Hyderabad: The United States Court of Appeals for the Federal Circuit has ruled that Dr Reddy’s Laboratories Ltd will infringe on the patent of Sunovion Pharmaceuticals blockbuster drug Lunesta. The court delivered its verdict on Thursday. Setting aside an earlier ruling given by a New Jersey Court, the Federal Circuit Court said that the lower court has ‘erred’ in granting summary judgement of non-infringement by Dr Reddy’s (DRL). Lunesta (eszopiclone) is the prescription brand to treat insomnia. Sunovin is a wholly-owned subsidiary of Dainippon Sumitomo Pharma Co. Ltd (DSP). According to Dainippon Sumitomo Pharma, Lunesta generated USD 136 million revenues in North America and Chinese markets in the April—June quarter of the current fiscal. -"In view of the foregoing, we conclude that the district court’s construction of the asserted claims was correct, but we also conclude that the court erred in granting summary judgement of non-infringement to Reddy. -"Therefore, because Reddy’s ANDA (Abbreviated New Drug Application) specification infringes claim 1 of Sunovion’s ’673 patent as a matter of law, the judgement of the district court is reversed,-" the court said in its order. DRL officials offered no comments on the matter. Commenting on the Lunesta patent case, Sarabjit Kour Nangra (VP-Research, Pharma) Angel Broking said Sunovin has reached settlements with other companies over the sleep medicine, including one with Teva Pharmaceutical Industries Ltd. That enabled low-cost versions to enter the market before the expiry of the patent. -"We maintain our estimates on the company and hence our neutral rating on the stock,” she said. Sunovion, formerly known as Sepracor Inc., filed its infringement suit in March 2009, targeting 10 generics makers including Dr Reddy’s, that had filed ANDAs for their own versions of Lunesta. In January, the New Jersey federal judge observed that Dr Reddy’s didn’t infringe the patent of the drug belonging to Sunovion, and that the Indian drug maker’s proposed generic version of the sleep aid is chemically different. Sunovion argued that the District Court erred in concluding that DRL would not infringe by making and selling its product approved by the FDA.
