Clinical Trials · NCT02590432
An Open-Label, Long-term Study to Assess the Immunogenicity of LINZESS® (Linaclotide) Administered Orally to Adult Participants With Irritable Bowel Syndrome With Constipation or Chronic Idiopathic Constipation
- Phase
- Phase 4
- Recruitment status
- Completed
- Sponsor
- Forest Laboratories
- Enrollment
- 828
- Start date
- Nov 2015
- Locations
- 79 sites, United States
- Primary endpoint
- Number of Participants With Positive Treatment-Related Anti-Drug Antibodies (ADA) in Serum