FORMYCON

FDA Approved Biologics and Pending Applications

Ahzantive®

aflibercept-mrbb
aBL 761378

Nufymco

ranibizumab-leyk
aBL 761473

Otulfi®

ustekinumab-aauz
aBL 761379

Approved Foreign Follow-On Biologics / Biosimilars

Biosimilars Approved In The E.U.

Ahzantive® / Baiama® (aflibercept) (Formycon / Klinge Biopharma) (January-2025)Fymskina (Formycon) (ustekinumab) (September-2024)

Inter Partes Review Proceedings

EYLEA / AHZANTIVEIPR2025-00233

U.S. Patent Litigations

EYLEA / AHZANTIVE1:23-cv-00097 (N.D.W. Va.) / MDL 1:24-md-03103 (N.D.W. Va.)

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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