press release and an updated corporate deck, will be available on the Investor and Media section of our website.

Jeff Boyle: A replay of this call, as well as today's press release and an updated corporate deck, will be available on the Investor and Media section of our website. Now I'll turn the call over to Randy Teel. Randy?

Speaker #2: And now I'll turn the call over to Randy Teal. Randy?

Speaker #3: Thanks, Jeff. And thank you all for joining us today. It's an honor and a privilege to lead such a talented and committed team as ARVINAS enters a period where we anticipate multiple value-driving milestones at the company.

Randy Teel: Thanks, Jeff. Thank you all for joining us today. It's an honor and a privilege to lead such a talented and committed team as Arvinas enters a period where we anticipate multiple value-driving milestones at the company. In addition to the team, we have a technology proven in the clinic, an exciting pipeline, and a strong balance sheet, allowing us to continue our work to make a meaningful impact for patients, their families, and our shareholders. 2025 saw meaningful progress across our pipeline and was a transformative year for the company. In addition to submitting our first New Drug Application, setting the stage for potentially the first-ever FDA approval of a PROTAC degrader, we redefined our strategy to maximize the opportunities ahead in each of our core areas of focus.

Speaker #3: In addition to the team, we have a technology proven in the clinic, an exciting pipeline, and a strong balance sheet, allowing us to continue our work to make a meaningful impact for patients, their families, and our shareholders.

Speaker #3: 2025 saw meaningful progress across our pipeline and was a transformative year for the company. In addition to submitting our first new drug application, setting the stage for potentially the first-ever FDA approval of a PROTAC degrader, we redefined our strategy to maximize the opportunities ahead in each of our core areas of focus.

Speaker #3: With four ongoing clinical trials across oncology and neurology, including our recently begun first-in-human trial of our PolyQ AR degrader, ARV027, we believe we have the potential to bring truly differentiated treatments to millions of underserved patients.

Randy Teel: With 4 ongoing clinical trials across oncology and neurology, including our recently begun first-in-human trial of our polyQ-AR degrader, ARV-027, we believe we have the potential to bring truly differentiated treatments to millions of underserved patients. We're entering a pivotal period at Arvinas. As we've been previewing for the past 6 months, 2026 will be defined by multiple data readouts and clinical advancements. We believe these milestones will validate our strategy of developing only treatments that are highly differentiated from other options. I'll summarize clinical data expectations for the year and make a few comments on corporate strategy before turning the call over to the team to walk through recent accomplishments and our forward-looking plans in more detail.

Speaker #3: We're entering a pivotal period at ARVINAS. As we've been previewing for the past six months, 2026 will be defined by multiple data readouts and clinical advancements.

Speaker #3: We believe these milestones will validate our strategy of developing only treatments that are highly differentiated from other options. I'll summarize clinical data expectations for the year and make a few comments on corporate strategy before turning the call over to the team to walk through recent accomplishments and our forward-looking plans in more detail.

Speaker #3: Beginning with our LARC2 degrader, ARV-102, I'm pleased to announce today that data from our Phase 1 clinical trial in patients with Parkinson's disease was accepted for an oral presentation at the Alzheimer's Disease and Parkinson's Disease Conference in March.

Randy Teel: Beginning with our LRRK2 degrader, ARV-102, I'm pleased to announce today that data from our phase 1 clinical trial in patients with Parkinson's disease was accepted for an oral presentation at the Alzheimer's Disease and Parkinson's Disease Conference in March. We'll assess the ability of ARV-102 to degrade LRRK2 in the CSF and see how it impacts important pathway biomarkers. Rather than inhibit LRRK2's kinase activity intermittently, ARV-102 degrades the entire LRRK2 protein, an important consideration when thinking about its potentially differentiated profile. Turning to ARV-806, our KRAS G12D PROTAC potently and selectively eliminates both the on and off forms of the protein.

Speaker #3: We'll assess the ability of ARV-102 to degrade LARC2 in the CSF and see how it impacts important pathway biomarkers. Rather than inhibit LARC2's kinase activity intermittently, ARV-102 degrades the entire LARC2 protein—an important consideration when thinking about its potentially differentiated profile.

Speaker #3: Turning to ARV806, our KRAS G12D PROTAC potently and selectively eliminates both the on- and off forms of the protein. Based on faster-than-expected enrollment in this trial, we now expect to make our first data disclosure for the program by the middle of 2026, and we've already submitted data from that trial for presentation at a medical congress in the coming months.

Randy Teel: Based on faster than expected enrollment in this trial, we now expect to make our first data disclosure for the program by the middle of 2026. We've already submitted data from that trial for presentation at a medical congress in the coming months. This will be an important look at why we believe ARV-806 has the potential to be a clearly differentiated treatment. Stay tuned for more on our disclosure plans. Next, our PROTAC BCL6 degrader, ARV-393, is continuing to progress well in our phase 1 dose escalation trial. We intend to share data from this trial in the second half of 2026. As announced on our last earnings call, we've already seen responses in early cohorts in patients with both B and T cell lymphomas, even at exposures below those predicted to be efficacious.

Speaker #3: This will be an important look at why we believe ARV806 has the potential to be a clearly differentiated treatment, so stay tuned for more on our disclosure plans.

Speaker #3: Next, our PROTAC BCL6 degrader, ARV-393, is continuing to progress well in our Phase 1 dose escalation trial, and we intend to share data from this trial in the second half of 2026.

Speaker #3: As announced on our last earnings call, we've already seen responses in early cohorts in patients with both B and T-cell lymphomas, even at exposures below those predicted to be efficacious.

Speaker #3: We also observed robust BCL6 degradation and the safety profile of 393 supports continued dose escalation. With respect to that dextrin, as you know, we are working with Pfizer to select a third party for its commercialization and potential further development.

Randy Teel: We also observed robust BCL6 degradation. The safety profile of ARV-393 supports continued dose escalation. With respect to Vepdegestrant, as you know, we are working with Pfizer to select a third party for its commercialization and potential further development. Our goal remains to make sure that if it's approved, Vepdeg is launch-ready and available as a potentially best-in-class therapeutic option for patients with ER-positive, HER2-negative, advanced breast cancer in the second-line ESR1 mutant setting. Our discussions to date with potential partners have been productive. We're working to have an agreement in place before the 5 June PDUFA date. Before I turn the call over to the team, I'd like to make two comments on corporate strategy. First, last year, we decided to refocus our resources on our phase 1 clinical programs, which we now have four of.

Speaker #3: Our goal remains to make sure that if it's approved, that deg is launch-ready and available as a potentially best-in-class therapeutic option for patients with ER-positive, HER2-negative, advanced breast cancer in the second line, ESR1 mutant setting.

Speaker #3: Our discussions to date with potential partners have been productive. And we're working to have an agreement in place before the June 5th PDUFA date.

Speaker #3: Finally, before I turn the call over to the team, I'd like to make two comments on corporate strategy. First, last year, we decided to refocus our resources on our Phase I clinical programs which we now have four of.

Speaker #3: While we believe that deg has the potential to be a best-in-class therapy for patients, we think the best way for ARVINAS to create shareholder value is to focus on ARV102, ARV806, ARV393, and now ARV027.

Randy Teel: While we believe Vepdeg has the potential to be a best-in-class therapy for patients, we think the best way for Arvinas to create shareholder value is to focus on ARV-102, ARV-806, ARV-393, and now ARV-027. Second, we recognize the bar is high for all of our programs. We won't settle for as good as. We hope patients don't have to choose between efficacy, safety, and tolerability. We're determined to only develop treatments that are differentiated and will be highly disciplined in moving programs forward. We believe our pipeline is producing potentially transformative treatments for patients, and we look forward to sharing what we believe will be compelling data for each of these programs as we reach milestones in the future. With that, I'll turn the call over to Noah. Noah?

Speaker #3: Second, we recognize the bar is high for all of our programs. We won't settle for as good as, and we hope patients don't have to choose between efficacy, safety, and tolerability.

Speaker #3: We're determined to develop only treatments that are differentiated and will be highly disciplined in moving programs forward. We believe our pipeline is producing potentially transformative treatments for patients, and we look forward to sharing what we believe will be compelling data for each of these programs as we reach milestones in the future.

Speaker #3: With that, I'll turn the call over to Noah. Noah?

Speaker #2: Thanks, Randy. And good morning, everyone. I'll begin with ARV-102, our LARC2 degrader. As background, Angela?

Noah Berkowitz: Thanks, Randy, and good morning, everyone. I'll begin with ARV-102, our LRRK2 degrader. As background, ARV-102, Angela. Angela?

Speaker #4: Thanks, Noah. And good morning, everyone. I'll start by sharing some additional details about ARV027, our PROTAC degrader designed to target the polyglutamine-expanded androgen receptor, or PolyQ AR, in skeletal muscle.

Angela Cacace: Thanks, Noah. Good morning, everyone. I'll start by sharing some additional details about ARV-027, our PROTAC degrader designed to target the polyglutamine expanded androgen receptor, or polyQ-AR, in skeletal muscle. We have deep expertise in developing AR degraders. Our first clinical candidate was an AR degrader, and luxdegalutamide, which we outlicensed to Novartis in 2024, is progressing through multiple phase 2 trials in hormone-sensitive and castrate-resistant prostate cancer. PolyQ-AR is the root cause of disease in spinal-bulbar muscular atrophy, or SBMA, also known as Kennedy's disease. SBMA is a rare genetically driven neuromuscular disease with no approved treatments available and consequently significant unmet need. For background, SBMA is an X-linked disease caused by a CAG expansion in the AR gene, resulting in polyQ-AR accumulation.

Angela M. Cacace: Thanks, Noah. Good morning, everyone. I'll start by sharing some additional details about ARV-027, our PROTAC degrader designed to target the polyglutamine expanded androgen receptor, or polyQ-AR, in skeletal muscle. We have deep expertise in developing AR degraders. Our first clinical candidate was an AR degrader, and luxdegalutamide, which we outlicensed to Novartis in 2024, is progressing through multiple phase 2 trials in hormone-sensitive and castrate-resistant prostate cancer. PolyQ-AR is the root cause of disease in spinal-bulbar muscular atrophy, or SBMA, also known as Kennedy's disease. SBMA is a rare genetically driven neuromuscular disease with no approved treatments available and consequently significant unmet need. For background, SBMA is an X-linked disease caused by a CAG expansion in the AR gene, resulting in polyQ-AR accumulation.

Speaker #4: We have deep expertise in developing AR degraders. Our first clinical candidate was an AR degrader. And LARC2 deglutamide, which we outlicense to Novartis in 2024, is progressing through multiple Phase II trials in hormone-sensitive and castrate-resistant prostate cancer.

Speaker #4: PolyQ AR is the root cause of disease in spinal and bulbar muscular atrophy, or SBMA, also known as Kennedy's disease. SBMA is a rare, genetically driven neuromuscular disease with no approved treatment available and, consequently, significant unmet need.

Speaker #4: For background, SCMA is an X-linked disease caused by a CAG expansion in the AR gene, resulting in PolyQ AR accumulation. This toxic accumulation impairs contractility and causes atrophy and ultimately weakness and loss of endurance in muscle.

Angela Cacace: This toxic accumulation impairs contractility and causes atrophy and ultimately weakness and loss of endurance in muscle. The goal for developing a disease-modifying therapy in SBMA is reducing polyQ-AR in muscle. We believe ARV-027 has the profile to become the first-ever therapy for patients with SBMA that tackles the protein at the genetic root cause of the disease. ARV-027 is a PROTAC that drives degradation of polyQ-AR in skeletal muscle. We presented the first ARV-027 preclinical data last year at the World Muscle Society Congress in October, and we will share data again at the Kennedy's Disease Association conference later this week. These data show with oral ARV-027 induced degradation of muscle polyQ-AR, which resulted in clear functional improvement and extended survival in a rapidly progressing SBMA mouse model.

Angela M. Cacace: This toxic accumulation impairs contractility and causes atrophy and ultimately weakness and loss of endurance in muscle. The goal for developing a disease-modifying therapy in SBMA is reducing polyQ-AR in muscle. We believe ARV-027 has the profile to become the first-ever therapy for patients with SBMA that tackles the protein at the genetic root cause of the disease. ARV-027 is a PROTAC that drives degradation of polyQ-AR in skeletal muscle. We presented the first ARV-027 preclinical data last year at the World Muscle Society Congress in October, and we will share data again at the Kennedy's Disease Association conference later this week. These data show with oral ARV-027 induced degradation of muscle polyQ-AR, which resulted in clear functional improvement and extended survival in a rapidly progressing SBMA mouse model.

Speaker #4: The goal for developing a disease-modifying therapy in SCMA is reducing PolyQ AR in muscle. We believe ARV027 has the profile to become the first-ever therapy for patients with SCMA that tackles the protein at the genetic root cause of the disease.

Speaker #4: ARV027 is a PROTAC that drives degradation of PolyQ AR in skeletal muscle. We presented the first ARV027 preclinical data last year at the World Muscle Society Conference in October, and we will share data again at the Kennedy's Disease Association conference later this week.

Speaker #4: These data show, with oral ARV027-induced degradation of muscle PolyQ AR, which resulted in clear functional improvement and extended survival in a rapidly progressing SCMA mouse model.

Speaker #4: We recently initiated our Phase I trial of ARV027 in healthy volunteers. And are excited to be developing ARV027 for thousands of patients with spinal and bulbar muscular atrophy, a disease with no approved disease-modifying therapies.

Angela Cacace: We recently initiated our Phase 1 trial of ARV-027 in healthy volunteers and are excited to be developing ARV-027 for thousands of patients with spinal-bulbar muscular atrophy, a disease with no approved disease-modifying therapies. Rounding out programs that we expect will enter the clinic this year, we have our first immuno-oncology-focused PROTAC degrader for solid tumors, ARV-6723, that targets HPK1. HPK1 acts as a central intracellular brake on the immune system, suppressing T-cell receptor signaling and broadly dampening both innate and adaptive antitumor responses. Beyond its kinase activity, HPK1 also serves a scaffolding role that reinforces immune suppression, making it an attractive kinase for degradation rather than inhibition. Preclinically, ARV-6723 has shown deep and sustained HPK1 degradation, eliminating both kinase and scaffolding functions, an effect not achieved with kinase inhibition alone.

