Neumora Therapeutics (NMRA) Status Update summary
Event summary combining transcript, slides, and related documents.
Status Update summary
20 Jan, 2026Program overview and clinical rationale
Navacaprant is a highly selective, once-daily kappa-opioid receptor antagonist developed as a monotherapy for major depressive disorder (MDD) and other neuropsychiatric conditions, with a favorable safety and tolerability profile in phase II studies.
Phase II data showed significant improvements in depressive symptoms and anhedonia, with no weight gain, sexual dysfunction, or other common antidepressant side effects.
The COASTAL Program consists of three replicate phase III studies (COASTAL-1, -2, -3) and a long-term safety extension, all designed to maximize the probability of regulatory success.
The primary endpoint is change in MADRS score at week six, with key secondary endpoints including the SHAPS for anhedonia, aligning with FDA guidance for MDD studies.
Top-line data from COASTAL-1 is expected in Q4, with additional readouts and a potential NDA submission in 2025.
Differentiation and competitive landscape
Navacaprant demonstrates over 300-fold selectivity for kappa-opioid receptors versus mu-opioid receptors, potentially enabling higher dosing and fewer side effects compared to other KORAs like aticaprant and icalcaprant.
Unlike aticaprant, which is studied as adjunctive therapy, navacaprant is being evaluated as monotherapy, offering greater clinical flexibility.
The robust safety profile and lack of abuse potential have been confirmed by FDA feedback, with no requirement for further abuse liability studies.
Clinical trial design and execution
The COASTAL studies employ rigorous patient and site selection, central raters, video compliance monitoring, and real-time data oversight to minimize placebo response and ensure data integrity.
Studies are powered at approximately 90% for the primary outcome, with measures in place to intervene quickly if inconsistencies or compliance issues are detected.
The design includes measures to ensure stability of depressive symptoms at baseline and minimize expectation bias.
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