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AboutPricing
Drug ReportsElotuzumab
Empliciti(elotuzumab)
Empliciti (elotuzumab) is an antibody pharmaceutical. Elotuzumab was first approved as Empliciti on 2015-11-30. It is used to treat multiple myeloma in the USA. It has been approved in Europe to treat multiple myeloma. The pharmaceutical is active against SLAM family member 7.
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Case Study: Multiple Myeloma
Events Timeline
Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
cardiovascular diseasesD002318
hemic and lymphatic diseasesD006425
immune system diseasesD007154
Trade Name
FDA
EMA
Empliciti
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Elotuzumab
Tradename
Proper name
Company
Number
Date
Products
EmplicitielotuzumabBristol Myers SquibbN-761035 RX2015-11-30
2 products
Labels
FDA
EMA
Brand Name
Status
Last Update
emplicitiBiologic Licensing Application2022-03-22
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
multiple myeloma—D009101C90.0
Agency Specific
FDA
EMA
Expiration
Code
elotuzumab, Empliciti, Bristol-Myers Squibb Company
2025-11-06Orphan excl.
Patent Expiration
No data
ATC Codes
L: Antineoplastic and immunomodulating agents
— L01: Antineoplastic agents
— L01F: Monoclonal antibodies and antibody drug conjugates
— L01FX: Other monoclonal antibodies and antibody drug conjugates in atc
— L01FX08: Elotuzumab
HCPCS
Code
Description
J9176
Injection, elotuzumab, 1 mg
Clinical
Clinical Trials
71 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple myelomaD009101—C90.0173614—768
Plasma cell neoplasmsD054219——173414—766
LymphomaD008223—C85.91—1——2
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Smoldering multiple myelomaD000075122———2———2
Plasma cell leukemiaD007952—C90.1—1———1
Essential thrombocythemiaD013920—D47.3—1———1
Polycythemia veraD011087—D45—1———1
Primary myelofibrosisD055728—D47.4—1———1
ThrombocytosisD013922HP_0001894D75.83—1———1
PolycythemiaD011086EFO_0005804D75.1—1———1
RecurrenceD012008———1———1
Immunoglobulin light-chain amyloidosisD000075363———1———1
AmyloidosisD000686EFO_1001875E85—1———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
LeukemiaD007938—C951————1
Myeloid leukemia acuteD015470—C92.01————1
Myeloid leukemiaD007951—C921————1
Non-hodgkin lymphomaD008228—C85.91————1
Follicular lymphomaD008224—C821————1
Mantle-cell lymphomaD020522——1————1
Waldenstrom macroglobulinemiaD008258HP_0005508C88.01————1
Large b-cell lymphoma diffuseD016403—C83.31————1
B-cell lymphomaD016393——1————1
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameElotuzumab
INNelotuzumab
Description
Elotuzumab (humanized mab)
Classification
Antibody
Drug classmonoclonal antibodies
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Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL1743010
ChEBI ID—
PubChem CID—
DrugBankDB06317
UNII ID1351PE5UGS (ChemIDplus, GSRS)
Target
Agency Approved
SLAMF7
SLAMF7
Organism
Homo sapiens
Gene name
SLAMF7
Gene synonyms
CS1
NCBI Gene ID
Protein name
SLAM family member 7
Protein synonyms
19A24 protein, CD2 subset 1, CD2-like receptor activating cytotoxic cells, CD2-like receptor-activating cytotoxic cells, CD319, CRACC, Membrane protein FOAP-12, Novel Ly9, novel LY9 (lymphocyte antigen 9) like protein, Protein 19A
Uniprot ID
Mouse ortholog
Slamf7 (75345)
SLAM family member 7 (Q8BHK6)
Alternate
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Empliciti – Bristol Myers Squibb
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Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 2,251 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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3,378 adverse events reported
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