Angela M. Cacace: We recently initiated our Phase 1 trial of ARV-027 in healthy volunteers and are excited to be developing ARV-027 for thousands of patients with spinal-bulbar muscular atrophy, a disease with no approved disease-modifying therapies. Rounding out programs that we expect will enter the clinic this year, we have our first immuno-oncology-focused PROTAC degrader for solid tumors, ARV-6723, that targets HPK1. HPK1 acts as a central intracellular brake on the immune system, suppressing T-cell receptor signaling and broadly dampening both innate and adaptive antitumor responses. Beyond its kinase activity, HPK1 also serves a scaffolding role that reinforces immune suppression, making it an attractive kinase for degradation rather than inhibition. Preclinically, ARV-6723 has shown deep and sustained HPK1 degradation, eliminating both kinase and scaffolding functions, an effect not achieved with kinase inhibition alone.

Speaker #4: Rounding out programs that we expect will enter the clinic this year, we have our first immuno-oncology-focused PROTAC degrader for solid tumors, ARV-6723, that targets HPK1.

Speaker #4: HPK1 acts as a central intracellular brake on the immune system, suppressing T-cell receptor signaling and broadly dampening both innate and adaptive anti-tumor responses. Beyond its kinase activity, HPK1 also serves a scaffolding role that reinforces immune suppression, making it an attractive kinase for degradation rather than inhibition.

Speaker #4: Preclinically, ARV6723 has shown deep and sustained HPK1 degradation. Eliminating both kinase and scaffolding functions, an effect not achieved with kinase inhibition alone. As a single agent, ARV6723 demonstrated meaningful and durable tumor growth control across multiple syngenetic models, including both high and low immunogenic tumors and outperformed an investigational HPK1 inhibitor and anti-PD1 therapy in several settings.

Angela Cacace: As a single agent, ARV-6723 demonstrated meaningful and durable tumor growth control across multiple syngeneic models, including both high and low immunogenic tumors, and outperformed an investigational HPK1 inhibitor and anti-PD-1 therapy in several settings. It also demonstrated strong activity in combination with anti-PD-1. Mechanistically, HPK1 degradation induces a distinct pro-inflammatory tumor microenvironment with increased activated T cells, NK cells, and monocytes. In addition, ARV-6723 was found to reduce immunosuppressive neutrophils while inducing broader pro-inflammatory pathway activation than inhibition alone. Last week at AACR Immuno-Oncology Conference, we presented preclinical data demonstrating ARV-6723's robust single-agent activity and outperformance when compared to the clinical HPK1 inhibitor in efficacy studies with several mouse models representing hot and cold immunological settings, and demonstrated efficacy in multiple models of anti-PD-1 resistance.

Angela M. Cacace: As a single agent, ARV-6723 demonstrated meaningful and durable tumor growth control across multiple syngeneic models, including both high and low immunogenic tumors, and outperformed an investigational HPK1 inhibitor and anti-PD-1 therapy in several settings. It also demonstrated strong activity in combination with anti-PD-1. Mechanistically, HPK1 degradation induces a distinct pro-inflammatory tumor microenvironment with increased activated T cells, NK cells, and monocytes. In addition, ARV-6723 was found to reduce immunosuppressive neutrophils while inducing broader pro-inflammatory pathway activation than inhibition alone. Last week at AACR Immuno-Oncology Conference, we presented preclinical data demonstrating ARV-6723's robust single-agent activity and outperformance when compared to the clinical HPK1 inhibitor in efficacy studies with several mouse models representing hot and cold immunological settings, and demonstrated efficacy in multiple models of anti-PD-1 resistance.

Speaker #4: It also demonstrated strong activity in combination with anti-PD-1. Mechanistically, HPK1 degradation induces a distinct pro-inflammatory tumor microenvironment, with increased activated T-cells, NK-cells, and monocytes. In addition, ARV-6723 was found to reduce immunosuppressive neutrophils while inducing broader pro-inflammatory pathway activation than inhibition alone.

Speaker #4: Last week, at AACR immuno-oncology conference, we presented preclinical data demonstrating ARV6723's robust single-agent activity and outperformance when compared to the clinical HPK1 inhibitor in efficacy studies with several mouse models representing hot and cold immunological settings and demonstrated efficacy in multiple models of anti-PD1 resistance.

Speaker #4: Collectively, these data position ARV6723 as a potentially differentiated oral immuno-oncology approach designed to drive deeper and more durable anti-tumor responses. ARV6723 has potential to address significant unmet need across multiple settings where currently available immunotherapy drugs have failed.

Angela Cacace: Collectively, these data position ARV-6723 as a potentially differentiated oral immuno-oncology approach designed to drive deeper and more durable antitumor responses. ARV-6723 has potential to address significant unmet need across multiple settings where currently available immunotherapy drugs have failed. Pending regulatory feedback, we are planning to begin first-in-human studies for ARV-6723 later this year, and based on preclinical findings, we believe ARV-6723 could change the treatment paradigm in the immuno-oncology treatment landscape. Finally, we're making strong progress in our oral pan-KRAS PROTAC program, a preclinical program that complements our clinical KRAS G12D degrader. Our pan-KRAS PROTAC differentiates from all inhibitors in that our novel oral degrader is designed to target KRAS for elimination.

Angela M. Cacace: Collectively, these data position ARV-6723 as a potentially differentiated oral immuno-oncology approach designed to drive deeper and more durable antitumor responses. ARV-6723 has potential to address significant unmet need across multiple settings where currently available immunotherapy drugs have failed. Pending regulatory feedback, we are planning to begin first-in-human studies for ARV-6723 later this year, and based on preclinical findings, we believe ARV-6723 could change the treatment paradigm in the immuno-oncology treatment landscape. Finally, we're making strong progress in our oral pan-KRAS PROTAC program, a preclinical program that complements our clinical KRAS G12D degrader. Our pan-KRAS PROTAC differentiates from all inhibitors in that our novel oral degrader is designed to target KRAS for elimination.

Speaker #4: Pending regulatory feedback, we are planning to begin first-in-human studies for ARV6723 later this year and based on preclinical findings, we believe ARV6723 could change the treatment paradigm in the immuno-oncology treatment landscape.

Speaker #4: Finally, we're making strong progress in our oral pan-KRAS PROTAC program, a preclinical program that complements our clinical KRAS G12C degrader. Our pan-KRAS PROTAC differentiates from all inhibitors in that our novel oral degrader is designed to target KRAS for elimination.

Angela Cacace: Preclinically, we've demonstrated broad degradation across KRAS alterations, including wild type amplified KRAS, with selectivity over RAS isoforms and activity in both on and off states. Compared to pan-RAS inhibitors, by degrading and removing the oncoprotein, we've observed stronger antiproliferative and apoptotic effects, greater tumor growth inhibition, and enhanced activity when combined with anti-PD-1 therapy, providing preclinical evidence for a differentiated profile. We will present preclinical data comparing our PROTAC pan-KRAS degrader with pan-RAS inhibitors at the AACR Special Conference on RAS in March, and we will also be presenting data highlighting efficacy in a KRAS engineered model and associated immune microenvironment changes at a scientific congress in the first half of this year. With that, I'll turn the call over to Andrew to review our quarterly financial information. Andrew?

Angela M. Cacace: Preclinically, we've demonstrated broad degradation across KRAS alterations, including wild type amplified KRAS, with selectivity over RAS isoforms and activity in both on and off states. Compared to pan-RAS inhibitors, by degrading and removing the oncoprotein, we've observed stronger antiproliferative and apoptotic effects, greater tumor growth inhibition, and enhanced activity when combined with anti-PD-1 therapy, providing preclinical evidence for a differentiated profile. We will present preclinical data comparing our PROTAC pan-KRAS degrader with pan-RAS inhibitors at the AACR Special Conference on RAS in March, and we will also be presenting data highlighting efficacy in a KRAS engineered model and associated immune microenvironment changes at a scientific congress in the first half of this year. With that, I'll turn the call over to Andrew to review our quarterly financial information. Andrew?

Speaker #4: Preclinically, we've demonstrated broad degradation across KRAS alterations including wild-type amplified KRAS with selectivity over RAS isoforms and activity in both on and off states.

Speaker #4: Compared to pan-RAS inhibitors, by degrading and removing the oncoprotein, we've observed stronger antiproliferative and apoptotic effects, greater tumor growth inhibition, and enhanced activity when combined with anti-PD1 therapy, providing preclinical evidence for a differentiated profile.

Speaker #4: We will present preclinical data comparing our PROTAC pan-KRAS degrader with pan-RAS inhibitors at AACR in March, and we will also be presenting data highlighting efficacy in a KRAS syngeneic model and associated immune microenvironment changes at a scientific congress in the first half of this year.

Speaker #4: With that, I'll turn the call over to Andrew to review our quarterly financial information. Andrew?

Speaker #5: Thanks, Angela. And good morning, everyone. I’m pleased to provide financial highlights for the fourth quarter and full year ended December 31, 2025. As a reminder, detailed financial results for the fourth quarter and year-end, including a reconciliation of GAAP-to-non-GAAP financial measures, are included in the press release we issued this morning.

Andrew Saik: Thanks, Angela. Good morning, everyone. I'm pleased to provide financial highlights for Q4 and full year ended 31 December 2025. As a reminder, detailed financial results for Q4 and year-end, including a reconciliation of GAAP to non-GAAP financial measures, are included in the press release we issued this morning. As we look forward to our anticipated data readouts later this year, we are in a strong financial position to maintain our guidance of cash into the second half of 2028. At the end of Q4, we had just over $685 million in cash equivalents, and marketable securities on the balance sheet, compared with just over $1 billion at the end of 2024.

Speaker #5: As we look forward to our anticipated data readouts later this year, we are in a strong financial position to maintain our guidance of cash into the second half of 2028.

Speaker #5: At the end of the fourth quarter, we had just over $685 million in cash, cash equivalents, and marketable securities on the balance sheet, compared with just over $1 billion at the end of 2024.

Speaker #5: We believe our strong balance sheet will enable us to advance our programs to meaningful data events, which will help us make important portfolio decisions in the coming months and years.

Andrew Saik: We believe our strong balance sheet will enable us to advance our programs to meaningful data events, which will help us make important portfolio decisions in the coming months and years. Turning to the Q4 and full year 2025 financial highlights, during the quarter, we reported $9.5 million in revenue, compared to $59.2 million in revenue for the same period in 2024. The decrease was primarily due to a decrease of $40.3 million of revenue from the Novartis license agreement. We reported $262.6 million in revenue for the year, compared to $263.4 million for fiscal year 2024. General and administrative expenses were $23 million in the Q4, compared to $34.1 million for the same period in 2024.

Speaker #5: Turning to the fourth quarter and full-year 2025 financial highlights, during the quarter we reported $9.5 million in revenue, compared to $59.2 million in revenue for the same period in 2024.

Speaker #5: The decrease was primarily due to a decrease of $40.3 million of revenue from the Novartis license agreement. We reported $262.6 million in revenue for the year, compared to $263.4 million for fiscal year '24.

Speaker #5: General administrative expenses were $23 million in the fourth quarter, compared to $34.1 million for the same period in 2024. The decrease of $11.1 million was primarily due to a decrease in personnel and infrastructure-related costs of $4.4 million and a decrease in costs related to developing our commercial operations of $3.1 million.

Andrew Saik: The decrease of $11.1 million was primarily due to a decrease in personnel and infrastructure-related costs of $4.4 million and a decrease in costs related to developing our commercial operations of $3.1 million. G&A expenses were $95.9 million for the year, compared to $165.4 million in the prior year. Q4 non-GAAP G&A expenses were $15.3 million in 2025, compared to $23.7 million in 2024. Research and development expenses were $61.1 million in the Q4, compared to $83.3 million in the same period of 2024.

Speaker #5: GNA expenses were $95.9 million for the year, compared to $165.4 million in the prior year. Fourth quarter non-gap GNA expenses were $15.3 million in 2025, compared to $23.7 million in 2024.

Speaker #5: Research and development expenses were $61.1 million in the fourth quarter, compared to $83.3 million in the same period of 2024. The decrease of $22.2 million was primarily driven by a decrease in compensation and related personnel expenses of $14.1 million, and a decrease in external expenses of $7.6 million.

Andrew Saik: The decrease of $22.2 million was primarily driven by a decrease in compensation and related personnel expenses of $14.1 million and a decrease in external expenses of $7.6 million. For the year ended 31 December 2025, R&D expenses were $285.2 million, compared to $348.2 million for the prior year. Q4 non-GAAP R&D expenses were $56.5 million in 2025, compared to $70.4 million in 2024. Total non-GAAP expenses for Q4 and full year were $71.8 million and $323.4 million, respectively.

Speaker #5: For the year ended December 31, 2025, R&D expenses were $285.2 million, compared to $348.2 million for the prior year. Fourth quarter non-GAAP R&D expenses were $56.5 million in 2025, compared to $70.4 million in 2024.

Speaker #5: Total non-GAAP expenses for the fourth quarter and full year were $71.8 million and $323.4 million, respectively. Our reduced spend in Q4 is a direct result of our cost-cutting efforts in 2025, and we will continue to look for efficiencies in our operating model this year.

Andrew Saik: Our reduced spend in Q4 is a direct result of our cost-cutting efforts in 2025, and we will continue to look for efficiencies in our operating model this year. As previously announced, in September, our board authorized the repurchase of up to $100 million of our outstanding common stock. As of year-end, we had bought back approximately 10 million shares at an average price per share of $9.09, for a total of $91.9 million, including commissions and excise tax. This program is now suspended, and we have no further plans to repurchase shares. Details of our stock repurchase program can be found in our 10-K, which will be issued later today.

Speaker #5: As previously announced, in September, our board authorized the repurchase of up to $100 million of our outstanding common stock. As of year-end, we had bought back approximately $10 million shares at an average price per share of $9.09 for a total of $91.9 million, including commissions and excise tax.

Speaker #5: This program is now suspended, and we have no further plans to repurchase shares. Details of our stock repurchase program can be found in our 10-K, which will be issued later today.

Speaker #5: As I mentioned, we are maintaining our cash runway guidance into the second half of 2028, which allows us to reach important data readouts and continue prioritizing investments in programs that we believe are truly differentiated and that will provide patients with significant benefit.

Andrew Saik: As I mentioned, we are maintaining our cash runway guidance into the second half of 2028, which allows us to reach important data readouts and continue prioritizing investments in programs that we believe are truly differentiated and that will provide patients with significant benefit. Let me now turn the call back to Randy for closing remarks. Randy?

Speaker #5: Let me now turn the call back to Randy for closing remarks. Randy?

