Clinical Trials · NCT00306748

Phase 2 Study of MD-1100 Acetate Administered for 14 Days to Patients Meeting Criteria for Chronic Constipation

CompletedPhase 2Linaclotide (Approved)
Phase
Phase 2
Recruitment status
Completed
Sponsor
Ironwood Pharmaceuticals, Inc.
Enrollment
40
Start date
Mar 2006
Locations
14 sites, United States
Primary endpoint
Safety will be evaluated on an ongoing basis by completing physical examinations, ECGs, clinical laboratory tests, and adverse event reporting.
View Linaclotide compound reference