BRISTOL-MYERS SQUIBB

ERBITUXIPR2016-00458
OPDIVOIPR2016-01217
IPR2016-01218
IPR2016-01219
IPR2016-01221
IPR2023-00249
IPR2023-00252
IPR2023-00501
IPR2025-00601
IPR2025-00602
IPR2025-00603
ORENCIAIPR2015-01537
OPDIVO / KEYTRUDAIPR2016-01217
IPR2016-01218
IPR2016-01219
IPR2016-01221
OPDIVO / YERVOYIPR2025-00601
IPR2025-00602
IPR2025-00603

U.S. Patent Litigations

ERBITUX2:13-cv-05400 (N.D. Cal.)
2:15-cv-06133 (E.D. Pa.)
3:13-cv-02045 (N.D. Cal.)
ERBITUX / GENENTECH CABILLY / YERVOY2:13-cv-05400 (N.D. Cal.)
3:13-cv-02045 (N.D. Cal.)
OPDIVO / BAVENCIO1:17-cv-01029 (D. Del.)
OPDIVO / IMFINZI1:17-cv-01028 (D. Del.)
1:22-cv-00346 (D. Del.)
1:23-cv-00459 (D. Del.)
OPDIVO / KEYTRUDA1:14-cv-01131 (D. Del.)
1:15-cv-00560 (D. Del.)
1:15-cv-00572 (D. Del.)
OPDIVO / TECENTRIQ1:17-cv-01027 (D. Del.)
YERVOY / IMJUDO1:23-cv-00079 (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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BRISTOL-MYERS SQUIBB

FDA Approved Biologics and Pending Applications

Inter Partes Review Proceedings

U.S. Patent Litigations

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