Speaker #6: Thanks, Andrew. I'll summarize and then open the call for questions. Over 2026, we anticipate sharing new clinical data from our Phase 1 trials of ARV-102, ARV-806, and ARV-393.

Angela Cacace: Thanks, Andrew. I'll summarize and then open the call for questions.

Angela M. Cacace: Thanks, Andrew. I'll summarize and then open the call for questions.

Randy Teel: Over 2026, we anticipate sharing new clinical data from our Phase 1 trials of ARV-102, 806, and 393. We expect that our polyQ-AR degrader, which just entered human trials, will be joined in the clinic later this year by our HPK1 degrader. We expect important new trials to begin for both ARV-102 and 393. I believe we're entering a period of meaningful execution and value creation at Arvinas. Very few Phase 1 companies have such a strong pipeline and the capital to reach important milestones. Even fewer have a platform that's already announced positive Phase 3 clinical trial results. This is what makes me so enthusiastic about our upcoming opportunities to make a meaningful impact for patients and shareholders. With that, I'll hand the call to Jeff to start Q&A. Jeff?

Speaker #6: We expect that our PolyQ AR degrader, which just entered human trials, will be joined in the clinic later this year by our HBK1 degrader, and we expect important new trials to begin for both ARV102 and 393.

Speaker #6: I believe we're entering a period of meaningful execution and value creation at ARVINAS. Very few Phase I companies have such a strong pipeline and the capital to reach important milestones, and even fewer have a platform that's already announced positive Phase III clinical trial results.

Speaker #6: This is what makes me so enthusiastic about our upcoming opportunities to make a meaningful impact for patients and shareholders. With that, I'll hand the call to Jeff to start Q&A.

Speaker #6: Jeff?

Speaker #7: Thanks, Randy. And as a reminder, we're always available to take questions offline if you can't join the queue, but for now, I'll ask the operator to open the line for Q&A.

Jeff Boyle: Thanks, Randy. As a reminder, we're always available to take questions offline if you can't join the queue, but for now, I'll ask the operator to open the line for Q&A. Operator?

Speaker #7: Operator?

Speaker #6: Actually, operator, this is Randy jumping back in with a quick change of plans. Before we pass back to the operator and open Q&A, we need to do one more section.

Randy Teel: Actually, operator, this is Randy, jumping back in with a quick change of plans. Before we pass it back to the operator and open Q&A, we need to do one more section. Especially with the storm coming the past couple of days, we prerecorded the prepared remarks to ensure we'd have no technical difficulties. Obviously, we did, and some of you noticed that Noah's section was almost entirely skipped. We will have Noah read his section live now and then jump straight to Q&A after that. Noah.

Speaker #6: Especially with the storm coming the past couple of days, we prerecorded the prepared remarks to ensure we'd have no technical difficulties. Obviously, we did, and some of you noticed that Noah's section was almost entirely skipped.

Speaker #6: So we will have Noah read his section live now, and then jump straight to Q&A after that. Noah?

Speaker #8: Thanks, Randy. Okay. So we'll talk about some of our clinical stage assets here. As background, ARV102 is an oral PROTAC LARC2 degrader intentionally designed to cross the blood-brain barrier and selectively degrade leucine-rich repeat kinase 2 or LARC2.

Noah Berkowitz: Thanks, Randy. Okay, we'll talk about some of our clinical-stage assets here. As background, ARV-102 is an oral PROTAC LRRK2 degrader, intentionally designed to cross the blood-brain barrier and selectively degrade leucine-rich repeat kinase 2 or LRRK2. LRRK2 is a multi-domain protein with three key functions of kinase, GTPase, and scaffolding activities. Together, LRRK2's activities regulate endolysosomal trafficking, and when activity is elevated, the lysosome becomes dysfunctional. This leads to obstructions when clearing the aggregated pathological proteins that would typically be degraded through the properly functioning lysosomal pathway. We believe that degrading LRRK2 has the potential to restore endolysosomal homeostasis and to provide therapeutic benefit in disorders characterized by lysosomal dysfunction. Two of those diseases are progressive supranuclear palsy, or PSP, and Parkinson's disease. Several competitors are pursuing LRRK2 as a target in these diseases.

Speaker #8: LARC2 is a multi-domain protein with three key functions: kinase, GTPase, and scaffolding activities. Together, LARC2’s activities regulate endolysosomal trafficking and, when activity is elevated, the lysosome becomes dysfunctional.

Speaker #8: This leads to obstructions when clearing the aggregated pathological proteins that would typically be degraded through the properly functioning lysosomal pathway. We believe that degrading LARC2 has the potential to restore endolysosomal homeostasis and to provide therapeutic benefit in disorders characterized by lysosomal dysfunction.

Speaker #8: Two of those diseases are progressive supranuclear palsy, or PSP, and Parkinson's disease. Several competitors are pursuing LRRK2 as a target in these diseases. Our PROTAC approach is differentiated because we reduce LRRK2 protein, while competitors only inhibit LRRK2 kinase function.

Noah Berkowitz: Our PROTAC approach is differentiated because we reduce LRRK2 protein, while competitors only inhibit LRRK2 kinase function. By degrading the entire LRRK2 protein complex, we disrupt the key functions believed to be linked to neuroinflammation and lysosomal dysfunction. This is an important consideration when thinking about a differentiated profile, as ARV-102 offers the potential for deeper and more durable therapeutic benefit versus inhibitors. Our confidence in this program is bolstered by the data we've generated from our Phase 1 clinical trials in healthy volunteers in Parkinson's disease. As previously disclosed, ARV-102 has been well tolerated and demonstrated dose-dependent CSF exposure across both trials, indicating excellent brain penetration. We also reported that ARV-102 reduced LRRK2 in the CSF by more than 50% and reduced downstream proteins driven by LRRK2 variants that are elevated in the CSF of patients with Parkinson's disease and linked to lysosomal stress.

Speaker #8: By degrading the entire LARC2 protein complex, we disrupt the key functions believed to be linked to neuroinflammation and lysosomal dysfunction. This is an important consideration when thinking about a differentiated profile as ARV102 offers the potential for deeper and more durable therapeutic benefit versus inhibitors.

Speaker #8: Our confidence in this program is bolstered by the data we've generated from our Phase I clinical trials in healthy volunteers in Parkinson's disease. As previously disclosed, ARV102 has been well-tolerated and demonstrated dose-dependent CSF exposure across both trials indicating excellent brain penetration.

Speaker #8: We also reported that ARV102 reduced LARC2 in the CSF by more than 50% and reduced downstream proteins driven by LARC2 variants that are elevated in the CSF of patients with Parkinson's disease and linked to lysosomal stress.

Noah Berkowitz: Two such proteins, GPNMB and CD68, demonstrate clear and disease-relevant pathway engagement in the central nervous system, even in healthy volunteers, where they would not have been expected to be elevated. Altogether, these data provide further evidence that total protein degradation of LRRK2 kinase may have a best-in-class impact on underlying disease compared to inhibition. As Randy mentioned, we were accepted for oral presentation at ADPD, where we will show pathway biomarker results in patients with Parkinson's disease. We look forward to updating you on these data. Let's turn now to the development plan for ARV-102. As we've previously shared, there is strong evidence that endolysosomal trafficking, driven by increased LRRK2, is associated with a clinically meaningful progression, often within 1 year of PSP, a progressively debilitating neurodegenerative disease that is typically fatal within 5 to 7 years of diagnosis.

Speaker #8: Two such proteins, GP and MB, and CD68, demonstrate clear and disease-relevant pathway engagement in the central nervous system even in healthy volunteers where they would not have been expected to be elevated.

Speaker #8: Altogether, these data provide further evidence that total protein degradation of LAR2C kinase may have a best-in-class impact on underlying disease compared to inhibition. As Randy mentioned, we were accepted for oral presentation at ADPD, where we will show pathway biomarker results in patients with Parkinson's disease.

Speaker #8: We look forward to updating you on these data. Let's turn now to the development plan for ARV-102. As we've previously shared, there is strong evidence that endolysosomal trafficking driven by increased LARC2 is associated with the clinically meaningful progression, often within one year, of PSP—a progressively debilitating neurodegenerative disease that is typically fatal within five to seven years of diagnosis.

Speaker #8: We intend to initiate a Phase IB trial in PSP in the first half of this year with the potential to initiate a registrational trial in late 2026 pending health authority feedback.

Noah Berkowitz: We intend to initiate a Phase 1b trial in PSP in the first half of this year, with the potential to initiate a registrational trial in late 2026, pending health authority feedback. If successful, ARV-102 has the potential to become the first and only disease-modifying treatment for this rare, life-threatening neurological disorder that affects approximately 25,000 people every year in the US. We expect to provide additional updates on our clinical development plans in the coming months. We can now move to our KRAS G12D degrader, ARV-806. I'll say we completed dose escalation for once-weekly administration in our Phase 1 trial, well ahead of plan. We believe that reflects strong clinical investigator interest and high demand for effective KRAS-targeted therapies. ARV-806 targets KRAS G12D for elimination.

Speaker #8: If successful, ARV102 has the potential to become the first and only disease-modifying treatment for this rare, life-threatening neurological disorder that affects approximately 25,000 people every year in the US.

Speaker #8: We expect to provide additional updates on our clinical development plans in the coming months. We can now move to our KRAS G12D degrader, ARV-806.

Speaker #8: And I'll say we completed dose escalation for once-weekly administration in our Phase I trial well ahead of plan. We believe that reflects strong clinical investigator interest and high demand for effective KRAS-targeted therapies.

Speaker #8: ARV806 targets KRAS G12D for elimination. KRAS G12D is a well-known oncogenic driver associated with poor prognoses and resistance to standard treatments across major tumor types including pancreatic colorectal and non-small cell lung cancers.

Noah Berkowitz: KRAS G12D is a well-known oncogenic driver associated with poor prognoses and resistance to standard treatments across major tumor types, including pancreatic, colorectal, and non-small cell lung cancers. Importantly, there are no approved targeted therapies on the market for tumors with KRAS G12D mutations. As a reminder, on our last call, we shared preclinical data presented at the Triple Meeting in October that highlighted the clear differentiation of ARV-806 from both KRAS inhibitors and degraders currently in the clinic. These preclinical data showed ARV-806 to be more than 25-fold more potent in reducing cancer cell proliferation, compared to clinical stage KRAS G12D inhibitors and the leading clinical stage G12D degrader. The data also shows durable degradation greater than 90% for 70 days, sorry, for 7 days after a single dose, with efficacy responses across pancreatic, colorectal, and lung cancer models.

Speaker #8: Importantly, there are no approved targeted therapies on the market for tumors with KRAS G12D mutations. As a reminder, on our last call, we shared preclinical data presented at the triple meeting in October that highlighted the clear differentiation of ARV806 from both KRAS inhibitors and degraders currently in the clinic.

Speaker #8: These preclinical data showed ARV806 to be more than 25-fold more potent in reducing cancer cell proliferation compared to clinical stage KRAS G12D inhibitors and the leading clinical stage G12D degrader.

Speaker #8: The data also showed durable degradation greater than 90% for seven days after a single dose, with efficacy responses across pancreatic, colorectal, and lung cancer models.

Speaker #8: We anticipate sharing initial Phase I clinical data in the coming months. There's a very high bar for differentiation, and we believe ARV806 has the potential to transform the field by exceeding that bar.

Noah Berkowitz: We anticipate sharing initial Phase 1 clinical data in the coming months. There's a very high bar for differentiation, and we believe ARV-806 has the potential to transform the field by exceeding that bar. Let's shift to ARV-393, an oral investigational novel degrader of BCL6, with the potential to become a chemo-free standard of care across non-Hodgkin lymphoma indications. BCL6 has a rapid resynthesis rate and is known to be difficult to target by inhibitors. ARV-393's iterative event-driven mechanism of action counters the rapid resynthesis rate of BCL6, resulting in potent, sustained degradation of the protein. As announced on our Q3 earnings call, we've already observed responses in both B and T cell lymphomas in the early cohorts of our ongoing Phase 1 monotherapy trial, even at exposures below those predicted to be efficacious.

Speaker #8: Let's shift to ARV393 in oral investigational novel degrader of BCL-6 with the potential to become a chemo-free standard of care across non-Hodgkin's lymphoma indications.

Speaker #8: BCL-6 has a rapid resynthesis rate and is known to be difficult to target by inhibitors. ARV-393’s iterative, event-driven mechanism of action counters the rapid resynthesis rate of BCL-6, resulting in potent, sustained degradation of the protein.

Speaker #8: As announced on our Q3 earnings call, we've already observed responses in both B- and T-cell lymphomas in the early cohorts of our ongoing Phase I monotherapy trial.

Speaker #8: Even at exposures below those predicted to be efficacious, we also observed evidence of robust BCL-6 degradation and the safety profile of ARV393 supports continued dose escalation.

Noah Berkowitz: We also observed evidence of robust BCL6 degradation, and the safety profile of ARV-393 supports continued dose escalation. In preclinical data presented last year, ARV-393 showed broad synergistic antitumor activity when combined with standard of care biologics and investigational small molecule inhibitors. In December, we presented compelling preclinical data that support ARV-393 in combination with glofitamab, a CD20-directed bispecific antibody, as a chemotherapy-free combination approach in diffuse large B-cell lymphoma or DLBCL. These data demonstrated tumor growth inhibition of 91% with ARV-393 plus glofitamab dosed sequentially, compared to 36% for glofitamab alone. Additionally, RNA sequencing and biomarker analysis suggested that ARV-393 enhances CD20 expression and genes that promote interferon signaling and antigen presentation, but also downregulated proliferation-associated gene sets.

Speaker #8: In preclinical data presented last year, ARV393 showed broad synergistic anti-tumor activity when combined with standard of care biologics and investigational small-molecule inhibitors. In December, we presented compelling preclinical data that support ARV393 in combination with Glofidimab, a CD20-directed bispecific antibody as a chemotherapy-free combination approach in diffuse large B-cell lymphoma or DLBCL.

Speaker #8: These data demonstrated tumor growth inhibition of 91% with ARV-393 plus glofitamab dosed sequentially, compared to 36% for glofitamab alone. Additionally, RNA sequencing and biomarker analyses suggested that ARV-393 enhances CD20 expression and genes that promote interferon signaling and antigen presentation, but also down-regulates proliferation-associated gene sets.

Speaker #8: Overall, these preclinical data suggest mechanistic synergies between BCL-6 degradation with ARV393 and T-cell engagement. We believe these results bring hope for DLBCL patients left with minimal treatment options when standard-of-care therapies fail.

