Elranatamab
ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: elranatamab-bcmm, elrexfio, PF-06863135, RN613
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Elranatamab is a drug catalogued in DrugCentral. It was first approved by the FDA in 2023. DrugCentral lists 2 molecular targets, including TNFRSF17 and CD3E. Recorded indications include Relapsed or refractory multiple myeloma.
- Molecular targets: TNFRSF17 and CD3E (2 listed in DrugCentral).
- Indications: Relapsed or refractory multiple myeloma.
- ATC code: L01FX32 (Other monoclonal antibodies and antibody drug conjugates).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Relapsed or refractory multiple myeloma
Mechanism & targets
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Tumor necrosis factor receptor superfamily member 17 | TNFRSF17 | other | Kd 10.42 |
| T-cell surface glycoprotein CD3 epsilon chain | CD3E | other | Kd 7.77 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2023-08-14 | FDA | — | PFIZER INC | Yes |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L01FX32 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES › Other monoclonal antibodies and antibody drug conjugates |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label
- FDA label
- HCSC label
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Cytokine release syndrome | 1369.0 |
| Immune effector cell-associated neurotoxicity syndrome | 478.9 |
| Cytomegalovirus infection reactivation | 312.8 |
| Cytomegalovirus infection | 164.2 |
| Hypogammaglobulinaemia | 132.7 |
| Malignant neoplasm progression | 128.1 |
| Death | 97.2 |
| Neoplasm progression | 97.1 |
| Neutropenia | 75.6 |
| Pyrexia | 72.7 |
| Second primary malignancy | 64.4 |
| Progressive multifocal leukoencephalopathy | 63.4 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 2408850-14-4 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Elranatamab used for?
DrugCentral lists the following indications for Elranatamab: Relapsed or refractory multiple myeloma.
How does Elranatamab work?
Its molecular targets in DrugCentral include TNFRSF17 and CD3E.
When was Elranatamab first approved?
Elranatamab was first approved by the FDA in 2023.
Browse: all drugs starting with E · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5741 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL4297809 — compound record and bioactivity
- DrugBank DB15395 — drug record
- FDA UNII L0HR9A577V — substance identity
- DailyMed: FDA labels for Elranatamab — current prescribing information (label search)
- UniProt Q02223 (TNFRSF17) — target protein
- UniProt P07766 (CD3E) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
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