drugset / Trial / NCT00295854

Phase II Study Efficacy and Safety of Two Dosing Regimens of MN-001 in Patients With Interstitial Cystitis

NCT00295854 ↗

Phase 2 Completed 296 enrolled MediciNova
RandomizedParallel-groupTriple-blindTreatment

Summary

To evaluate the safety and efficacy of 8 weeks of treatment with MN-001 at 500 mg bid, 500 mg once daily vs. placebo in patients with Interstitial Cystitis.

Timeline

Start
2005-05
Primary completion
2006-10
Completion
2006-10

Drugs

EvaluationDrugModalityDoseRoute
Subject tipelukast Small molecule 500 mg —

Indications