Overview
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 Per
Status:
Completed
Completed
Trial end date:
2014-09-01
2014-09-01
Target enrollment:
Participant gender: