Elotuzumab

Elotuzumab (brand name Empliciti, (Bristol-Myers Squibb and AbbVie), 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]

Elotuzumab
Monoclonal antibody
TypeWhole antibody
SourceHumanized
TargetSLAMF7 (CD319)
Clinical data
Trade namesEmpliciti
License data
Pregnancy
category
  • US: X (Contraindicated)
Routes of
administration		IV
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability100% (IV)
Identifiers
CAS Number
IUPHAR/BPS
DrugBank
ChemSpider
  • none
UNII
KEGG
Chemical and physical data
FormulaC6476H9982N1714O2016S42
Molar mass145453.59 g·mol−1
 NY (what is this?)  (verify)

Approvals and indications

Multiple myeloma

In May 2014, it was granted "Breakthrough Therapy" designation by the FDA (for multiple myeloma).[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] In May 2016 the EC/EU gave a similar approval.[4]

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gollark: *M L I s s I m I l a r*
gollark: ML-syntax Rust ≈good.
gollark: ++exec```haskellimport Data.Monoidimport Control.Applicativeimport Data.Listimport Control.Monadit = join.liftA2(<>)inits tailsallCombs xs = [1..] >>= \n -> mapM (const xs) [1..n]main = putStr . concat . take 1000 . nub . allCombs $ "gollark"```

References
  1. "Press Announcement—FDA approves Empliciti, a new immune-stimulating therapy to treat multiple myeloma". U.S. Food and Drug Administration. Retrieved 3 December 2015.
  2. "Empliciti (elotuzumab) for Injection, for Intravenous Use. Full Prescribing Information" (PDF). Empliciti (elotuzumab) for US Healthcare Professionals. Princeton, New Jersey: Bristol-Myers Squibb Company. Archived from the original (PDF) on 2015-12-08.
  3. "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, New Jersey and North Chicago, Illinois: Bristol-Myers Squibb. 2014-05-19. Retrieved 2015-02-05.
  4. BMS gets two new cancer approvals in Europe. May 2016
  • "Elotuzumab". Drug Information Portal. U.S. National Library of Medicine.


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