SANDOZ

SKYRIZIPGR2022-00037
HUMIRA / HYRIMOZIPR2017-01823
IPR2017-01824
IPR2017-01987
IPR2017-01988
IPR2017-02105
IPR2017-02106
IPR2018-00002
IPR2018-00156
RITUXAN / RIXATHONIPR2017-02036
IPR2017-02042
TYSABRI / TYRUKOPGR2022-00054

U.S. Patent Litigations

ENBREL / ERELZI2:16-cv-01118 (D.N.J.)
3:13-cv-02904 (N.D. Cal.)
ENBREL / ETICOVO2:19-cv-11755 (D.N.J.)
EYLEA / ENZEEVU1:24-cv-00085 (N.D.W. Va.) (transferred from 2:24-cv-08760 (D.N.J.)) / MDL 1:24-md-03103 (N.D.W. Va.)
HUMIRA / HYRIMOZ3:18-cv-12668 (D.N.J.)
NEULASTA / ZIEXTENZO2:16-cv-01276 (D.N.J.)
3:16-cv-02581 (N.D. Cal.)
3:19-cv-00977 (N.D. Cal.)
NEUPOGEN / ZARXIO3:14-cv-04741 (N.D. Cal.)
3:19-cv-00977 (N.D. Cal.)
NEUPOGEN / ZARXIO / NEULASTA / ZIEXTENZO3:19-cv-00977 (N.D. Cal.)
PROLIA / XGEVA / JUBBONTI / WYOST1:23-cv-02406 (D.N.J.)
RITUXAN / RIXATHON / GENENTECH CABILLY1:17-cv-13507 (D.N.J.)
TYSABRI / TYRUKO1:22-cv-01190 (D. Del.)

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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