drugset / Trial / NCT00350415

A Double Blind Study for the Treatment of Acute Ulcerative Colitis

NCT00350415

Phase 3 Completed 772 enrolled Warner Chilcott
RandomizedParallel-groupDouble-blindTreatment

Summary

A Double-blind, Randomized, 6-week, Parallel-group Design Clinical trial to assess the Safety and Efficacy of Asacol 4.8 g/day (800 mg mesalamine tablet) versus Asacol 2.4 g/day (400 mg mesalamine tablet) for the Treatment of Moderately Active Ulcerative Colitis (ASCEND III).

Timeline

Start
2006-06
Primary completion
2007-05
Completion
2007-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Mesalamine Small molecule 400 mg Oral
Subject Mesalamine Small molecule 800 mg Oral

Indications