Noah Berkowitz: Overall, these preclinical data suggest mechanistic synergies between BCL6 degradation with ARV-393 and T cell engagement. We believe these results bring hope for DLBCL patients left with minimal treatment options when standard-of-care therapies fail. With our encouraging preclinical data in hand, we're on track to initiate our phase I combination trial with glofitamab in the first half of this year. Now I'll turn the call over to the operator for Q&A.

Speaker #8: With our encouraging preclinical data in hand, we're on track to initiate our Phase I combination trial with Glofidimab in the first half of this year.

Speaker #8: So now I'll turn the call over to the operator for Q&A.

Speaker #1: Thank you, Noah. We will now begin the question-and-answer session. If you would like to ask a question at this time, simply press star followed by the number 1 on your telephone keypad.

Operator: Thank you, Noah. We will now begin the question-and-answer session. If you would like to ask a question at this time, simply press star followed by the number one on your telephone keypad. We will pause for a brief moment to compile the Q&A roster. Our first question comes from the line of Jonathan Miller with Evercore ISI. Jonathan, please go ahead.

Speaker #1: We will pause for a brief moment to compile the Q&A roster. And our first question comes from the line of Jonathan Miller with Evercore ISI.

Speaker #1: Jonathan, please go ahead.

Jonathan Miller: Hey, guys. Thanks so much for taking my question, and congrats on all the progress across the multiple interesting-looking programs. One thing that I immediately react to in some of your prepared remarks is your assertion that you're only going to develop programs for which you're going to see differentiated activity. You know, multiple of these programs are in competitive areas, as you're well aware. I want to ask, across the pipeline, at what point are you gonna get the killer data that determines to you whether or not a program is differentiated? Obviously, that's different for different programs, but could you just go through the pipeline and tell us what you think the key experiment is that'll let you know if you've got something truly differentiated or not?

Speaker #2: Hey, guys. Thanks so much for taking my question, and congrats on all the progress across multiple interesting-looking programs. One thing that I immediately react to in some of your prepared remarks is your assertion that you're only going to develop programs for which you're going to see differentiated activity. Multiple of these programs are in competitive areas, as you're well aware.

Speaker #2: So I wanted to ask across the pipeline, at what point are you going to get the killer data that determines to you whether or not a program is differentiated?

Speaker #2: And obviously, that's different for different programs, but could you just go through the pipeline and tell us what you think the key experiment is that'll let you know if you've got something truly differentiated or not?

Speaker #3: Yeah, John, thanks very much for the question. And just as we started the Q&A, I apologize again to all the folks on the call for the confusion there.

Noah Berkowitz: Yeah, John, thanks very much for the question. Just as we start the Q&A, I apologize again to all the folks on the call for the confusion there. I hope that was clear as we had to re-redo Noah's section. John, that's probably a question we could spend a lot of the day on, right? To your point, for each program, it's going to be different. Certainly, as we think about a plan where we need to be clearly differentiated against competitors, which I think is actually pretty reasonable, does not necessarily mean that when you first show data in a very early Phase 1 trial, that it has to be, you know, beating a competitor that has expansion data, Phase 3 data, and so on.

Speaker #3: I hope that was clear, as we had to redo Noah's section. John, that's probably a question we could spend a lot of the day on.

Speaker #3: Right? So to your point, for each program, it's going to be different. And certainly, as we think about a plan where we need to be clearly differentiated against competitors, which I think is actually pretty reasonable, does not necessarily mean that when you first show data in a very early Phase I trial that it has to be beating a competitor that has expansion data Phase III data and so on.

Speaker #3: So I'll pass to Noah here in a little bit to talk, maybe program by program, for some details that we expect to have this year—probably the right place to focus.

Noah Berkowitz: I'll pass to Noah here in a little bit to talk, you know, maybe program by program for some details that we expect to have this year, probably the right place to focus. As we look across, you know, maybe I'll highlight a couple of things. For LRRK2, for ARV-102 or LRRK2 degrader, the competition there is inhibitors. It'll be really important to show that degradation leads to a different result than inhibition for a target that has not been proven to modify disease overall by drugs that the industry has produced. That's the key risk. For ARV-806, for KRAS G12D, the target's much more validated, but the competitive space is much more intense in terms of other programs that have been out there ahead of it.

Speaker #3: But as we look across maybe I'll highlight a couple of things. For LARC2, for ARV102 or LARC2 degrader, the competition there is inhibitors. It'll be really important to show that degradation leads to a different result in inhibition.

Speaker #3: For a target that has not been proven to modify disease overall by drugs that the industry has produced. So that's the key risk. For 806, for KRAS G12D, the target's much more validated, but the competitive space is much more intense in terms of other programs that have been out there ahead of it.

Speaker #3: For BCL-6, similarly, it's a relatively new target, but there are competitors out there that have paved the way a little bit showing that the target has now become somewhat validated.

Noah Berkowitz: For BCL6, similarly, it's a relatively new target, but there are competitors out there, that have paved the way a little bit, showing that the target has now become somewhat validated. Maybe we'll leave ARV-027 to the side for the moment.

Speaker #3: And maybe we'll leave 027 to the side for the moment. But I think for each of those, the Phase I data will be of some interest, and as we move forward, we'll have to compare over time.

Randy Teel: ... I think for each of those, the phase 1 data will be of some interest, and as we move forward, we'll have to compare over time. Noah, anything else you want to add, you know, maybe specifically around some of the nearer-term data updates?

Speaker #3: Noah, anything else you want to add, maybe specifically around some of the near-term data updates?

Speaker #2: Sure. Thanks, Randy. Yeah, let's take the example of ARV-102 for starters. So, in that case, we have signaled pretty significant conviction. We've said we're starting a trial in PSP this year.

Noah Berkowitz: Sure. Thanks, Randy. Yeah, let's take the example of ARV-102 for starters. In that case, we have, we've signaled pretty significant conviction. We've said we're starting a trial in PSP this year, and regulatory permitting, we may even be able to move towards a registration quality trial, you know, before the end of the year. We believe that we've established our superiority already. We recognize that there are properties of a LRRK2 inhibitor that can be exceeded with LRRK2 degraders. We've shown already in healthy volunteers that we can achieve more than 50% LRRK2 degradation in the brain. That's been our target.

Speaker #2: And regulatory permitting, we may even be able to move towards a registration quality trial. Before the end of the year. So we believe that we've established our superiority already.

Speaker #2: We recognize that there's a property for there are properties of a LARC2 inhibitor that can be exceeded with LARC2 degraders. We've shown already in healthy volunteers that we have more than 50 we can achieve more than 50% LARC2 degradation in the brain that's been our target.

Speaker #2: We've been communicating that clearly because we know in general, like if you want to just simplify in broader strokes, that patients with Parkinson's disease have twice to three times the level of LARC2 protein expression in the brain compared to their age-matched controls.

Noah Berkowitz: We've been communicating that clearly, because we know in general, like, if you want to just simplify, you know, in broader strokes, that patients with Parkinson's disease have twice to three times the level of LRRK2 protein expression in the brain compared to their age-matched controls. Our goal was to achieve that, something that can't be touched by inhibitors. That's why we have lots of conviction there, plus pathway data. More to come at ADPD in April. Now, if I shift for a moment to 806. 806 is a very competitive space. We know that there are many other G12D-targeting drugs ahead of us, mostly inhibitors and let's say one degrader. Fundamentally, that, it really makes it easier for us because we know where the bar is.

Speaker #2: So our goal was to achieve that—something that can't be touched by inhibitors. So that's why we have lots of conviction there, plus pathway data; more to come at ADPD in April.

Speaker #2: Now, if I shift for a moment to 806, 806 is a very competitive space. We know that there are many other G12D targeting drugs ahead of us.

Speaker #2: Mostly inhibitors and, let's say, one degrader. But fundamentally, it really makes it easier for us because we know where the bar is. We know that and I'm going to speak in broad terms.

Noah Berkowitz: We know that. I'm gonna speak in broad terms. I'm not setting the bogey here because this is not so, because it's an imprecise science. We know that we have to be better than, let's say, 35% response rates in this space to be differentiated. We're gonna have to generate data that gives us confidence that we're better. We'll signal as the year moves on, about exactly what level of confidence we have and what, you know, as we can share data with folks. That's clear from the numerous drugs that are in the clinic today, that we have to be better than, you know, the large majority of them, which, you know, would put us in that range. When it comes to ARV-393, we're kind of at the front right now.

Speaker #2: I'm not setting the bogey here, because this is not so—because it's an imprecise science. But we know that we have to be better than, let's say, 35% response rates in this space to be differentiated.

Speaker #2: So we're going to have to generate data that gives us confidence that we're better. We'll signal, as the year moves on, about exactly what level of confidence we have.

Speaker #2: And as we can share data with folks. But that's clear from the numerous drugs that are in the clinic today. That we have to be better than the large majority of them, which would put us in that range.

Speaker #2: And then, when it comes to 393, we're kind of at the front right now. There is a competitor that has shared data, and we do see that there's activity with their drug.

Noah Berkowitz: There is a competitor that has shared data. We do see that there's activity with their drug. This is really early days. Like, we are months or maybe, you know, I don't want to give a specific timeframe that we're behind. It's hard to know, but we're basically at the leading edge of this right now. We're gonna look at the data that's shared by our competitor. We'll look at the data that we generate. We'll share that. We believe that for all three of these drugs, there will be data this year to demonstrate their differentiation that we should, you know, over the course of the year, been able to share with our investors.

Speaker #2: But this is really early days. We are months or maybe I don't want to give a specific time frame that we're behind. It's hard to know.

Speaker #2: But we're basically at the leading edge of this right now. So we're going to look at the data that's shared by our competitor. We'll look at the data that we generate.

Speaker #2: We'll share that. And we believe that for all three of these drugs, there will be data this year to demonstrate their differentiation. That we should, over the course of the year, have been able to share with our investors.

Speaker #3: And thanks so much.

Ted Tenthoff: Thanks so much.

Speaker #1: And your next question comes from the line of Ted Tandoff with Piper Sandler. Ted, please go ahead.

Operator: Your next question comes from the line of Ted Tenthoff with Piper Sandler. Ted, please go ahead.

Ted Tenthoff: Great. Thank you very much. Randy, congratulations and the whole team, I really appreciate the energy you guys are bringing. It's really exciting to have this early-stage program advancing in so many really unique shots on goal here. I wanted to pick back up with what Noah was saying about 102. What really should we be expecting from that data at ADPD? Would there be an incremental PSP update ahead of the registrational trial initiation? I love the speed with which you're moving here, but I wanna understand sort of what the bar is to moving into registrational studies. Thank you.

Speaker #4: Great. Thank you very much. Randy, congratulations. And the whole team, I really appreciate the energy you guys are bringing is really exciting to have this early-stage program advancing in so many really unique shots on goal here.

Speaker #4: I wanted to pick back up with what Noah was saying about 102. What really should we be expecting from that data at ADPD? And would there be an incremental PSP update ahead of the registrational trial initiation?

Speaker #4: I love the speed with which you're moving here. But I want to understand, sort of, what the bar is to moving into registrational studies.

Speaker #4: Thank you.

Speaker #3: Maybe I'll take the second part of that and then pass back for the expectations for ADPD. Ted, I think the answer to that is no.

Randy Teel: Maybe I'll take the second part of that and then pass back for the expectations for ADPD. Ted, I think the answer to that is no. Just the reason is the timing that we laid out in the prepared remarks just now, is that we are anticipating starting a Phase 1b in PSP sooner. Then, as we've said, look, all things going our way and pending some further data from ADPD and regulatory go ahead, we would hope to start a registrational trial by the end of the year. I think the data there in between of starting the PSP trial earlier in the year and then getting to a second one later, I think would prevent that.

Speaker #3: And just the reason is, the timing that we laid out in the prepared remarks just now is that we are anticipating starting a Phase 1B and PSP sooner.

Speaker #3: And then as we've said, look, all things going our way and pending the further data from ADPD and regulatory go ahead, we would hope to start a registrational trial by the end of the year.

Speaker #3: So, I think the data there, in between starting the PSP trial earlier in the year and then getting to a second one later, I think would prevent that.

Speaker #3: But we think that the data that we will be showing at ADPD, which are in Parkinson's patients, will be relevant for both moving forward in PD or PSP.

Randy Teel: We think that the data that we will be showing at ADPD, which are in Parkinson's patients, will be relevant for both moving forward in PD or PSP. Noah, back to you for the ADPD view.

Speaker #3: But Noah, back to you for the ADPD view.

Noah Berkowitz: Sure. Look, we can't pre-release results, but I can, we can, I guess I can frame it. We shared data months ago about, or, you know, that started last year and culminated in biomarker data some months ago in the healthy volunteer population. Now we will share data in the Parkinson's disease patient population. Questions that I think a discerning scientist would be looking for it, are: Well, what happens in Parkinson's disease? Is the drug demonstrating continued safety like was observed in healthy volunteers, because now patients are older? 25 years median age for healthy volunteers, much older for Parkinson's disease patients. There's much more elevated LRRK2 in the CSF at baseline.

Speaker #2: Sure. So look, we can't pre-release results, but I can we can I guess I can frame it. We share data months ago about or that started last year and culminated in biomarker data some months ago.

Speaker #2: In the healthy volunteer population. So now we will share data in the Parkinson's disease patient population. Questions that I think a discerning scientist would be looking for are well, what happens in Parkinson's disease is the drug demonstrating continued safety, like was observed in healthy volunteers because now patients are older.

Speaker #2: 25 years median age for healthy volunteers, much older for Parkinson's disease patients. There's much more elevated LARC2 in the CSF at baseline. So with something that was observed at low levels, now repeated at higher levels because you have to overcome even more LARC2 presence in the brain and obviously these deep portions in the brain, which is represented by the CSF levels.

Noah Berkowitz: It was something that was observed at low levels, now repeated at higher levels, 'cause you have to overcome even more LRRK2 presence in the brain, and obviously these deep portions in the brain, which is, you know, represented by the CSF levels. The biomarker story, right? The biomarkers that were seen in healthy volunteers, is that a, you know, like a once, a finding that can't be replicated, or is it something where the pattern continues or it intensifies when you look at Parkinson's disease patients? That would be the kind of set of questions that I'd look at, and we hope that we can answer those questions at the meeting.

Speaker #2: And then the biomarker story, right? The biomarkers that were seen in healthy volunteers is that a like a once a finding that can't be replicated?

