COHERUS BIOSCIENCES

COHERUS BIOSCIENCES

approved_indications FDA Approved Biologics and Pending Applications

Cimerli

ranibizumab-eqrn
aBL 761165

Loqtorzi

toripalimab-tpzi
BL 761240

Udenyca®

pegfilgrastim-cbqv
aBL 761039

Yusimry

adalimumab-aqvh
aBL 761216

approved_indications Inter Partes Review Proceedings

ENBRELIPR2017-01916
IPR2017-02066
HUMIRA / YUSIMRYIPR2016-00172
IPR2016-00188
IPR2016-00189
IPR2016-01018
IPR2017-00822
IPR2017-00823
IPR2017-00826 / IPR2017-01008
IPR2017-00827 / IPR2017-01009
YUSIMRY / IDACIOPGR2019-00064

approved_indications U.S. Patent Litigations

AMJEVITA / YUSIMRY1:19-cv-00139 (D. Del.)
NEULASTA / UDENYCA1:17-cv-00546 (D. Del.)
56-2017-00493553-CU-BT-VTA (CA Sup. Ct.)

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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