ReoPro® (abciximab)

BL 103575

ReoPro® (abciximab)

BL 103575

U.S. License Holder:

Centocor Inc. (Janssen Biotech, Inc.)

Date of License:

December-22-1994

Last Update:

Dec-15-2024

approved_indications FDA-Approved Indications

ReoPro (abciximab) is indicated as an adjunct to percutaneous coronary intervention for the prevention of cardiac ischemic complications:

in patients undergoing percutaneous coronary intervention;

in patients with unstable angina not responding to conventional medical therapy when percutaneous coronary intervention is planned within 24 hours.

approved_indications U.S. Patent Litigations

PACER

Case No(s):

2:08-cv-03573 (C.D. Cal.)

U.S. Patent Nos.
4,816,567 (Recombinant Immunoglobulin Preparations) 6,171,586 (Antibody Formulation) 6,331,415 (Methods of Producing Immunoglobulins, Vectors and Transformed Host Cells for Use Therein) 6,333,398 (Protein Purification) 6,417,335 (Protein Purification) 6,870,034 (Protein Purification)

Plaintiffs
Centocor Ortho Biotech, Inc.

Defendants
City of Hope; Genentech, Inc.

Status
Dismissed

BPCIA
N

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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