drugset / Trial / NCT07494305

Multicenter Study to Assess the Efficacy and Safety of LB-102 in the Treatment of Adult Patients With BP1MDE.

NCT07494305 ↗

Phase 2 Recruiting 320 enrolled LB Pharmaceuticals Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Phase II study for patients with Bipolar 1 Disorder experiencing major depressive episode. Patient eligible for enrollment will be randomized (like flipping a coin) to either active drug (LB-102 or placebo). Treatment is for 6 weeks.

Timeline

Start
2026-01-23
Primary completion
2028-02
Completion
2028-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator LB-102 Small molecule 50 mg Oral

Indications