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Avelumab

Programmed Death Ligand-1 Blocker — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Also known as: bavencio, MSB0010682, MSB0010718C

EMA approvedFDA approvedPMDA approvedOrphan designationATC L01FF04

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Avelumab is a drug in the Programmed Death Ligand-1 Blocker class catalogued in DrugCentral. It was first approved by the FDA in 2017. Its mechanism of action is classified as Programmed Death Ligand-1 Antagonists and Programmed Death Ligand-1-directed Antibody Interactions. DrugCentral lists 1 molecular target, including CD274. Recorded indications include Maintenance therapy of unresectable urothelial carcinoma in patients who have received chemotherapy, Merkel cell carcinoma and Renal cell carcinoma.

  • Drug class: Programmed Death Ligand-1 Blocker.
  • Mechanism of action: Programmed Death Ligand-1 Antagonists; Programmed Death Ligand-1-directed Antibody Interactions.
  • Molecular targets: CD274 (1 listed in DrugCentral).
  • Indications: Maintenance therapy of unresectable urothelial carcinoma in patients who have received chemotherapy, Merkel cell carcinoma and Renal cell carcinoma.
  • ATC code: L01FF04 (PD-1/PD-L1 (Programmed cell death protein 1/death ligand 1) inhibitors).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (3)

  • Maintenance therapy of unresectable urothelial carcinoma in patients who have received chemotherapy
  • Merkel cell carcinoma
  • Renal cell carcinoma

Mechanism & targets

Mechanism of action (MoA)Programmed Death Ligand-1 Antagonists; Programmed Death Ligand-1-directed Antibody Interactions
Established pharmacologic classProgrammed Death Ligand-1 Blocker

Molecular targets (1)

TargetGeneActionActivity
Programmed cell death 1 ligand 1CD274other—

Regulatory approvals (3)

DateAgencyMarketed asApplicantOrphan
2017-09-27PMDA—Merck Serono Co., Ltd.Yes
2017-09-18EMA—Merck Europe B.V.Yes
2017-03-23FDA—EMD SERONO INC

ATC classification

ATC codeTherapeutic hierarchy
L01FF04ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES › PD-1/PD-L1 (Programmed cell death protein 1/death ligand 1) inhibitors

Pharmacogenomics

Drug-label and guideline annotations from PharmGKB and CPIC.

  • EMA label: CD274
  • FDA label: CD274
  • HCSC label: CD274

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 termLLR
Disease progression726.1
Death289.9
Neoplasm progression283.2
Myocarditis161.3
Hypothyroidism159.1
Interstitial lung disease152.4
Adrenal insufficiency125.7
Pneumonitis117.5
Infusion related reaction109.8
Skin toxicity109.1
Myositis105.0
Chills99.5

Chemical structure

Molecular formula—
Molecular weight—
CAS number1537032-82-8
InChIKey—
PubChem CID—

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Avelumab used for?

DrugCentral lists the following indications for Avelumab: Maintenance therapy of unresectable urothelial carcinoma in patients who have received chemotherapy, Merkel cell carcinoma and Renal cell carcinoma.

How does Avelumab work?

Avelumab is classified as Programmed Death Ligand-1 Antagonists and Programmed Death Ligand-1-directed Antibody Interactions; its molecular targets in DrugCentral include CD274.

When was Avelumab first approved?

Avelumab was first approved by the FDA in 2017.

What drug class does Avelumab belong to?

Avelumab is in the Programmed Death Ligand-1 Blocker class.

Browse: all drugs starting with A · drug guides by category · protein targets A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2017-03-23
AgencyFDA
Targets1
Indications3
Formula—
DrugCentral ID5221
Interactive profile