Clinical Trials · NCT00460811

Randomized, Double-blind, Dose-range-finding, Phase 2 Study of Linaclotide Administered to Patients With Irritable Bowel Syndrome With Constipation (IBS-C)

CompletedPhase 2Linaclotide (Approved)
Phase
Phase 2
Recruitment status
Completed
Sponsor
Ironwood Pharmaceuticals, Inc.
Enrollment
420
Start date
Apr 2007
Locations
85 sites, United States, Canada
Primary endpoint
Change From Baseline in the Weekly Normalized Complete Spontaneous Bowel Movement (CSBM) Rate During Weeks 1 Through 12 of the Treatment Period
View Linaclotide compound reference