NCT01656720
A Multi-centre, Phase II, Double-blind, Randomised, Placebo-controlled, Parallel Group, Dose-ranging Study in Patients With Faecal Incontinence; to Evaluate the Efficacy, Safety and Tolerability of Locally Applied NRL001 Over an 8 Week Treatment Period
Phase: Phase 2
Role: Lead Sponsor
Start: Feb 29, 2012
Completion: Sep 30, 2014