drugset / Trial / NCT06828887
Dose-Finding Clinical Trial to Evaluate the Efficacy and Safety of LV232 Capsules in the Treatment of MDD
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Escitalopram | Small molecule | 10 mg | Oral |
| Subject | LV232 | Unknown | 40 mg | Oral |
| Subject | LV232 | Unknown | 60 mg | Oral |