Novartis is acquiring Tourmaline Bio for $1.4 billion, a strategic move following Tourmaline's recent announcement of promising Phase 2 results for its cardiovascular drug, pacibekitug. The drug demonstrated significant reductions in high-sensitivity C-reactive protein (hs-CRP), including a median 85% reduction after 90 days, and offers a potential quarterly dosing advantage over competitors like Novo Nordisk's ziltivekimab. This acquisition provides Novartis with a key cardiometabolic asset, while Tourmaline Bio's shares surged 58% on the news.
Novartis (NVS) has agreed to acquire Tourmaline Bio (TRML) for $1.4 billion, a strategic move driven by promising clinical data for Tourmaline's atherosclerotic cardiovascular disease drug, pacibekitug. The acquisition follows Tourmaline's recent announcement that quarterly doses of the drug led to a median 85% reduction in high-sensitivity C-reactive protein (hs-CRP) after 90 days, a key inflammatory biomarker. This performance is notable as it positions pacibekitug competitively against Novo Nordisk's (NVO) ziltivekimab, which requires monthly injections, suggesting a significant dosing advantage. An analyst from Wedbush affirmed the deal's timing as logical, given the strong data and Tourmaline's plans for Phase 3 testing, and views Novartis as an ideal partner with the necessary cardiometabolic expertise. The market reacted decisively, with TRML shares surging 58% to 47.68 in premarket trading, while NVS shares experienced a fractional decline to 128.30, a common reaction for an acquiring company.
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