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Amgen announced during its Q3 2024 Earnings Call that it had launched Pavblu™ (aflibercept-ayyh) as the first biosimilar of Regeneron’s EYLEA® (aflibercept) to be marketed in the U.S.  The launch follows the Federal Circuit’s decision on October 22, 2024 (CAFC Appeal No. 24-2351) to deny a temporary injunction that would prevent Pavblu™ from launching at-risk while Regeneron appeals an earlier District Court (Case No. 1:24-cv-00039 (N.D.W. Va.) / MDL 1:24-md-03103 (N.D.W. Va.)) denial of a preliminary injunction against Pavblu™ (previously reported Amgen Plans At-Risk Launch of EYLEA® Biosimilar Pavblu™ After Federal Circuit Lifts Temporary Injunction).  The litigation and appeal remain ongoing.

Numerous other EYLEA® biosimilars have had their launches delayed by preliminary injunctions, including Samsung Bioepis’s Opuviz™ (aflibercept-yszy)Formycon’s Ahzantive® (aflibercept-mrbb), and Celltrion’s CT-P42 (aflibercept) (previously reported Preliminary Injunctions Issued Preventing Launch of EYLEA® Biosimilars).  Biocon and Mylan’s Yesafili™ (aflibercept-jbvf) has been permanently enjoined from launching prior to the expiration of Regeneron’s U.S. Patent No. 11,084,865 (previously reported Permanent Injunction Issued Preventing Launch of EYLEA® Biosimilar Yesafili™).

Regeneron reported EYLEA® sales of $5.72 billion in 2023.

There are currently eight ongoing litigations and related appeals for EYLEA® biosimilars.  For more information about these and other biosimilar patent disputes, please visit BiologicsHQ.

 

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The author would like to thank April Breyer Menon for her contributions to this article.


    Methodology

    Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.

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