Regeneron

Regeneron

EYLEA® (aflibercept) and Soliris® (eculizumab) IPR and BPCIA Litigation Updates
EYLEA® (aflibercept) and Soliris® (eculizumab) IPR and BPCIA Litigation Updates Robert S. Schwartz; Monica Chou; Damineh Morsali, Ph.D. December 31, 2023
EYLEA® (aflibercept) IPR and BPCIA Litigation Updates
EYLEA® (aflibercept) IPR and BPCIA Litigation Updates Damineh Morsali, Ph.D.; Robert S. Schwartz December 15, 2023
BPCIA Litigation Related to Proposed Eylea Biosimilar CT-P42 Filed
BPCIA Litigation Related to Proposed Eylea Biosimilar CT-P42 Filed Damineh Morsali, Ph.D.; Robert S. Schwartz, Ph.D. November 22, 2023
Venable’s BiologicsHQ Monthly Injection – September 2023
Venable’s BiologicsHQ Monthly Injection – September 2023 Damineh Morsali, Ph.D.; Robert S. Schwartz, Ph.D.; Ha Kung Wong October 16, 2023
Venable’s BiologicsHQ Monthly Injection – August 2023
Venable’s BiologicsHQ Monthly Injection – August 2023 Damineh Morsali, Ph.D.; Robert S. Schwartz, Ph.D.; Ha Kung Wong September 12, 2023

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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