JANSSEN (CENTOCOR)

JANSSEN (CENTOCOR)

approved_indications FDA Approved Biologics and Pending Applications


Carvykti®

ciltacabtagene autoleucel
BL 125746

Darzalex Faspro®

daratumumab; hyaluronidase-fihj
BL 761145

Darzalex®

daratumumab
BL 761036

Remicade®

infliximab
BL 103772

ReoPro®

abciximab
BL 103575

Rybrevant

amivantamab-vmjw
BL 761210

Simponi Aria®

golimumab
BL 125433

Simponi®

golimumab
BL 125289

Stelara®

ustekinumab
BL 125261 [BL 761044]

Sylvant®

siltuximab
BL 125496

Talvey

talquetamab-tgvs
BL 761342

Tecvayli

teclistamab-cqyv
BL 761291

Tremfya®

guselkumab
BL 761061

approved_indications Inter Partes Review Proceedings


CARVYKTIIPR2021-01484
EPOGEN / PROCRIT / RETACRITIPR2013-00365
EYLEA / M710IPR2022-01225
IPR2022-01226
IPR2023-00099
IPR2024-00201
IPR2024-00298
STELARA / BMAB 1200IPR2023-01444
STELARA / SB17IPR2023-01103

approved_indications U.S. Patent Litigations


DARZALEX1:16-cv-00221 (D. Del.)
HUMIRA2:07-cv-00139 (E.D. Tex.)
2:09-cv-00389 (E.D. Tex.)
REMICADE1:14-cv-07049 (S.D.N.Y.)
1:14-cv-11613 (D. Mass.)
1:15-cv-10698 (D. Mass.)
1:16-cv-00071 (N.D. Utah)
1:16-cv-11117 (D. Mass.)
1:17-cv-11008 (D. Mass.)
2:17-cv-03524 (D.N.J.)
SIMPONI4:09-cv-11362 (D. Mass.)
4:09-cv-40089 (D. Mass.)
STELARA1:22-cv-01549 (D. Del.)
4:09-cv-11340 (D. Mass.)
REMICADE / INFLECTRA1:14-cv-07049 (S.D.N.Y.)
1:14-cv-11613 (D. Mass.)
1:15-cv-10698 (D. Mass.)
1:16-cv-11117 (D. Mass.)
1:17-cv-11008 (D. Mass.)
REMICADE / RENFLEXIS2:17-cv-03524 (D.N.J.)
REOPRO / GENENTECH CABILLY2:08-cv-03573 (C.D. Cal.)
STELARA / WEZLANA1:22-cv-01549 (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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