
District Court Rules Against Teva in Copaxone Patent Lawsuit
Teva said it plans to appeal a district court decision that invalidated several of the company’s Copaxone patents.
Teva suffered a blow on Jan. 30, 2017 after a United States District Court in Delaware invalidated several of the company’s patents for Copaxone (glatiramer acetate injection) 40 mg/mL, the company’s blockbuster multiple sclerosis treatment. In
, Teva alleged infringement on four Copaxone method-of-use patents ’250, ‘413, ‘776, and ‘302 by five of six abbreviated new drug application (ANDA) filers.
The district court decision opens Copaxone 40 mg/mL up to generic competition. In a 2017
Heather Bresch, CEO of Mylan, one of the defendants in the suit, called the decision a “positive step” in Mylan’s efforts to bring generic versions of Copaxone to market. In a
An appeal on the horizon?
Teva has already said that it has
Raffat pointed to inconsistencies between testimony and Teva’s Gala protocol, saying this supports the idea that the company was aware of the rush to patent a “more tolerable” version of the drug. He continued, “The court sees the '250, '413, '302, and '776 patents as nothing more than ‘life-cycle management’-an attempt to continue to monopolize a multi-billion dollar market for a blockbuster drug.” Bloomberg
Source: Teva, Mylan, US District Court of Delaware, Evercore ISI
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