Ibodutant for Relief of Irritable Bowel Syndrome (IRIS)

PHASE2CompletedINTERVENTIONAL
Enrollment

554

Participants

Timeline

Start Date

July 31, 2008

Primary Completion Date

February 28, 2009

Study Completion Date

March 31, 2009

Conditions
Irritable Bowel Syndrome
Interventions
DRUG

Ibodutant

Oral tablet, dose level 1 (10 mg), once daily

DRUG

Ibodutant

Oral tablet, dose level 2 (30 mg), once daily

DRUG

Ibodutant

Oral tablet, dose level 3 (60 mg), once daily

DRUG

Placebo

Oral tablet matching the three dose levels of ibodutant, once daily

Trial Locations (6)

Unknown

Center for Clinical and Basic Research (CCBR), Ballerup Municipality

emovis GmbH, Berlin

"Digestive Diseases Center Gastro", Riga

"Federal State Institution Outpatient clinic #3 of President's Management Department of the Russian Federation", Moscow

Academy of Medical Science of Ukraine, Dnipropetrovsk

Synexus Midlands Clinical Research Centre, Birmingham

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Menarini Group

INDUSTRY

NCT00761007 - Ibodutant for Relief of Irritable Bowel Syndrome (IRIS) | Biotech Hunter | Biotech Hunter