Sunlight Pharma settles patent dispute for generic lenalidomide capsules in U.S.

Tom Smith

&#13 &#13 Sun Prescription drugs Industries declared that it has arrived at an arrangement with Celgene Corporation (Celgene), a wholly-owned subsidiary of Bristol Myers Squibb, to take care of the patent litigation regarding submission of an Abbreviated New Drug Software (ANDA) for a generic edition of Revlimid (lenalidomide capsules) in […]

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Sun Prescription drugs Industries declared that it has arrived at an arrangement with Celgene Corporation (Celgene), a wholly-owned subsidiary of Bristol Myers Squibb, to take care of the patent litigation regarding submission of an Abbreviated New Drug Software (ANDA) for a generic edition of Revlimid (lenalidomide capsules) in the US.

Pursuant to the terms of the settlement, Celgene will grant Sun Pharma a license to Celgene’s patents required to manufacture and promote (topic to USFDA approval) certain minimal quantity of generic lenalidomide capsules in the US starting on a private day that is someday right after March 2022. In addition, the license will also make it possible for Sunshine Pharma to manufacture and promote an endless amount of generic lenalidomide capsules in the US starting 31 January 2026.

As a consequence of the settlement, all Hatch-Waxman litigation between Sunlight Pharma and Celgene, relating to the Revlimid patents, will be dismissed. &#13
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Additional details pertaining to the settlement are confidential. The agreement is issue to customary regulatory approvals.

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(This story has not been edited by Company Common employees and is vehicle-created from a syndicated feed.)

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