Clinical Trials · NCT02559817

A Safety and Efficacy Study of a Range of Linaclotide Doses Administered Orally to Children Ages 7-17 Years, With Irritable Bowel Syndrome With Constipation

TerminatedPhase 2Linaclotide (Prohibited)
Phase
Phase 2
Recruitment status
Terminated
Sponsor
Forest Laboratories
Enrollment
101
Start date
Nov 2015
Locations
48 sites, United States, Canada
Primary endpoint
Change From Baseline in 4-week Overall Spontaneous Bowel Movement (SBM) Frequency Rate (SBMs/Week) During the Treatment Period
View Linaclotide compound reference