
Neurocrine Biosciences' Phase 4 KINECT-PRO study of INGREZZA capsules demonstrated significant improvements in patient-reported outcomes related to physical functioning, social interactions, and emotional well-being in tardive dyskinesia patients. The open-label study, which involved flexible dosing of INGREZZA (40-80mg), showed benefits across all severity levels of the condition. The company's stock is currently trading down 0.82% at $122.01.
Neurocrine Biosciences (NBIX) announced positive data from its Phase 4 KINECT-PRO open-label study for INGREZZA capsules, specifically evaluating patient-reported outcomes in a tardive dyskinesia population reflective of real-world clinical practice. The study, which included a 24-week treatment period with flexible INGREZZA dosing (40 mg, 60 mg, or 80 mg once-daily after an initial four weeks at 40 mg), demonstrated robust and clinically meaningful improvements in patients' physical functioning, social interactions, and emotional well-being. Significantly, these positive outcomes were observed across all severity levels of tardive dyskinesia, highlighting INGREZZA's benefit even for individuals with milder uncontrolled movements who reported negative impacts at baseline. These findings, presented at the 2025 Psych Congress Elevate, reinforce the therapeutic value of INGREZZA in a broader patient context. Despite this encouraging clinical news, indicated by a "strongly positive" sentiment score of 0.65 and an NBIX-specific sentiment of 0.8, the company's stock is currently trading at $122.01, down 0.82 percent on the Nasdaq.
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