Trial Details

TERMINATED
Basic Information
Clinical ID c1733
Identifier NCT01349673
Trial Title The Safety and Tolerability of Budesonide Foam in Participants With Active Ulcerative Proctitis or Proctosigmoiditis
Trial URL Visit Original Page
Study Information
Study Results

YES
Conditions Proctitis|Proctosigmoiditis
Interventions DRUG: Budesonide Foam
Participant Information
Sponsor Bausch Health Americas, Inc.
City Houston
Country/Region United States
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type INTERVENTIONAL
Phase PHASE3
Time Information
Start Date 2011-05-31
Primary Completion Date 2014-12-31
Completion Date 2014-12-31