Mar 29 2012
Aperion Biologics, Inc. announced that it has completed patient enrollment and implantation in the Company's clinical trial of its Z-Lig™ Anterior Cruciate Ligament Reconstruction (ACLR) Device for the treatment of ligament injuries of the knee. The prospective, randomized and blinded multicenter study commenced in January 2011 in both Europe and South Africa to provide safety and performance data in the reconstruction of patients' knees with primary ACL ruptures. The goal of the 60-patient study is to establish non-inferiority of the Z-Lig to allograft and the results will be used to support regulatory commercialization approvals and subsequent clinical acceptance of the Z-Lig ACLR device in select markets outside of the United States.
"The availability of high quality allograft tissue is an issue in Italy and in many parts of the world so having an option like the Z-Lig is potentially very beneficial for patients and surgeons," said Stefano Zaffagnini, M.D., Department of Sports Traumatology and Biomechanics Lab, Rizzoli Orthopaedic Institute in Bologna, Italy.
Dr. Willem van der Merwe of the Sports Science Orthopaedic Clinic in Cape Town, South Africa said, "With enrollment complete, our initial impressions are quite favorable with respect to clinical utility. The focus is now on continuing to observe performance as more patients return to activity. Having the Z-Lig as a biologic graft option for ligament reconstruction is an exciting development on the horizon."
"Completion of enrollment in the Z-Lig ACLR multi-national clinical trial is a milestone and we continue to be encouraged by the progress of patients with respect to safety and performance," said Daniel R. Lee, Aperion Biologics' CEO.
The ACL is the most commonly injured knee ligament. Over 800,000 knee ligament reconstruction surgeries are estimated to be performed each year worldwide.
The Z-Lig is currently available only for clinical investigation purposes at this time.
SOURCE Aperion Biologics, Inc.