Rapport Therapeutics, Inc. ((RAPP)) announced an update on their ongoing clinical study.
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Study Overview: Rapport Therapeutics, Inc. is conducting a Phase 2 clinical study titled A Phase 2, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of RAP-219 for the Acute Treatment of Manic Episodes, With or Without Mixed Features, Associated With Bipolar I Disorder. The key objective is to assess the safety and effectiveness of RAP-219 in treating mania in adults with bipolar I disorder, a condition with significant impact on mental health and quality of life.
Intervention/Treatment: The study tests RAP-219, an investigational drug administered orally once daily for 21 days, against a placebo. RAP-219 aims to alleviate manic episodes in bipolar I disorder patients.
Study Design: This interventional study is randomized and uses a parallel assignment model. It is quadruple-masked, meaning participants, care providers, investigators, and outcomes assessors are unaware of the treatment allocations. The primary purpose is treatment-focused, comparing RAP-219 with a placebo.
Study Timeline: The study began on May 30, 2025, with the latest update on October 8, 2025. These dates are crucial as they indicate the study’s progress and ongoing recruitment status.
Market Implications: The successful development of RAP-219 could positively impact Rapport Therapeutics’ stock performance, given the high demand for effective bipolar disorder treatments. Investors should monitor this study’s progress, as favorable results could enhance the company’s competitive position in the mental health treatment market.
The study is ongoing, with further details available on the ClinicalTrials portal.