drugset / Trial / NCT06024642

Study of V117957 in Overactive Bladder Syndrome

NCT06024642

Phase 1 Completed 51 enrolled Imbrium Therapeutics Purdue Pharma LP · collab
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability and efficacy of V117957 in subjects with overactive bladder syndrome, compared to placebo.

Timeline

Start
2022-06-30
Primary completion
2024-05-21
Completion
2024-05-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Sunobinop Small molecule 1 mg Oral

Indications