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
- 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