drugset / Trial / NCT01222559

Efficacy and Safety Study of co.Don Chondrosphere to Treat Cartilage Defects

NCT01222559 ↗

Phase 3 Completed 102 enrolled co.don AG
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a prospective, phase III, multicenter, open label, randomised clinical trial of co.don chondrosphere®, a three-dimensional autologous chondrocyte transplantation product (ACT3D-CS)compared to the procedure of microfracture (MF)in the treatment of cartilage defects of knee joints. After screening visit patients were booked for arthroscopy and at that time they were randomised to either ACT3D-CS with co.don chondrosphere® (Group A) or to MF(Group B), a marrow-stimulating method based on the penetration of the subchondral bone plate at the bottom of the cartilage defect. At the time of arthroscopy Patients of group B had their procedure of MF (treatment surgery) and patients of group A had their cells harvested from healthy cartilage. The cells are cultivated for 8-10 weeks in vitro to develope 3-dimensional spheroids , that are transplanted in an open knee procedure (treatment surgery)into the defect. Patients subsequently followed the same rehabilitation program and had post-surgery visits. After the 12-month-visit a interim analyses will be performed and the 24-month-visit is defined as final assessment. Then patients have follow-up assessments up to 60 months post-treatment-surgery.

Timeline

Start
2010-10
Primary completion
2017-09
Completion
2020-02

Outcome

Met primary endpoint

paper According to the between-group analysis, ACI passed the test of noninferiority compared with microfracture; thus, the primary goal of the study was achieved. PMID 31317047 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject co.don chondrosphere® Cell therapy — Other

Indications

No indication recorded.