Speaker #2: Or is it something where the pattern continues or it intensifies when you look at Parkinson's disease patients? That would be the kind of set of questions that I'd look at.

Speaker #2: And we hope that we can answer those questions at the meeting.

Ted Tenthoff: That's great. Really helpful, and looking forward to all the other data and updates and progress as well. Thanks.

Speaker #4: That's great. Really helpful. And looking forward to all the other data and updates and progress this year. Thanks.

Speaker #1: And our next question comes from the line of Tyler Van Buren with TD Cowen. Tyler, please go ahead.

Operator: Our next question comes from the line of Tyler Van Buren with TD Cowen. Tyler, please go ahead.

Speaker #5: Hi, this is Frances on for Tyler. Just one quick question on our end. Can you elaborate more on the PAN KRAS presentation at AACR and what we should expect to see from it, as well as what competitors you're using?

[Analyst] (TD Cowen): Hi, this is Francis on for Tyler. Just one quick question on our end. Can you elaborate more on the pan-KRAS presentation at AACR and what we should expect to see from it, as well as what competitors you're using?

Tyler Van Buren: Hi, this is Francis on for Tyler. Just one quick question on our end. Can you elaborate more on the pan-KRAS presentation at AACR and what we should expect to see from it, as well as what competitors you're using?

Speaker #2: Sure. I'll maybe I'll pass to Angela in a moment to talk a bit about that. And as you point out, we have a PAN KRAS program that, as we talked about, is moving ahead preclinically behind the KRAS G12D degrader that will have data at some point this year.

Randy Teel: Sure. Maybe I'll pass to Angela in a moment to talk a bit about that. As you point out, we have a pan-KRAS program that, as we talked about, is moving ahead preclinically, behind the KRAS G12D degrader that will have data at some point this year. Angela, a bit more on the AACR data for pan-RAS.

Speaker #2: But Angela, a bit more on the AACR data for PAN RAS?

Speaker #6: Sure. Thank you for the question. We will be sharing data comparing to the inhibitor. So our goal in the PAN KRAS story is, of course, to remove the ONCO protein.

Angela Cacace: Sure. Thank you for the question. We will be sharing data comparing to the inhibitor. You know, our goal in the pan-KRAS story is, of course, to remove the oncoprotein. We differentiate from the on and the off inhibitors, and that we are removing the inhibitor. First and foremost, what's observed when, as a regulatory mechanism, when you treat with an inhibitor, is compensatory upregulation of KRAS. This is something that's seen with the on inhibitors. You know, we will share KRAS amplified data, so we will be sharing how we compare to the KRAS on inhibitor in that setting. We'll also share some of the mutant data as well, in terms of the activity that we see, the antitumor activity.

Angela M. Cacace: Sure. Thank you for the question. We will be sharing data comparing to the inhibitor. You know, our goal in the pan-KRAS story is, of course, to remove the oncoprotein. We differentiate from the on and the off inhibitors, and that we are removing the inhibitor. First and foremost, what's observed when, as a regulatory mechanism, when you treat with an inhibitor, is compensatory upregulation of KRAS. This is something that's seen with the on inhibitors. You know, we will share KRAS amplified data, so we will be sharing how we compare to the KRAS on inhibitor in that setting. We'll also share some of the mutant data as well, in terms of the activity that we see, the antitumor activity.

Speaker #6: So, we differentiate from the ON and the OFF inhibitors in that we are removing the inhibitor, first and foremost. What's observed as a regulatory mechanism when you treat with an inhibitor is compensatory upregulation of KRAS.

Speaker #6: So this is something that's seen with the ON inhibitors. And so we will share KRAS amplified data. So we will be sharing how we compare to the KRAS ON inhibitor in that setting.

Speaker #6: And then we'll also share some of the median data as well in terms of the activity that we see. The anti-tumor activity. So expect to see those data as well.

Angela Cacace: Expect to see those data as well. I hope that helps.

Angela M. Cacace: Expect to see those data as well. I hope that helps.

Speaker #6: I hope that helps. And then we'll also share some syngenetic model data in the presence of an intact immune system. So I think that's also important with respect to the PAN RAS inhibitors.

[Analyst] (TD Cowen): Thanks so much.

Tyler Van Buren: Thanks so much.

Angela Cacace: We'll also share some syngeneic model data in the presence of an intact immune system. I think that's also important with respect to the pan-RAS inhibitors with respect to our pan-KRAS molecule, that's selective for KRAS versus pan-RAS. We're not hitting N-ras and H-ras. That affects T-cell activity. Yep.

Angela M. Cacace: We'll also share some syngeneic model data in the presence of an intact immune system. I think that's also important with respect to the pan-RAS inhibitors with respect to our pan-KRAS molecule, that's selective for KRAS versus pan-RAS. We're not hitting N-ras and H-ras. That affects T-cell activity. Yep.

Speaker #6: With respect to our PAN KRAS molecule that's selective for KRAS versus PAN RAS. So we're not hitting NHRAS. That affects T-cell activity. Yeah.

Speaker #1: And our next question comes from the line of Akash Tawari with Jeffery's Akash. Please go ahead.

Operator: Our next question comes from the line of Akash Tewari with Jefferies. Akash, please go ahead.

Noah Berkowitz: Hey, this is Manoj on for Akash. Thanks for taking our questions. Just one on ARV-393. What are your early observations around the plasma exposure dynamics when ARV-393 is used in combo with glofitamab? Do you expect the need of any specific dose modifications on either 393 or glofitamab when used in combo in clinics? Also, just one more. Do you see any increased interest for Vepdegestrant after the recent Roche Vepdegestrant data, especially in the earlier settings? Thanks.

Manoj Garg: Hey, this is Manoj on for Akash. Thanks for taking our questions. Just one on ARV-393. What are your early observations around the plasma exposure dynamics when ARV-393 is used in combo with glofitamab? Do you expect the need of any specific dose modifications on either 393 or glofitamab when used in combo in clinics? Also, just one more. Do you see any increased interest for Vepdegestrant after the recent Roche Vepdegestrant data, especially in the earlier settings? Thanks.

Speaker #7: Hey, this is Manoj on for Agas. Thanks for taking our question. Just for a known ARV393, what are your yearly observations around the plasma exposure dynamics when ARV393 is used in combo with glopidimum?

Speaker #7: Do you expect the need of any specific dose modifications on either 393 or glopidimab when used in combo in clinics? And also, just one more.

Speaker #7: Do you see any increased interest for web digestion after the recent Roche digestion data? Especially in the earlier settings. Thanks.

Speaker #3: You know, maybe I'll try to rephrase. I think the first question around 393 was, in broad strokes, do we expect the need to do any dose modification for 393 with glopi?

Randy Teel: You know, maybe I'll try to rephrase. I think the first question around ARV-393 was do we in broad strokes was, do we expect the need to do any dose modification for ARV-393 with glofitamab? Maybe I'll let Noah comment on that in a moment, as we have had some data there late last year. Maybe I can take the second one. Look, we think that the Roche data from late last year validates the hypothesis that an ER therapy will work where ER is driving disease, which is what we've always believed. Really, no, I don't see a concern there.

Speaker #3: And maybe I'll let Noah comment on that in a moment. As we have had some data there late last year. And maybe I can take the second one.

Speaker #3: Look, we think that the Roche data from late last year validate the hypothesis that a therapy will work where it is driving disease. Which is what we've always believed.

Speaker #3: And so really, no. I don't see a concern there. It's certainly validates what we thought would be the case. And we hope that as we're out with our partners at Pfizer looking for a new partner to commercialize, and preferably continue to develop that, it gives somebody the enthusiasm to do that.

Randy Teel: It certainly validates what we thought would be the case, and we hope that as we're out with our partners at Pfizer, looking for a new partner to commercialize and preferably continue to develop that, it gives somebody the enthusiasm to do that. No, I don't see that as an issue. Noah, back to you on the 393 and the potential for requiring dose modifications based on the data we've shown to date.

Speaker #3: So, no, I don't see that as an issue. But Noah, back to you on 393 and the potential for requiring dose modifications based on the data we've shown to date.

Speaker #2: We don't really anticipate that we'll require dose modifications, although obviously in an abundance of caution, we will have some dose escalation. To evaluate the combination.

Noah Berkowitz: We don't really anticipate that we'll require dose modifications, although obviously, you know, in an abundance of caution, we will have some dose escalation to evaluate the combination. There's non-overlapping tox, which is to say that the principal tox for glofitamab is gonna be things like CRS, and also there may be some accumulated hematopoietic toxicity for patients from glofi. We, on the other hand, are not really seeing toxicity in those categories at all. You know, we will be advancing it cautiously, but don't anticipate those modifications.

Speaker #2: There's non-overlapping talks, which is to say that the principal talks for glopidimab is going to be things like CRS and also there may be some accumulated hematopoietic toxicity for patients from glopi.

Speaker #2: But we on the other hand are not really seeing toxicity in those categories at all. So we will be advancing it cautiously, but don't anticipate dose modifications.

Speaker #7: Yeah. Thank you.

[Analyst] (TD Cowen): Yes. Thank you.

Tyler Van Buren: Yes. Thank you.

Noah Berkowitz: Yep.

Speaker #1: And your next question comes from the line of Yigal Nakamovitz with Citi. Yigal, please go ahead.

Operator: Your next question comes from the line of Yigal Nochomovitz with Citi. Yigal, please go ahead.

[Analyst] (Citigroup): Hi, this is Caroline on for Yigal. Thanks for taking our question. Digging in more on LRRK2 and the biomarker data to be presented at ADPD, can you tell us how this data will support the therapeutic hypothesis in PSP? Relatedly, what percent of PSP patients have elevated LRRK2, and are the same biomarker pathways relevant as in Parkinson's? Thanks.

Caroline Palomeque: Hi, this is Caroline on for Yigal. Thanks for taking our question. Digging in more on LRRK2 and the biomarker data to be presented at ADPD, can you tell us how this data will support the therapeutic hypothesis in PSP? Relatedly, what percent of PSP patients have elevated LRRK2, and are the same biomarker pathways relevant as in Parkinson's? Thanks.

Speaker #6: Hi, this is Caroline on for Yigal. Thanks for taking our question. So digging in more on LARC2 and the biomarker data to be presented at ADPD, can you tell us how this data will support the therapeutic hypothesis in PSP?

Speaker #6: And relatedly, what percent of PSP patients have elevated LARC2? And are the same biomarker pathways relevant as in Parkinson's? Thanks.

Speaker #3: Yeah, I'm going to pass that one pretty quickly over to Angela. We've had a few comments on the biomarkers, but Angela, please dig in.

Randy Teel: Yeah, I'm going to pass that one pretty quickly over to Angela. We've had a few comments on the biomarkers, but Angela, please dig in.

Speaker #6: Sure. So in PSP, there's been some recent publications showing that PSP you see the same pathways increase. So you see elevated endolysosomal pathway engagement, uniformly in progressive supernuclear palsy.

Angela Cacace: Sure. In PSP, there's been some recent publications showing that PSP, you see the same pathways increase. You see elevated endolysosomal pathway engagement uniformly in progressive supranuclear palsy and LRRK2 elevation in that population. You know, we expect within that population that we'll see efficacy there. Within that population, when you subset that population and look specifically at LRRK2 elevation, you do see accelerated progression and clinically meaningful progression with, you know, if you do look specifically at the elevated population, you do see acceleration by a year. It's, you know, it clinically meaningful, you know, upwards around 20 to 30 points of the rating scale. Ed Jabbari and his colleagues at the University College London have shown that.

Angela M. Cacace: Sure. In PSP, there's been some recent publications showing that PSP, you see the same pathways increase. You see elevated endolysosomal pathway engagement uniformly in progressive supranuclear palsy and LRRK2 elevation in that population. You know, we expect within that population that we'll see efficacy there. Within that population, when you subset that population and look specifically at LRRK2 elevation, you do see accelerated progression and clinically meaningful progression with, you know, if you do look specifically at the elevated population, you do see acceleration by a year. It's, you know, it clinically meaningful, you know, upwards around 20 to 30 points of the rating scale. Ed Jabbari and his colleagues at the University College London have shown that.

Speaker #6: And LARC2 elevation in that population. And so we expect within that population that we'll see efficacy there. So within that population, when you subset that population, and look, specifically at LARC2 elevation, you do see accelerated progression and clinically meaningful progression.

Speaker #6: If you do look specifically at the elevated population, you do see acceleration by a year and it's clinically meaningful upwards around 20 to 30 points of the rating scale.

Speaker #6: So Ed Jabari and his colleagues at University College London have shown that. So, those data point to, within that genetically defined population, that that's the case.

Angela Cacace: You know, those data point to within that, genetically defined population, that that's the case. You know, we're in. Anytime you see an increase in elevated expression, you know for a PROTAC, that's the place you want to go. PSP is a place where we can prove a concept within a year. We're encouraged by that and, you know, remain very committed to this therapeutic hypothesis in PSP.

Angela M. Cacace: You know, those data point to within that, genetically defined population, that that's the case. You know, we're in. Anytime you see an increase in elevated expression, you know for a PROTAC, that's the place you want to go. PSP is a place where we can prove a concept within a year. We're encouraged by that and, you know, remain very committed to this therapeutic hypothesis in PSP.

Speaker #6: So we're anytime you see an increase in elevated expression, you know for a PROTAC, that's the place you want to go. So PSP is a place where we can prove a concept within a year.

Speaker #6: So we're encouraged by that. And remain very committed to this therapeutic hypothesis. In PSP.

Speaker #5: Got it. Thank you. And separately, is there any update on selecting a third party for VEPTEG? Thanks.

[Analyst] (Citigroup): Got it. Thank you. Separately, is there any update on selecting a third party for PROTAC? Thanks.

Caroline Palomeque: Got it. Thank you. Separately, is there any update on selecting a third party for PROTAC? Thanks.

Randy Teel: Not further than what we put in the remarks this morning. That's on track. We feel good about that process that we're pursuing alongside Pfizer. All is on track, and we hope to have a partner in place by the PDUFA date in early June.

Speaker #3: Not further than what we put in the remarks this morning. That's on track. We feel good about that process that we're pursuing alongside Pfizer, but all is on track and we hope to have a partner in place by the PDUFA date in early June.

Speaker #5: Understood. Thanks.

[Analyst] (Citigroup): Understood. Thanks.

Caroline Palomeque: Understood. Thanks.

Speaker #1: And your next question comes from the line of Derek Archulia with Wells Fargo. Derek, please go ahead.

