In a filing to the BSE, Natco said the US Supreme Court remanded the case relating to Teva's 'patent no 5,800,808' back to US Court of Appeals for the Federal Circuit for that court "to review the patent's validity in accordance with a partially modified standard of review".
Natco had entered into an exclusive licensing and supply agreement with Mylan Laboratories for glatiramer acetate, the generic version of Teva's Copaxone in June 2008. It had, however, faced patent litigation from Teva.
This was, however, reversed by the Federal Circuit Court ruling in 2013 stating the patent was invalid and it was challenged by Teva in the US Supreme Court.
"The Supreme Court made no finding as to the validity of the US'808 patent, but instead sent the case back to the Federal Court to consider the matter in view of the modified standard," Natco Pharma said in its filing.
Although the current case relates to strength of 20mg/ml, Natco had last year announced that its marketing partner Mylan had filed an Abbreviated New Drug Application (ANDA) for generic Copaxone of 40mg/ml strength and expected 180 days of marketing exclusivity.
On the other hand commenting on the development, Teva President and CEO said: "We are encouraged by the U S Supreme Court's Decision and look forward to the Federal Circuit's review.
"We will continue to explore all available avenues to protect our intellectual property for Copaxone 20mg/mL."
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