drugset / Trial / NCT00679380

(CB-01-02/02) Randomized Placebo Controlled Trial of Budesonide-multi-matrix System (MMX™) 6 mg and 9 mg in Patients With Ulcerative Colitis

NCT00679380 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This will be a multicentre, randomised, double-blind, double-dummy, parallel group comparative study in patients with mild or moderate, active ulcerative colitis. The study will compare budesonide-MMX™ 6 mg and budesonide-MMX™ 9 mg tablets to placebo and to Entocort® 3 x 3 mg capsules, in four parallel groups of patients over an 8 week treatment period. After the screening visit, patients will enter a washout period of 2 days, then they will be randomised to the following four treatment groups: budesonide-MMX™ tablets (6 mg), budesonide-MMX™ tablets (9 mg), Entocort® capsules (3 x 3 mg) and placebo (tablets and capsules), all administered once a day after breakfast. Hence, each patient will receive, in the morning after breakfast, either one budesonide-MMX™ 6 mg or budesonide MMX™ 9 mg tablet and 3 placebo Entocort® matching capsules, or three Entocort® 3 mg capsules and one placebo budesonide-MMX™ matching tablet, or one placebo budesonide-MMX™ matching tablet and three placebo Entocort® matching capsules.

Timeline

Start
2008-06
Primary completion
2010-02
Completion
2010-04

Outcome

Met primary endpoint

registry analysis (unspecified test); 2: Budesonide-MMX® 9 mg vs 4: Placebo; p = 0.0047; Difference in proportions 12.9 (95% CI 4.6 to 21.3); Chi-squared NCT00679380 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Budesonide Small molecule 6 mg Oral
Subject Budesonide Small molecule 9 mg Oral

Indications