Operator: Your next question comes from the line of Derek Archila with Wells Fargo. Derek, please go ahead.

Speaker #2: Good morning. This is Jacob On for Derek. Thanks for taking our question. Just one on LARC2 from us. How should we be thinking about safety in the upcoming ADPD readout?

[Analyst] (Wells Fargo): Good morning. This is Jacob on for Derek. Thanks for taking our question. Just one on LRRK2 from us. How should we be thinking about safety in the upcoming ADPD readout? I know it's a relatively short study, but given the lung biology associated with LRRK2, do you think there is anything that would emerge or be looking for at this time point to give you more confidence in a longer duration study?

Speaker #2: I know it's a relatively short study, but given the lung biology associated with LARC2, do you think there's anything that would emerge or be looking for at this time point to give you more confidence in a longer duration study?

Speaker #3: Yeah, that will certainly be an important part of the readout, although as you've talked about, it's still a relatively short duration. Noah, any other comments to make on safety?

Randy Teel: That will certainly be an important part of the readout, although as you've talked about, it's still a relatively short duration. Noah, any other comments to make on safety?

Speaker #4: Sure. So, overall, the Parkinson's disease patients study that we'll be sharing have had 28 days of treatment for patients. We should keep it. So we're doing standard observations of patients.

Noah Berkowitz: Sure. Overall, where the Parkinson's disease patients study that we'll be sharing have had 28 days of treatment for patients. We should keep it... you know, we're doing standard observations of patients to assure safety and assure that there are no findings. I'm not going to provide the data here on the call, that's something to look at at the meeting. I think it's important to recognize that there is an on-target activity that you've identified in the lung of patients that requires tracking, that's why anyone in this space will do things like LFTs, I'm sorry, PFTs, pulmonary function tests, they could be following that up with high-resolution CT scans of the lung if there's anything suspicious.

Speaker #4: To assure safety and assure that there are no findings, I'm not going to provide the data here on the call, but that's something to look at at the meeting.

Speaker #4: I think it's important to recognize that there is an on-target activity that you've identified in the lung of patients that requires tracking. And that's why anyone in this space will do things like LFTs.

Speaker #4: I'm sorry, PFTs, pulmonary function tests, and that could be following that up with high-resolution CT scans of the lung if there's anything suspicious. And the goal will be to demonstrate in the end that you have the right benefit-risk for a drug.

Noah Berkowitz: The goal will be to demonstrate in the end that you have the right benefit risk for a drug. We anticipate that that should be fine. The, you know, I'll point out that it's so standard that there's something called the LIGHT Initiative, which is a recommendation from experts about anyone who's dealing with LRRK2 targeting agents should be thinking about pulmonary function monitoring. It's something we've incorporated into our study, and we'll provide updates at an appropriate meeting.

Speaker #4: And we anticipate that that should be fine. The I'll point out that it's so standard that there's something called a light initiative, which is a recommendation from experts about anyone who's dealing with LARC2 targeting agents should be thinking about pulmonary function monitoring.

Speaker #4: So it's something we've incorporated into our study and we'll provide updates at an appropriate meeting.

Speaker #1: Got it. Thank you. And on a related point, does dose selection read through directly from Parkinson's to PSP, you think?

[Analyst] (Wells Fargo): Got it. Thank you. On a related point, does dose selection read through directly from Parkinson to PSP, you think?

Speaker #4: So we think it's very related. Let's look. What both diseases share here is that they both have a toxic gain-of-function mutation that's associated with the disease or disease severity.

Noah Berkowitz: We think it's very related. You know, let's look, what both diseases share here are, they both have a toxic gain-of-function mutation that's associated with the disease or disease severity, right? We understand how there is a pathway that is activated for what, you know, and this is the endolysosomal trafficking pathway, of which LRRK2 plays a central role. Our goal, as was stated earlier, is to degrade LRRK2 to more, you know, to at least 50%. We know that that could be achieved in both of these diseases. You know, we have reason to believe that that can direct benefit.

Speaker #4: Right? And we understand how there is a pathway that is activated for and this is the endolysosomal trafficking pathway of which LARC2 plays a central role.

Speaker #4: So, our goal, as was stated earlier, is to degrade LARC2 to at least 50%. We know that that could be achieved in both of these diseases.

Speaker #4: We have reason to believe that that can direct benefit. We've done and we've shared earlier on different calls or publications that we have that we've been able to do seeding experiments in PSP that show that LARC2 degradation can interfere with the propagation of 4R tau polymerization.

Noah Berkowitz: We've done, and we've shared earlier on different calls or publications, that we have, that we've been able to do seeding experiments in PSP that show that LRRK2 degradation can interfere with the propagation of for our tau polymerization. you know, and overall, we're going into this disease where no doubt LRRK2 has a central role, for our tau is the pathological tau species that is almost pathognomonic for the disease, right? I mean, it's found in all patients with PSP on autopsy, and we know that we should be able to degrade this tau or prevent its accumulation.

Speaker #4: And in overall, we're going into this disease where no doubt LARC2 has a central role. 4R tau is the pathological tau species that is almost pathognomonic for the disease.

Speaker #4: Right? I mean, it's found in all patients with PSP on autopsy. And we know that we should be able to degrade this tau or prevent its accumulation.

Speaker #1: Great. Thank you.

Randy Teel: Great. Thank you.

Speaker #4: Sure.

Noah Berkowitz: Sure.

Speaker #1: And your next question comes from the line of Lee Watsak with Cantor Lee. Please go ahead.

Operator: Your next question comes from the line of Liisa Colby with Cantor. Liisa, please go ahead.

Speaker #6: Hey, this is Tanya Brunder on for Lee. Thanks for taking our question. We were wondering if you could shed a little bit of light on the ARV-393 data that you're planning to share in the second half of this year.

Daniel Brondron: Hey, this is Daniel Brondron for Lee. Thanks for taking our question. We were wondering if you could shed a little bit of light on the ARV-393 data that you're planning to share in the second half of this year. You've already said that there are early evidence of efficacy. What gives you confidence in your data and the molecule itself, that it is, you know, worth pursuing? What kind of data, what type of end should we be expecting in your presentation?

[Analyst] (Cantor Fitzgerald): Hey, this is Daniel Brondron for Lee. Thanks for taking our question. We were wondering if you could shed a little bit of light on the ARV-393 data that you're planning to share in the second half of this year. You've already said that there are early evidence of efficacy. What gives you confidence in your data and the molecule itself, that it is, you know, worth pursuing? What kind of data, what type of end should we be expecting in your presentation?

Speaker #6: You've already said that there is early evidence of efficacy. What gives you confidence in your data and the molecule itself—that it is worth pursuing? And what kind of data, what type of end should we be expecting in your presentation?

Speaker #3: Yeah, I'll let Noah comment, but you're right to re-highlight that late last year we said that even at doses that were below what we would have expected to produce an efficacious range of exposure, we did see some responses in patients with both B or T cell lymphomas.

Randy Teel: Yeah, I'll let Noah comment, but you're right to re-highlight that late last year, we said that even at doses that were below what we would have expected to produce an efficacious range of exposure, we did see some responses in patients with both B-cell or T-cell lymphomas and had seen good degradation with BCL6. For the data later in the year, Noah?

Speaker #3: And had seen good degradation with BCL6. But for the data later in the year, Noah?

Speaker #4: Yeah. I don't think that we could guide specifically to those findings, other than to say that if you're in the business of drug development and you have a new mechanism of action, and you see a drug that can achieve a complete metabolic response in patients that otherwise have a deadly disease, you remain very committed and enthusiastic about the future for that product.

Noah Berkowitz: Yeah. I don't think that we could guide specifically to those findings other than to say that if you're in the business of drug development and you have a new mechanism of action, and you see a drug that can achieve a complete metabolic response in patients that otherwise have a deadly disease, you remain very committed and enthusiastic about the future for that product.

Speaker #1: And your next question comes from the line of Crepa de Varaconda with TURI Securities. Crepa, please go ahead.

Operator: Your next question comes from the line of Srikripa Devarakonda with Truist Securities. Kripa, please go ahead.

Speaker #5: Hi, good morning. This is Anna on for Crepa. A couple of questions for me. Jumping to the polyQAR degrader, just given that SBMA is kind of a progressive disease and an untapped market, I know it's still an early program, but I was wondering if there's anything you can any guidance you can give in terms of the strategy here and if there's anything you'll be testing in the future that can kind of support any early signs of efficacy and additionally for 806, wondering if there's any early indications of any interest within pancreatic colorectal or lung cancer.

[Analyst] (Truist Securities): Hi, good morning. This is Anna on for Kripa. A couple of questions from me. Jumping to the polyQ-AR degrader, just given that SBMA is kind of a progressive disease and an untapped market, I know it's still an early program, but I was wondering if there's anything you can, any guidance you can give on, in terms of the strategy there. If there's anything you'll be testing in this phase 1 that can kind of support any early signs of efficacy. Additionally, for ARV-806, wondering if there's any early indications of any interest within pancreatic, colorectal, or lung cancer. Thank you.

Srikripa Devarakonda: Hi, good morning. This is Anna on for Kripa. A couple of questions from me. Jumping to the polyQ-AR degrader, just given that SBMA is kind of a progressive disease and an untapped market, I know it's still an early program, but I was wondering if there's anything you can, any guidance you can give on, in terms of the strategy there. If there's anything you'll be testing in this phase 1 that can kind of support any early signs of efficacy. Additionally, for ARV-806, wondering if there's any early indications of any interest within pancreatic, colorectal, or lung cancer. Thank you.

Speaker #5: Thank you.

Speaker #4: Okay.

Randy Teel: Okay. Yeah, we'll do O 27 first, Noah and Angela, and then come back.

Speaker #3: Yeah. We'll do 027 first. Noah and Angela, and then come back.

Speaker #4: Yes. I'm going to start almost at the end and then turn it back to Angela because it will have to do with clinical strategy.

Noah Berkowitz: Yes. I'm going to start, like, almost at the end and then turn it back to Angela because it will have to do with clinical strategy. Which is to say it's really early, so I can't answer the question in great detail there, but I'll give you a range of possibility, right? We already know that patients with SBMA show a pattern of muscle atrophy and fat infiltration that can be picked up clearly with the right sequencing on MRI. That is a setup for a surrogate marker for the disease. Surrogacy requires significant engagement with health authorities and, you know, a review of the data that is out there existing and possibly new, and negotiation. We're at the very beginning of a process, but knowing that that is potentially something that we could look at in the future.

Speaker #4: Which is to say, it's really early, so I can't answer the question in great detail. But I'll give you a range of possibility. Right?

Speaker #4: We already know that patients with SBMA show a pattern of muscle atrophy and fat infiltration that can be picked up clearly with the right sequencing on MRI.

Speaker #4: So that is a setup for a surrogate marker for the disease. But surrogacy requires significant engagement with health authorities and a review of the data that is out there existing and possibly new.

Speaker #4: And negotiation. So we're at the very beginning of a process, but knowing that that is potentially something that we could look at in the future.

Speaker #4: Beyond that, we know that if you're not going to rely on surrogacy, you're going to look at things like a six-minute walk test or other functional measure of patient strength and their ability to not deteriorate.

Noah Berkowitz: Beyond that, we know that, if you're not going to rely on surrogacy, you're going to look at things like a six-minute walk test or other functional measure of patient strength and their ability to not deteriorate, right? Because ultimately, these patients become bedbound, they develop bulbar symptoms, they, you know, it does happen over the course of many years, but it is progressive and it's trackable. That's the strategy. I think those are things we're looking at in that range, and I'll turn it to Angela.

Speaker #4: Right? Because ultimately, these patients become bedbound. They develop bulbar symptoms. It does happen over the course of many years, but it is progressive and it's trackable.

Speaker #4: So that's the strategy. I think those are things we're looking at in that range. And I'll turn it to Angela to share.

Angela Cacace: Great.

Angela M. Cacace: Great.

Noah Berkowitz: Sure.

Speaker #5: Great. Okay. So, preclinically, we've been degrading the root cause of spinal and bulbar muscular atrophy, which is the polyglutamine repeat expanded androgen receptor in muscle, as the goal of the program.

Angela Cacace: Okay. Preclinically, you know, we've, you know, degrading the root cause of spinal-bulbar muscular atrophy, which is the polyglutamine-repeated, expanded androgen receptor in muscle, is the goal of the program. We've been able to do that with ARV-027. In the preclinical models, we see very robust reduction in muscle, and this leads to, you know, improvement in muscle atrophy. We see increased grip strength, we see improved endurance, and all of these things lead to improved muscle energetics, and we can measure these things in terms of muscle biopsy, right?

Angela M. Cacace: Okay. Preclinically, you know, we've, you know, degrading the root cause of spinal-bulbar muscular atrophy, which is the polyglutamine-repeated, expanded androgen receptor in muscle, is the goal of the program. We've been able to do that with ARV-027. In the preclinical models, we see very robust reduction in muscle, and this leads to, you know, improvement in muscle atrophy. We see increased grip strength, we see improved endurance, and all of these things lead to improved muscle energetics, and we can measure these things in terms of muscle biopsy, right?

Speaker #5: And so we've been able to do that with ARV027. And in the preclinical models, we see very robust reduction in muscle. And this leads to improvement in muscle atrophy.

Speaker #5: We see increased grip strength. We see improved endurance. And all of these things lead to improved muscle energetics. And we can measure these things in terms of muscle biopsy.

Speaker #5: Right? So the goal of the preclinical program, and turning it into a translational program, is to measure the reductions that we see in our healthy volunteers, and then ultimately in the Phase 1 trial, to include SBMA patients also and measure muscle biopsy for reduction of AR, and then polyQ AR, and then ultimately, as Noah was saying, relate that to measures of muscle atrophy, which can then be measured as muscle integrity measures, which are muscle MRI.

Angela Cacace: The goal of the preclinical program and turning into a translational program is to measure the reductions that we see in our healthy volunteer, and then ultimately, in the phase 1 trial, is to include SBMA patients also and measure muscle biopsy for reduction of AR and then polyQ-AR. Ultimately, as Noah was saying, relate that to measures of, you know, muscle atrophy, which can be then measured as muscle integrity measures, which are muscle MRI. Fat infiltration, muscle fat volume, things like muscle volume, et cetera, and then function.

