drugset / Trial / NCT01041001

Study to Compare Efficacy and Safety of Cartistem and Microfracture in Patients With Knee Articular Cartilage Injury

NCT01041001 ↗

Phase 3 Completed 104 enrolled Medipost Co Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to assess and compare the safety and efficacy of the allogeneic-unrelated umbilical cord blood-derived mesenchymal stem cell product (Cartistem®) to that of a microfracture treatment in patients with articular cartilage defect or injury.

Timeline

Start
2009-02
Primary completion
2010-12
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject CARTISTEM Cell therapy 500 unknown Other