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
| Type | Name | Description |
|---|---|---|
| DRUG | Ibodutant 10 mg | Oral tablet, to be given once daily. |
| DRUG | Placebo | Oral 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.