Empliciti® (elotuzumab)

BL 761035

Empliciti® (elotuzumab)

BL 761035

U.S. License Holder:

Bristol-Myers Squibb

Date of License:

November-30-2015

Last Update:

Dec-15-2024

approved_indications FDA-Approved Indications

EMPLICITI (elotuzumab) is a SLAMF7-directed immunostimulatory antibody indicated in:

Combination with lenalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one to three prior therapies;

Combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least two prior therapies including lenalidomide and a proteasome inhibitor.

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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