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Anakinra

Interleukin-1 Receptor Antagonist — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Also known as: kineret

EMA approvedFDA approvedATC L04AC03

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

Key facts

Anakinra is a drug in the Interleukin-1 Receptor Antagonist class catalogued in DrugCentral. It was first approved by the FDA in 2001. Its mechanism of action is classified as Interleukin 1 Receptor Antagonists. DrugCentral lists 1 molecular target, including IL1R1|IL1RAP. Recorded indications include Chronic infantile neurological, cutaneous and articular syndrome, COVID19 pneumonia requiring supplemental oxygen, Cryopyrin associated periodic syndrome and Familial Mediterranean fever.

  • Drug class: Interleukin-1 Receptor Antagonist.
  • Mechanism of action: Interleukin 1 Receptor Antagonists.
  • Molecular targets: IL1R1|IL1RAP (1 listed in DrugCentral).
  • Indications: Chronic infantile neurological, cutaneous and articular syndrome, COVID19 pneumonia requiring supplemental oxygen, Cryopyrin associated periodic syndrome, Familial Mediterranean fever and Rheumatoid arthritis and others.
  • ATC code: L04AC03 (Interleukin inhibitors).
  • Molecular formula: C759H1186N208O232S10; molecular weight 17257.66 g/mol.

Indications & contraindications

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

Indications (6)

  • Chronic infantile neurological, cutaneous and articular syndrome
  • COVID19 pneumonia requiring supplemental oxygen
  • Cryopyrin associated periodic syndrome
  • Familial Mediterranean fever
  • Rheumatoid arthritis
  • Still's disease

Mechanism & targets

Mechanism of action (MoA)Interleukin 1 Receptor Antagonists
Established pharmacologic classInterleukin-1 Receptor Antagonist

Molecular targets (1)

TargetGeneActionActivity
Interleukin-1 receptor, type IIL1R1|IL1RAPantagonistKd 7.82

Regulatory approvals (2)

DateAgencyMarketed asApplicantOrphan
2002-03-08EMA——
2001-11-14FDA—BIOVITRUM AB

ATC classification

ATC codeTherapeutic hierarchy
L04AC03ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSUPPRESSANTS › IMMUNOSUPPRESSANTS › Interleukin inhibitors

Pharmacogenomics

Drug-label and guideline annotations from PharmGKB and CPIC.

  • EMA label: NLRP3
  • FDA label: IL1RN
  • FDA label: NLRP3
  • HCSC label: NLRP3

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
Drug ineffective1325.3
Off label use1195.0
Haemophagocytic lymphohistiocytosis1048.9
Apparent death966.5
Polyarthritis833.8
Red blood cell sedimentation rate abnormal826.7
Adrenal insufficiency621.8
Joint destruction588.2
Human antichimeric antibody positive584.3
Body height below normal580.7
Bone density decreased515.7
Red blood cell sedimentation rate increased509.6

Chemical structure

Molecular formulaC759H1186N208O232S10
Molecular weight17257.66 g/mol
CAS number143090-92-0
InChIKey—
PubChem CID—

Frequently asked questions

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

What is Anakinra used for?

DrugCentral lists the following indications for Anakinra: Chronic infantile neurological, cutaneous and articular syndrome, COVID19 pneumonia requiring supplemental oxygen, Cryopyrin associated periodic syndrome, Familial Mediterranean fever, Rheumatoid arthritis and Still's disease.

How does Anakinra work?

Anakinra is classified as Interleukin 1 Receptor Antagonists; its molecular targets in DrugCentral include IL1R1|IL1RAP (antagonist).

When was Anakinra first approved?

Anakinra was first approved by the FDA in 2001.

What drug class does Anakinra belong to?

Anakinra is in the Interleukin-1 Receptor Antagonist class.

What is the chemical formula of Anakinra?

Anakinra has the molecular formula C759H1186N208O232S10 and a molecular weight of 17257.66 g/mol.

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 approval2001-11-14
AgencyFDA
Targets1
Indications6
FormulaC759H1186N208O232S10
DrugCentral ID5017
Interactive profile