Clinical Trials · NCT01880424

A Phase 3, International, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Efficacy and Safety Trial of Linaclotide Administered Orally for 12 Weeks to Patients With Irritable Bowel Syndrome With Constipation (IBS-C)

CompletedPhase 3Linaclotide (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
AstraZeneca
Enrollment
1,722
Start date
Jul 2013
Locations
82 sites, 5 countries
Primary endpoint
12-week Abdominal Pain/Abdominal Discomfort Weekly Responder
View Linaclotide compound reference