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Zydus Cadila division settles patent litigation with Adamas Pharma over dyskinesia drug Gocovri

Farhat NasimWritten by Farhat Nasim Published On 2021-02-17T18:23:14+05:30  |  Updated On 17 Feb 2021 6:23 PM IST
Zydus Cadila division settles patent litigation with Adamas Pharma over dyskinesia drug Gocovri
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New Delhi: The US generic drug division of Zydus Cadila Healthcare, Zydus Pharmaceuticals (USA) Inc., and Zydus Worldwide DMCC recently entered into a settlement agreement with Adamas Pharmaceuticals, Inc for resolving the ongoing litigation concerning Zydus's Abbreviated New Drug Application ("ANDA") seeking approval by the U.S. Food and Drug Administration to market a generic version of GOCOVRI (amantadine) extended-release capsules.

An announcement in this regard was recently made by Adamas Pharma.

Under the settlement agreement, Adamas grants Zydus a non-exclusive license to make, use, sell, offer to sell, and import generic versions of GOCOVRI as of March 4, 2030, or earlier in certain circumstances, including the potential for an accelerated license date if the unit sales of GOCOVRI in the 12-month period ending July 31, 2025, or any subsequent 12-month period decline by a specified percentage below the unit sales of GOCOVRI in the year ended December 31, 2019.

GOCOVRI (amantadine) extended-release capsules is the first and only FDA-approved medicine indicated for the treatment of dyskinesia in patients with Parkinson's disease receiving levodopa-based therapy, with or without concomitant dopaminergic medications. It is also the only medicine clinically proven to reduce both dyskinesia and OFF.

"I am pleased to announce the swift settlement of this litigation which reaffirms the strength of our intellectual property and gives us confidence in the opportunity to deliver GOCOVRI to the patients who may benefit for years to come," said Neil F. McFarlane, Chief Executive Officer.

"We are focused on building on the momentum from our strong 2020 performance and delivering growth for GOCOVRI in 2021, " he added.

In accordance with the settlement agreement, the parties will submit a joint stipulation and order to the United States District Court for the District of New Jersey, and the settlement agreement to the U.S. Federal Trade Commission and the U.S. Department of Justice. Upon entry of the joint stipulation and order, this settlement agreement will conclude all patent litigation brought to date by Adamas against generic pharmaceutical companies that filed an ANDA seeking approval to market generic versions of GOCOVRI prior to the expiration of the patents listed in the Orange Book.

zydus cadilazydus pharmaAdamas Pharmapatentpatent litigationdyskinesiaparkinsons diseaseGocovrizydusamantadineusfda
Farhat Nasim
Farhat Nasim

    Farhat Nasim joined Medical Dialogue an Editor for the Business Section in 2017. She Covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a graduate of St.Xavier’s College Ranchi. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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