Clinical Trial

Compare the Efficacy and Safety of KH607 Tablets Versus Vortioxetine Hydrobromide Tablets in Adult Patients With Major Depressive Disorder

Not Yet Recruiting Phase 3
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Summary
This trial includes a short-term study and a long-term study. The short-term study is a multicenter, randomized, double-Blind, double-Dummy, Parallel-Controlled study with a 6-week duration. The long-term study is a withdrawal follow-up study; participants meeting relapse criteria may receive one cycle of KH607 Tablets treatment.
Trial Details
NCT Number NCT07741331
Lead Sponsor Chengdu Kanghong Pharmaceutical Group Co., Ltd.
Conditions Major Depressive Disorder (MDD)
Enrollment 326 participants
Start Date 2026-07
Primary Completion 2027-12 (estimated)
Study Completion 2028-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-03