drugset / Trial / NCT01233960

Evaluation of PROCHYMAL® for Treatment-refractory Moderate-to-severe Crohn's Disease

NCT01233960

Phase 3 Completed 73 enrolled Mesoblast, Inc.
NaSingle-groupOpen-labelTreatment

Summary

To provide open-label re-treatment with PROCHYMAL to participants enrolled in companion Protocol 603 to evaluate the safety in participants with active Crohn's disease who are resistant to standard Crohn's disease therapies.

Timeline

Start
2010-11-29
Primary completion
2014-09-15
Completion
2014-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Prochymal® Cell therapy 200 cells Intravenous

Indications