Clinical Trial

A Phase 2 Study to Evaluate the Efficacy and Safety of LY03020 in Acutely Psychotic Participants With Schizophrenia

Not Yet Recruiting Phase 2
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Summary
This is a multicenter, randomized, double-blind, parallel-group, placebo-controlled, fixed-dosed phase II clinical study to evaluate the efficacy and safety of LY03020 in chinese acutely psychotic adult subjects with schizophrenia.
Trial Details
NCT Number NCT07396870
Lead Sponsor Luye Pharma Group Ltd.
Conditions Schizophrenia
Enrollment 160 participants
Start Date 2026-03-31
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-09