PALO ALTO, Calif., Jan. 5, 2011 /PRNewswire/ -- Carbylan BioSurgery, Inc. announced today the completion of patient enrollment in their double-blinded, multi-center COR1.0 feasibility trial to evaluate the safety and effectiveness of two products - Hydros and Hydros TA Joint Therapies - in patients with osteoarthritis of the knee. Hydros and Hydros TA are next generation viscosupplement and viscosupplement/steroid combination products.
"Hydros and Hydros TA are designed to offer patients suffering from knee osteoarthritis more effective and safer options for managing the pain associated with their disease, and potentially, may help to delay knee replacement surgery," said George Daniloff, President and CEO of Carbylan BioSurgery. "Carbylan's polymer technology platform uniquely enables products we believe are superior to existing viscosupplement technology."
The COR1.0 clinical trial is being conducted at eight clinical sites in Canada, Belgium, and The Netherlands. The trial is designed to evaluate the safety and efficacy of Hydros and Hydros TA compared with Synvisc-One®, the market leading viscosupplement. A total of 98 patients have been treated in the study and will be followed for six months post injection. Carbylan expects final results from the study in August 2011, with pivotal studies for FDA approval expected to follow.
"We are very pleased that patient enrollment in the COR1.0 study was completed ahead of schedule. We believe this reflects the high level of interest in our product concept from both physicians and patients," commented Marcee Maroney, Vice President of Clinical Affairs and Marketing at Carbylan. "There is a clear clinical need for a safe, fast-acting, long lasting therapy to treat the pain associated with osteoarthritis of the knee. We believe that Hydros and Hydros TA are particularly well positioned to address this need."
In addition, Carbylan announced that