Angela M. Cacace: The goal of the preclinical program and turning into a translational program is to measure the reductions that we see in our healthy volunteer, and then ultimately, in the phase 1 trial, is to include SBMA patients also and measure muscle biopsy for reduction of AR and then polyQ-AR. Ultimately, as Noah was saying, relate that to measures of, you know, muscle atrophy, which can be then measured as muscle integrity measures, which are muscle MRI. Fat infiltration, muscle fat volume, things like muscle volume, et cetera, and then function.

Speaker #5: So, fat infiltration, muscle fat volume, things like muscle volume, etc. And then function. So, yeah.

Speaker #3: Then maybe I'll rewind one more click before we get too back to the key rest question. But just as a reminder for everybody, this is the third AR degrader we put in the clinic.

Randy Teel: maybe I'll rewind one more click before we get back to the KRAS question. just as a reminder for everybody, this is the third AR degrader we put in the clinic. bavdegalutamide was our first years ago, one of the first, well, the first PROTAC we put into the clinic, which had some solid signals of efficacy and good tolerability early on. The next generation AR degrader was 766, which we outlicensed to Novartis about 2 years ago for upwards of $1 billion in upfront and milestones. just wanted to make sure that's clear. AR is an area where we have deep expertise we'll take advantage of. Now, back to your the second question, which was around KRAS. Could you please remind me what the question was?

Speaker #3: So Babdigalutamide was our first years ago one of the first the first PROTAC we put into the clinic. Which had some solid signals of efficacy and good tolerability early on.

Speaker #3: The next generation AR degrader was 766, which we outliced to Novartis about two years ago for upwards of a billion dollars in upfront and milestones.

Speaker #3: So, I just wanted to make sure that's clear. AR is an area where we have deep expertise, which we'll take advantage of. Now, back to the second question, which was around KRAS.

Speaker #3: Could you please remind me what the question was? I think it was about moving into PDAC, but what was the question, please?

Randy Teel: I think it was about moving into PDAC, but what was the question, please?

Speaker #5: Yeah. Just any early indications within PDAC colorectal versus lung?

[Analyst] (Goldman Sachs): Yeah, just any early indications within PDAC, colorectal versus lung?

Speaker #3: Any indications? You mean in terms of development direction?

Randy Teel: Any indications? You mean in terms of development direction?

[Analyst] (Goldman Sachs): Any early indications of interest, yeah.

Speaker #5: Any early indications of interest? Yeah.

Noah Berkowitz: Well, clinical trial, I don't think we're gonna share where the program is, but other than to say that it's moved faster than expected, which I think we just mentioned on the call. Beyond that, we've already submitted for a conference. We'll see what, you know, how this plays out.

Speaker #4: So clinical trial, I don't think we're going to share where the program is, but we other than to say that it's moved faster than expected, which I think we just mentioned on the call.

Speaker #4: And beyond that, that we've already submitted for a conference. So we'll see what right now how this plays out.

Speaker #3: So lots of things of interest. Yeah.

Randy Teel: Lots of great interest today. Yeah.

Speaker #5: Thank you so much.

[Analyst] (Goldman Sachs): Thank you so much.

Randy Teel: Thank you.

Speaker #1: And your next question comes PTIG. Jade, please go ahead.

Operator: Your next question comes from the line of Jeet Mukherjee with BTIG. Jeet, please go ahead.

Speaker #6: Hey, this is Blake Gunn for Jade's. You started getting into this earlier, but how do you think about the pancrest program coexisting with 806 and specifically is pancrest designed to cover other variants besides for G12D, or could it with a clean therapeutic window eventually replace 806 entirely?

[Analyst] (BTIG): Hey, this is Blake on for Jeet. You started getting into this earlier, but how do you think about the pan-KRAS program coexisting with ARV-806? Specifically, is pan-KRAS designed to cover other variants besides for G12D, or could it, with a clean therapeutic window, eventually replace ARV-806 entirely? Thank you.

Blake Ray: Hey, this is Blake on for Jeet. You started getting into this earlier, but how do you think about the pan-KRAS program coexisting with ARV-806? Specifically, is pan-KRAS designed to cover other variants besides for G12D, or could it, with a clean therapeutic window, eventually replace ARV-806 entirely? Thank you.

Speaker #6: Thank you.

Speaker #3: Yeah. It's a good question. Right? So G12D very specifically targets G12D, whereas the pan-KRAS is intended to target all the mutants for sure. In terms of how they can coexist, maybe I'll make a high-level comment and then pass to Noah.

Randy Teel: Yeah, it's a good question, right? G12D very specifically targets G12D, whereas the pan KRAS is intended to target all the mutants for sure. In terms of how they can coexist, you know, maybe I'll make a high-level comment and then pass to Noah. In general, we've seen them as independent programs, right? There is certainly argument to say that a specific G12D degrader could have a profile that better allows for combination with other therapies. That's theoretical for sure. A pan KRAS degrader that had a great tolerability profile could be quite combinable as well. We have seen them as independent programs. Noah, anything else you'd like to add on how they could move forward?

Speaker #3: But in general, we've seen them as independent programs. Right? There is certainly argument to say that a specific G12D degrader could have a profile that better allows for combination with other therapies.

Speaker #3: That's theoretical for sure. A pan-KRAS degrader that had a great tolerability profile could be quite combinable as well. So we have seen them as independent programs.

Speaker #3: Noah, anything else you'd like to add on how they could move forward?

Noah Berkowitz: Yeah, I think that that's the key point. We've highlighted before that one of the key mechanisms that differentiates degraders from inhibitors is our ability to continue to degrade in the press, in the presence of amplification or overexpression. That's something that the pan-KRAS degrader would be poised to add. I think that, you know, as you know, there's probably about 35%, 40% of pancreatic cancer patients have G12D. That leaves the other 55%, you know, or 50% of patients that have other variants. They're just in pancreatic cancer alone, there is a larger opportunity for a pan-KRAS than a G12D. Differentiation, you know, we like the idea of potentially using them together, and we like the idea of being able to really overcome resistance pathways.

Speaker #4: Yeah. I think that's the key point. We've highlighted before that one of the key mechanisms that differentiates degraders from inhibitors is our ability to continue to degrade in the presence of amplification or overexpression.

Speaker #4: So that's something that the pan-KRAS degrader would be poised to add. I think that as you know, there's probably about 35, 40 percent of pancreatic cancer patients have G12D.

Speaker #4: But that leaves the other 55 or 50 percent of patients that have other variants. So they're just in pancreatic cancer alone, there is a larger opportunity for a pan-KRAS than a G12D.

Speaker #4: Differentiation, we like the idea of potentially using them together. And we like the idea of being able to really overcome resistance pathways. So that's it.

Noah Berkowitz: That's it. That same pattern, though to smaller percentages, is true in non-small cell lung cancer, in colorectal cancer, and potentially in other GI tumors as well.

Speaker #4: And that same pattern, though to smaller percentages, is true in non-small cell lung cancer, in colorectal cancer, and in other potentially in other GI tumors as well.

Speaker #1: Thank you. And your next question comes from the line of Terence Flynn with Morgan Stanley. Terence, please go ahead.

[Analyst] (BTIG): Thank you.

Blake Ray: Thank you.

Operator: Your next question comes from the line of Terence Flynn with Morgan Stanley. Terence, please go ahead.

Speaker #7: Great. Thanks for taking the question. Randy, you talked a lot about the opportunity set this year from a lot of the early-stage programs in terms of data.

Terence Flynn: Great. Thanks for taking the question. Randy, you talked a lot about, you know, the opportunity set this year from a lot of the early-stage programs in terms of data. How are you thinking about potential partnerships for these programs? I know historically you have kept some, you've partnered others, how are you thinking about partnering versus retaining rights on each of these? Thank you.

Speaker #7: How are you thinking about potential partnerships for these programs? I know historically you have kept some. You've partnered others. So how are you thinking about partnering versus retaining rights on each of these?

Speaker #7: Thank you.

Speaker #3: Yeah. It's a great question, Terence. Thanks. And I think stepping up a little bit, right, what we've done here is we've got a platform and a team that has produced some really high-quality clinical candidates that we think could be differentiated.

Randy Teel: Yeah, it's a great question, Terence Flynn. Thanks. I think, you know, stepping up a little bit, right? What we've done here is we've got a platform and a team that has produced some really high-quality clinical candidates that we think could be differentiated. You know, we've got 3 in the clinic, as we announced this morning, 4 now, just very recently with ARV-207 going in, and ARV-6723 for HPK1, entering the clinic later in the year. That's 5, right? That is a lot for a small biotech to take on. That's what's, that's helping the strategy shift from talking about this, the fantastic platform that we have, to adding on the need for each program to be, you know, independently valued and differentiated from its competition.

Speaker #3: We've got—I was about to say three in the clinic, but as we announced this morning, four now, just very recently with 027 going in, and 6723 for HPK1 entering the clinic later in the year.

Speaker #3: So that's five. Right? That is a lot for a small biotech to take on. And so that's what's helping the strategy shift from talking about the fantastic platform that we have to adding on the need for each program to be independently valued and differentiated from its competition.

Speaker #3: And I think that as we move those programs forward, this year and beyond—not necessarily this year, right, but going forward—we may reach places where we decide that it makes sense for us to resource programs, and where it might make sense for others to.

Randy Teel: I think that as we move those programs forward this year and beyond, not necessarily this year, right, but going forward, we may reach places where we decide that it makes sense for us to resource programs and where it might make sense for others too. You alluded to our history, right? We did a deal with Pfizer for VET back in 2021. I mentioned the luxdegalutamide deal from Novartis in 2024. Partnering certainly has been an important part of our strategy in the past and will be going, you know, forward in the future.

Speaker #3: You alluded to our history, right? We did a deal with Pfizer for vet back in 2021. I mentioned the Luxteg allutamide deal from Novartis in 2024.

Speaker #3: And so partnering certainly has been important part of our strategy in the past and will be going forward in the future. As far as program by program, we try to make sure that pharma companies are apprised of our progress across the pipeline so that we know if and when it comes time for us to look for a partner, we know who that might be.

Randy Teel: You know, as far as program by program, you know, we try to make sure that pharma companies are apprised of our progress across the pipeline, so that we know if and when it comes time for us to look for a partner, we know who that might be. I'll probably save any more specific comments for the future, but it's certainly on our mind to think about how we can best move forward each program.

Speaker #3: So I'll probably save any more specific comments for the future, but it's certainly on our mind to think about how we can best move forward each program.

Speaker #1: And your next question comes from the line of Paul Choi with Goldman Sachs. Paul, please go ahead.

Operator: Your next question comes from the line of Paul Choi with Goldman Sachs. Paul, please go ahead.

Speaker #8: Hi. This is Daniel for Paul. So two questions for us on this final bubble muscular dystrophy program. So could you guide us on what's the expected timeline for the next planned data cut?

[Analyst] (Goldman Sachs): Hi, this is Daniel on for Paul. Two questions for us on the spinal-bulbar muscular atrophy program. Could you guide us on what's the expected timeline for the next planned data cut? What type of data should we expect from the healthy volunteer study that could help de-risk the program?

Speaker #8: And what type of data should we expect from the healthy volunteer study that could help de-risk the program, including that could there be muscle biopsy for measuring intracellular AR concentrations?

[Analyst] (Goldman Sachs): ... including that could there be muscle biopsy for measuring intracellular AR concentrations? Thank you very much.

Speaker #8: Thank you very much.

Speaker #3: Sure. Why don't I take the first one because it's easy, and I'll pass to the team for the second one. With respect to the timeline, we've said we just started in the clinic just now.

Randy Teel: Sure. Why don't I take the first one, 'cause it's easy, and I'll pass to the team for the second one. With respect to the timeline, we've said we just started in the clinic just now. A bit early to guide on when we'll see our first data, so I would not anticipate that in the very near future. As that study gets up and running, we'll look to provide some guidance on that. We've spoken a bit about the data coming from ARV-027, but yeah, and Noah, please jump in on what we can show for the healthy volunteers.

Speaker #3: So a bit early to guide on when we'll see our first data, so I would not anticipate that in the very near future. But as that study gets up and running, we'll look to provide some guidance on that.

Speaker #3: We've spoken a bit about the data coming from 027, but Noah, please jump in on what we can show from the healthy volunteers.

Speaker #4: Sure. A classic healthy volunteer study, but it has a component that we'll follow up in the end with some SBMA patients. So think of it as your initial establishing the dose range, right, in a dose-escalating single-ascending dose treatment of patients.

Noah Berkowitz: A classic healthy volunteer study, but it has a component that, you know, we'll follow up in the end with some SBMA patients. Think of it as your initial establishing the dose range, right? In a dose-escalating single ascending dose treatment of patients. That drives then to multiple ascending dose cohorts. We'll be looking at PK. There is a PD component here that is very strong, that we don't have in many other studies. The PD here is we're targeting AR degradation and AR degradation in muscle, and we can biopsy those muscles, and we will. That will help us choose the right dose range to move forward into later trials. We are not guiding yet to...

Speaker #4: That drives them to multiple ascending dose cohorts. We'll be looking at PK; there is a PD component here that is very strong, which we don't have in many other studies.

Speaker #4: The PD here is we're targeting AR degradation and AR degradation in muscle. And we can biopsy those muscles, and we will. And that will help us choose the right dose range to move forward into later trials.

Speaker #4: We are not guiding yet to—and by the way, so that's both for the healthy volunteers and the SAD and MAD, but then in this confirmatory small cohort of SBMA patients at the end, we'll also be doing those biopsies.

Noah Berkowitz: By the way, that's both for the healthy volunteers and the SAD and MAD, in, like, this confirmatory small cohort of SBMA patients at the end, we'll also be doing those biopsies. I don't think we can guide right now to when we'll have those results, since we just recently dosed our first patients, we'll keep you updated.

Speaker #4: We just aren't—I don't think we can guide right now to when we'll have those results, but we'll—since we just recently dosed our first patients.

Speaker #4: But we'll keep you updated.

Speaker #8: Thank you.

[Analyst] (Goldman Sachs): Thank you.

Speaker #1: And your next question comes from the line of Michael Smith with Guggenheim Securities. Michael, please go ahead.

Operator: Your next question comes from the line of Michael Schmidt with Guggenheim Securities. Michael, please go ahead.

Speaker #9: Hey, this is Sarah on from Michael. Thanks so much for taking my question. I wanted to circle back to the pan-KRAS degrader. So you've spoken a lot about the preclinical data that you've seen, but wanted to ask when you might expect it to be IND ready.

