drugset / Trial / NCT01059344

Efficacy and Safety of Asacol™ 4.8 g/Day (800 mg Tablets) for the Treatment of Active Ulcerative Colitis

NCT01059344

Phase 3 Completed 281 enrolled Tillotts Pharma AG
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to determine the efficacy of Asacol™ 4.8 g/day (800 mg tablets) to induce clinical and endoscopic remission after 6 weeks of treatment compared to placebo in subjects with active ulcerative colitis (UC).

Timeline

Start
2009-11
Primary completion
2011-07
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Mesalamine Small molecule 4.8 g

Indications