drugset / Trial / NCT06828887

Dose-Finding Clinical Trial to Evaluate the Efficacy and Safety of LV232 Capsules in the Treatment of MDD

NCT06828887

Phase 2 Recruiting 400 enrolled Vigonvita Life Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

This multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-finding Phase II clinical trial aimed to determine the optimal dose of LV232 capsules for treating MDD, evaluate preliminary efficacy and safety, and provide a basis for Phase III trial design and dosing regimen determination.

Timeline

Start
2025-04-03
Primary completion
2026-09-01
Completion
2026-12-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator Escitalopram Small molecule 10 mg Oral
Subject LV232 Unknown 40 mg Oral
Subject LV232 Unknown 60 mg Oral