drugset / Trial / NCT01824303

Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Interstitial Cystitis

NCT01824303

Phase 2 Terminated 31 enrolled Allergan TARIS Biomedical, Inc. · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The purposes of the study is to determine if LiRIS®, an investigational drug-delivery system, is safe and tolerable in women with Interstitial Cystitis (IC), and to evaluate any change in IC symptoms following LiRIS administration.

Timeline

Start
2013-03
Primary completion
2014-11
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Lidocaine Other / unclassified 400 mg Other

Indications