Suven Life Sciences Completes Phase-3 Patient Enrollment for Masupirdine Study
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Suven Life Sciences has completed enrollment in its global Phase-3 study of Masupirdine (SUVN-502) for treating agitation linked to Alzheimer's dementia. 424 patients were randomized against a target of 375 across USA and Europe, testing 50 mg and 100 mg doses against placebo over 12 weeks. Last patient visit is expected by end December 2026, database lock by March 2027, and topline results by May 2027. No safety concerns observed so far.
Key clinical milestone completed on schedule. Positive topline results by May 2027 could be a significant value driver for this CNS-focused pharma company.