Elotuzumab
Monoclonal antibody | |
---|---|
Type | Whole antibody |
Source | Humanized |
Target | SLAMF7 (CD319) |
Clinical data | |
Trade names | Empliciti |
Pregnancy category |
|
Routes of administration | IV |
Legal status |
|
Pharmacokinetic data | |
Bioavailability | 100% (IV) |
Identifiers | |
CAS Number | 915296-00-3 |
ATC code | None |
IUPHAR/BPS | 8361 |
DrugBank | DB06317 |
ChemSpider | none |
UNII | 1351PE5UGS |
Chemical data | |
Formula | C6476H9982N1714O2016S42 |
Molar mass | 145.5 kg/mol |
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Elotuzumab (brand name Empliciti, previously known as HuLuc63) is a humanized monoclonal antibody used in relapsed multiple myeloma.[1] The package insert denotes its mechanism as a SLAMF7-directed (also known as CD 319) immunostimulatory antibody.[2]
Approvals and indications
In May 2014, it was granted "Breakthrough Therapy" designation by the FDA. [3] On November 30, 2015, FDA approved elotuzumab as a treatment for patients with multiple myeloma who have received one to three prior medications.[1] Elotuzumab was labeled for use with lenalidomide and dexamethasone. Each intravenous injection of elotuzumab should be premedicated with dexamethasone, diphenhydramine, ranitidine and acetaminophen.[2]
References
- 1 2 "Press Announcement—FDA approves Empliciti, a new immune-stimulating therapy to treat multiple myeloma". U.S. Food and Drug Administration. Retrieved 3 December 2015.
- 1 2 "Empliciti (elotuzumab) for Injection, for Intravenous Use. Full Prescribing Information" (PDF). Empliciti (elotuzumab) for US Healthcare Professionals. Bristol-Myers Squibb Company, Princeton, NJ 08543 USA.
- ↑ "Bristol-Myers Squibb and AbbVie Receive U.S. FDA Breakthrough Therapy Designation for Elotuzumab, an Investigational Humanized Monoclonal Antibody for Multiple Myeloma" (Press release). Princeton, NJ & North Chicago, IL: Bristol-Myers Squibb. 2014-05-19. Retrieved 2015-02-05.
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