Clinical Trial

Evaluating Safety and Efficacy of VV119 in Acute Schizophrenia Adults

Not Yet Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
This will be a multicenter, randomized, double-blind, placebo and active comparator parallel-controlled study designed to assess the safety and efficacy of VV119 (2.0 to 6.0 mg) for the treatment of adult participants diagnosed with DSM-5 schizophrenia who are in an acute exacerbation phase.
Trial Details
NCT Number NCT07703956
Lead Sponsor Vigonvita Life Sciences
Conditions Schizophrenia
Enrollment 500 participants
Start Date 2026-07-31
Primary Completion 2027-10-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-15