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

CompletedPhase 4Linaclotide (Approved)
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
View Linaclotide compound reference