[Analyst] (Guggenheim Securities): Hey, this is Sarah on for Michael. Thanks so much for taking my question. I wanted to circle back to the pan KRAS activator. You've spoken a lot about the preclinical data that you've seen, but wanted to ask when you might expect it to be IND ready. As well, you know, what your current view on the opportunity is in pan KRAS, given that I believe we've recently seen, you know, first clinical data from another pan KRAS agent. Thank you.

Speaker #9: And then as well, what your current view on the opportunity is in pan-KRAS, given that I believe we've recently seen first clinical data from another pan-KRAS agent.

Speaker #9: Thank you.

Speaker #3: Yeah. We haven't talked yet about the exact timing for the clinic for pan-KRAS, so won't give that guidance quite yet. But although, as you can see, we're continuing to put out data at multiple conferences there.

Randy Teel: We haven't talked yet about the exact timing for the clinic for pan-KRAS, won't give that guidance quite yet. Although, as you can see, we're continuing to put out data at multiple conferences there, it's moving ahead well. In terms of the opportunity for pan-KRAS, you're right that there's other programs in this space for sure. Going back to the questions from, especially from John at the start, it's a place where we're certainly gonna have to be differentiated, but we think that space is one where having multiple programs across G12D and pan will be helpful. Combinations with those and other agents will be important as we move forward. Anything else, Noah, that you'd like to add?

Speaker #3: So it's moving ahead well. In terms of the opportunity for pan-KRAS, you're right that there's other programs in the space for sure. Going back to the questions from especially from John at the start, it's a place where we're certainly going to have to be differentiated.

Speaker #3: But we think that space is one where having multiple programs across G12D and pan will be helpful. Combinations with those and other agents will be important as we move forward.

Speaker #3: Anything else? Noah, that you'd like to add? I think we've—I think we've said what we can on the pan-KRAS opportunity for now.

Randy Teel: I think we've said what we can on the pan-KRAS opportunity for now.

Speaker #9: Got it. Thank you.

[Analyst] (Guggenheim Securities): Got it. Thank you.

Speaker #1: And your next question comes from the line of Suzanne Logan-Oven with Stevens, Inc. Suzanne, please go ahead.

Operator: Your next question comes from the line of Sudan Loganathan with Stephens Inc. Sudan, please go ahead.

Speaker #10: Hi. Thank you. First, wanted to say congrats to Randy for his continuing on ARVINAS with this new role. Looking forward to working with you and the team as ARVINAS kind of takes on this plethora of exciting new projects.

Sudan Loganathan: Hi, thank you. First wanted to say, congrats to Randy for his continuing on at Arvinas with his new role. Looking forward to working with you and the team as Arvinas kind of takes on this plethora of exciting new projects. My first question is, you know, as you move towards initiating the Phase 1b in PSP, what specific regulatory feedback are you seeking from the agency? Separately, is there any risk that regulatory feedback in PSP alters the development strategy or timelines for the PD program? Then finally, can you outline how you're thinking about the trial design evolution in both PSP and PD endpoints, enrichment strategy, duration, and what constitutes registrational credibility dataset in each indication?

Sunil Loganathan: Hi, thank you. First wanted to say, congrats to Randy for his continuing on at Arvinas with his new role. Looking forward to working with you and the team as Arvinas kind of takes on this plethora of exciting new projects. My first question is, you know, as you move towards initiating the Phase 1b in PSP, what specific regulatory feedback are you seeking from the agency? Separately, is there any risk that regulatory feedback in PSP alters the development strategy or timelines for the PD program? Then finally, can you outline how you're thinking about the trial design evolution in both PSP and PD endpoints, enrichment strategy, duration, and what constitutes registrational credibility dataset in each indication?

Speaker #10: My first question is, as you move towards initiating the phase 1B and PSP, what specific regulatory feedback are you seeking from the agency? Separately, is there any risk that regulatory feedback in PSP alters the development strategy or timelines for the PD program?

Speaker #10: And then finally, can you outline how you're thinking about the trial design evolution in both PSP and PD endpoints? Enrichment strategy, duration, and what constitutes registrational credibility set in each indication.

Speaker #3: Right. Okay. Thanks for the multiple questions there, and thanks for the comments. Look to get the phase 1B started. It's your fairly typical moving it through the regulatory authorities.

Randy Teel: Right. Okay, thanks for the multiple questions there, and thanks for the comments. Look, to get to Phase 1b started, it's your fairly typical moving it through the regulatory authorities. You know, with our guidance of starting that in the first half of the year, you can presume we're moving forward there, and all is on track. With respect to, you know, data for PD versus PD, PSP, Noah, I'll ask you to comment there in terms of, you know, how the development could affect each program.

Speaker #3: With our guidance of starting that in the first half of the year, you can presume we're moving forward there. And all is on track.

Speaker #3: With respect to data for PD versus PSP, Noah, I'll ask you to comment there in terms of the development could affect each program.

Speaker #4: Right. So in terms of the question, there are two questions there, right? What is the—how can the regulatory feedback impact both programs? And then there were questions about enrichment strategy and things like that.

Noah Berkowitz: Right. In terms of... The question was, Well, there are two questions there, right? What is the, how can the regulatory feedback impact both programs? Then there were questions about enrichment strategy and things like that. There's no, we're just filing the IND, right? Even though we did all this work outside of the US, we haven't interacted with the FDA. There's an opportunity here, and I think it's more opportunity rather than risk, right? To speak to the FDA about these plans. Think of our IND as mapping out what we expect to do with our development, you know, with the first trial, and opening up this dialogue, because the FDA knows a lot about PSP and PD, and we're hoping to get really good feedback.

Speaker #4: So there's no—we're just filing the IND, right? So even though we did all this work outside of the US, we haven't interacted with the FDA.

Speaker #4: And so there's an opportunity here—and I think it's more opportunity rather than risk, right?—to speak to the FDA about these plans. So think of our IND as mapping out what we expect to do with our development, with the first trial, and opening up this dialogue because the FDA knows a lot about PSP and PD.

Speaker #4: And we're hoping to get really good feedback. There are—the risk-benefit of drugs developed in PSP and Parkinson's disease are different. So we're going to start off with PSP.

Noah Berkowitz: There are, the risk-benefit of drugs developed in PSP and Parkinson's disease are different. We're gonna start off with PSP. You know, the intent is to eventually have a conversation about Parkinson's disease also. I don't think that we're gonna go into details on a call here about the Parkinson's development strategy, because we've only guided towards what we're doing in PSP today. Suffice it to say, once we clear these discussions with PSP, the idea would be to start moving into conversations around Parkinson's disease. You raised the question about what could enrichment strategy look like. In PSP, it isn't gonna be a biomarker or a biomarker enrichment, but there's gonna be a patient focus.

Speaker #4: The intent is to eventually have a conversation about Parkinson's disease also. I don't think that we're going to go into details on a call here about the Parkinson's development strategy, because we've only guided towards what we're doing in PSP today.

Speaker #4: But suffice it to say, once we clear these discussions with PSP, then the idea would be to start moving into conversations around Parkinson's disease.

Speaker #4: You raised the question about what could enrichment strategy look like. So in PSP, it isn't going to be a biomarker or a biomarker enrichment, but there's going to be a patient focus.

Speaker #4: So we'll be looking at patients that have PSPRS, the more severe and symptomatic form, and aggressive form of the disease. I don't remember exactly, but I think they probably represent about 40% of patients with PSP.

Noah Berkowitz: We'll be looking at patients that have PSP-RS, you know, the more severe and symptomatic form and aggressive form of the disease. I don't remember exactly, but I think they probably represent about 40% of patients with PSP. That would be our focus for enrollment in this in the study. We are gonna develop a strategy, and we'll guide eventually towards how this gets expanded into the broader population or even if that's necessary. In terms of Parkinson's disease, I think what folks can start anticipating is that we're doing a lot of work trying to understand what are the biomarkers that predict outcome in Parkinson's disease, using existing sources that have had major investments in a lot of publications, such as the PPMI, so the Michael J. Fox Foundation-funded Parkinson's Progression Initiative. We're using that to help identify markers.

Speaker #4: That would be our focus for enrollment in this in the study. And we are going to develop a strategy, and we'll guide eventually towards how this gets expanded into the broader population or even if that's necessary.

Speaker #4: In terms of Parkinson's disease, I think what folks can start anticipating is that we're doing a lot of work trying to understand what are the biomarkers that predict outcome in Parkinson's disease, using existing sources that have had major investment and a lot of publication, such as the PPMI, so the Michael J.

Speaker #4: Fox Foundation-funded Parkinson's Progression Initiative. And we're using that to help identify markers. Think of it, we can start now tying that into the biomarker changes that we see in our healthy volunteer study and that we're seeing in our Parkinson's disease study.

Noah Berkowitz: Think of it, we can start now tying that in to the biomarker changes that we see in our healthy volunteer study, and that we're seeing in our Parkinson's disease study. We're at a unique competitive advantage, having the only degrader being developed in this space, and having already shared, at least in healthy volunteers, that we have biomarker movement, that we could start correlating these biomarkers to prognosis in Parkinson's disease. Think of this as moving ahead into, you know, we'll do that with our Parkinson's disease patients, and eventually this may lead to some patient selection strategies or analyses we can do in our studies. Can't offer more guidance than that, but it gives you a sense of where we could be headed.

Speaker #4: So, we’re at a unique competitive advantage, having the only degrader being developed in this space. And having already shared, at least in healthy volunteers, that we have biomarker movement, we could start correlating these biomarkers to prognosis in Parkinson’s disease.

Speaker #4: And think of this as moving ahead into we'll do that with our Parkinson's disease patients and eventually this may lead to some patient selection strategies or analyses we can do in our studies.

Speaker #4: So, can't offer more guidance than that, but it gives you a sense of where we could be headed.

Speaker #1: I appreciate the details. Thank of Esther Sarod with Barclays Esther. Please go ahead.

Randy Teel: I appreciate the details. Thank you.

Operator: Our final question comes from the line of Esther Lim with Barclays. Esther, please go ahead.

Speaker #11: Hi. This is Lee John for Esther. Thanks for taking my question. For 102 and PSP, since PSP doesn't really have any disease-modifying therapies or anything, just needs to treat symptoms, what kind of clinical endpoints even early ones are you going to be looking for, and what are regular regulators looking for to really support that move into a registrational trial later this year?

[Analyst] (Barclays): Hi, this is Luke on for Esther Lim. Thanks for taking my question. For ARV-102 and PSP, since PSP, like, doesn't really have any disease-modifying therapies, everything just needs to treat symptoms, what kind of clinical endpoints, even early ones, are you gonna be looking for, and what are regular regulators looking for, to really support that move into a registrational trial later this year? For Vepdegestrant, I guess, in kind of like a worst-case scenario, if you don't have a collaboration lined up by the PDUFA, do you have a backup commercialization plan?

Speaker #11: And for VEPDEG, I guess, and kind of like a worst-case scenario, if you don't have a collaboration lined up by the PDUFA, do you have a backup commercialization plan?

Speaker #3: Maybe I'll take the second one on VEP and then pass back to Noah for PSP. Look, as I've said, we're moving ahead well on the partnership plans alongside our partners at Pfizer.

Randy Teel: Maybe I'll take the second one on Vep, and then pass back to Noah for PSP. Look, as I said, we're moving ahead well on the partnership plans alongside our partners at Pfizer. If that becomes an issue, certainly, we're well situated with Pfizer to address that question. As the process is moving along, it's less of a concern, but certainly it's something we have on the radar if needed. Noah, back to you on the PSP questions.

Speaker #3: And if that becomes an issue, certainly we're well situated with Pfizer to address that question. As the process is moving along, it's less of a concern, but certainly, it's something we have on the radar if needed.

Speaker #3: Noah, back to you on the PSP questions.

Speaker #4: Yeah, I think the gold standard in PSP, where there have been attempts to develop symptom-modifying drugs but not necessarily disease-modifying drugs, is the PSP rating scale.

Noah Berkowitz: Yeah. I think the gold standard in PSP, where there have been attempts to develop symptom modifying drugs, but not necessarily disease-modifying drugs, is the Progressive Supranuclear Palsy Rating Scale. We would intend to use that in our regulatory, I'm sorry, our, you know, submission quality study down the road. It's obviously gonna be used in the phase 1b, which is not gonna be powered to evaluate that fully, but it can identify trends between what's going on with biomarkers and that tool.

Speaker #4: So we would intend to use that in our regulatory I'm sorry, our submission quality study down the road. It's obviously going to be used in the phase 1B, which is not going to be powered to evaluate that fully, but look for but it can identify trends between what's going on with biomarkers and that tool.

Speaker #4: And something else we include in all of our studies in these neurodegenerative diseases—we did it in our Parkinson's disease, and we'll be doing similar type of work in the PSP studies, even the phase 1b—is looking at things like eye movements or other types of indicators or surrogacy for function, right?

Noah Berkowitz: Something else we include in all of our start studies in these neurodegenerative diseases, we did it in our Parkinson's disease, and we'll be doing similar type of work in the PSP studies, even the phase 1b, is looking at things like eye movements or other type of, you know, indicators or surrogacy for function, right? It's a rapidly evolving space, where there are some markers, you know, of movement in the eyes or muscle movement that may be predictive of clinical outcomes. These are not accepted as registration quality tools yet, but they're things that we're incorporating into our studies because we think they could be very revealing.

Speaker #4: It's a rapidly evolving space where there are some markers of movement in the eyes or muscle movement that may be predictive of clinical outcomes.

Speaker #4: These are not accepted as registration quality tools yet, but they're things that we're incorporating into our studies because we think they could be very revealing.

[Analyst] (Barclays): I take-

Speaker #1: That concludes our question and answer session. I will now turn the call back over to Randy Teal for closing remarks. Randy?

Operator: That concludes our question and answer session. I will now turn the call back over to Randy Teel for closing remarks. Randy?

Speaker #3: Thank you very much, Arvida. And thanks all on the call for all the good questions. I'll close by just saying that now that we've positioned ourselves as a phase 1 company, the priorities are clearly to move the trials along, produce some good data, and make decisions, right?

Randy Teel: Thank you very much, operator, and thanks all on the call for all the good questions. You know, I'll close by just saying that now that we've positioned ourselves as a phase 1 company, the priorities are clearly to move the trials along, produce some good data, and make decisions, right? As we do that over the coming months, we will look forward to keeping you all updated. Thank you all very much for joining the call.

Speaker #3: So as we do that over the coming months, we will look forward to keeping you all updated. Thank you all very much for joining the call.

Operator: That concludes today's call. You may now disconnect.

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