Trial Details

COMPLETED
Basic Information
Clinical ID c3052
Identifier NCT02590432
Trial Title 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
Trial URL Visit Original Page
Study Information
Study Results

YES

Conditions Irritable Bowel Syndrome With Constipation|Chronic Idiopathic Constipation
Interventions DRUG: Linaclotide
Participant Information
Sponsor Forest Laboratories
City Anniston
Country/Region United States
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type INTERVENTIONAL
Phase PHASE4
Time Information
Start Date 2015-11-01
Primary Completion Date 2018-02-05
Completion Date 2018-02-05