Epcoritamab
Bispecific CD20-directed CD3 T Cell Engager — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: epcoritamab-bysp, epkinly, GEN3013
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Epcoritamab is a drug in the Bispecific CD20-directed CD3 T Cell Engager class catalogued in DrugCentral. It was first approved by the FDA in 2023. Its mechanism of action is classified as CD20-directed Antibody Interactions, CD3 Receptor Agonists and CD3-directed Antibody Interactions. DrugCentral lists 2 molecular targets, including CD3E|CD3G|CD3D and MS4A1. Recorded indications include Relapsed or refractory diffuse large B-cell lymphoma.
- Drug class: Bispecific CD20-directed CD3 T Cell Engager.
- Mechanism of action: CD20-directed Antibody Interactions; CD3 Receptor Agonists; CD3-directed Antibody Interactions.
- Molecular targets: CD3E|CD3G|CD3D and MS4A1 (2 listed in DrugCentral).
- Indications: Relapsed or refractory diffuse large B-cell lymphoma.
- ATC code: L01FX27 (Other monoclonal antibodies and antibody drug conjugates).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Relapsed or refractory diffuse large B-cell lymphoma
Mechanism & targets
| Mechanism of action (MoA) | CD20-directed Antibody Interactions; CD3 Receptor Agonists; CD3-directed Antibody Interactions; Cytochrome P450 Inhibitors |
|---|---|
| Established pharmacologic class | Bispecific CD20-directed CD3 T Cell Engager |
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| T-cell surface glycoprotein CD3 | CD3E|CD3G|CD3D | other | EC50 8.80 |
| B-lymphocyte antigen CD20 | MS4A1 | other | EC50 8.61 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2023-09-22 | EMA | — | AbbVie Deutschland GmbH & Co. KG | |
| 2023-05-19 | FDA | — | GENMAB US, INC. |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L01FX27 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES › Other monoclonal antibodies and antibody drug conjugates |
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 | 4532.2 |
| Immune effector cell-associated neurotoxicity syndrome | 790.8 |
| Febrile neutropenia | 378.0 |
| Pyrexia | 319.4 |
| COVID-19 | 250.5 |
| Cytomegalovirus infection reactivation | 171.4 |
| Sepsis | 135.6 |
| COVID-19 pneumonia | 129.0 |
| Hypogammaglobulinaemia | 121.6 |
| Tumour pseudoprogression | 116.2 |
| Cytomegalovirus infection | 114.7 |
| Diffuse large B-cell lymphoma | 114.0 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | — |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Epcoritamab used for?
DrugCentral lists the following indications for Epcoritamab: Relapsed or refractory diffuse large B-cell lymphoma.
How does Epcoritamab work?
Epcoritamab is classified as CD20-directed Antibody Interactions, CD3 Receptor Agonists and CD3-directed Antibody Interactions; its molecular targets in DrugCentral include CD3E|CD3G|CD3D and MS4A1.
When was Epcoritamab first approved?
Epcoritamab was first approved by the FDA in 2023.
What drug class does Epcoritamab belong to?
Epcoritamab is in the Bispecific CD20-directed CD3 T Cell Engager class.
Browse: all drugs starting with E · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5734 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL4650393 — compound record and bioactivity
- DrugBank DB16672 — drug record
- FDA UNII D6OMY2L0WA — substance identity
- DailyMed: FDA labels for Epcoritamab — current prescribing information (label search)
- UniProt P11836 (MS4A1) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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