drugset / Trial / NCT01433432

Open Label Extension Study to Protocol C2/13/DR-6MP-02

NCT01433432 ↗

Phase 2 Withdrawn Teva GTC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The open label extension study (Protocol C2/13/DR-6MP-02 EXT) is designed to evaluate the clinical efficacy and safety of 80 mg DR-6MP test formulation for an additional 12 weeks in subjects who already completed 12 weeks of Protocol C2/13/DR-6MP-02. Crohn's disease (CD) therapy is aimed at reducing inflammation via induction of remission after a flare-up and maintenance of the remission for as long as possible. The questions being asked in this extension study are: 1. For subjects who received 80 mg DR-6MP for 12 weeks: Can the clinical efficacy and safety status achieved following 12 weeks of treatment be maintained or improved following an additional 12 weeks of DR-6MP treatment? 2. For subjects who received oral Purinethol (1-1.5 mg/kg daily) for 12 weeks: Can the clinical efficacy and safety at 12 weeks be maintained or improved following the introduction of 12 weeks of 80 mg DR-6MP treatment?

Timeline

Start
2011-10
Primary completion
2012-06
Completion
2012-08

Outcome

Outcome not reported

Stopped: “Sponsor withdrew support for study due to reorganization and project prioritization”

Drugs

EvaluationDrugModalityDoseRoute
Subject DR-6MP Unknown 80 mg —

Indications