Clinical Trials Directory

Trials / Terminated

TerminatedNCT02120027

52-Week Efficacy and Safety Study of Ibodutant in Women With Irritable Bowel Syndrome With Diarrhea (IBS-D)

A 52-Week, Double-blind, Randomised, Placebo-controlled, Parallel-group Phase III Study With Re-randomisations at Week 25 to Evaluate the Efficacy and Safety of Oral Ibodutant 10 mg Once Daily in Female Patients With Irritable Bowel Syndrome With Diarrhoea (IBS-D)

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
558 (actual)
Sponsor
Menarini Group · Industry
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Irritable Bowel Syndrome with diarrhoea (IBS-D) is a functional gastrointestinal disorder characterised by chronic or recurrent abdominal pain or discomfort and diarrhoea. This trial aims at the evaluation of the efficacy and safety of oral ibodutant 10 mg once daily as compared to placebo in women with IBS-D over a 24-week treatment period.

Detailed description

The study evaluates the efficacy and safety of ibodutant 10 mg, given once daily for 24 weeks in comparison with placebo in female IBS-D patients. Randomisation to ibodutant and placebo will be 1:1. Efficacy is evaluated in terms of weekly response for abdominal pain intensity and stool consistency over 24 weeks of treatment in at least 50% of the weeks of treatment. The clinical phase of the study comprises up to 2 weeks of screening for patient's eligibility, a 2-week run-in period (treatment-free) for IBS severity assessment, a first 24-week double-blind treatment period, a second 28-week re-randomised double-blind treatment period and a 2-week safety follow-up, resulting in a maximum 58-week overall duration of the study for each patient. Patients report their IBS-related symptoms daily in a telephone-based electronic diary from run-in until end of treatment.

Conditions

Interventions

TypeNameDescription
DRUGIbodutant 10 mgOral tablet, to be given once daily.
DRUGPlaceboOral tablet (identical in appearance and weight to ibodutant tablets) to be given once daily.

Timeline

Start date
2014-02-01
Primary completion
2015-11-01
Completion
2015-11-01
First posted
2014-04-22
Last updated
2017-03-03
Results posted
2017-01-18

Locations

139 sites across 9 countries: United States, Czechia, Germany, Hungary, Latvia, Poland, Slovakia, Sweden, United Kingdom

Source: ClinicalTrials.gov record NCT02120027. Inclusion in this directory is not an endorsement.