Brodalumab
Interleukin-17 Receptor A Antagonist — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: AMG 827, AMG-827, kyntheum
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Brodalumab is a drug in the Interleukin-17 Receptor A Antagonist class catalogued in DrugCentral. It was first approved by the PMDA in 2016. Its mechanism of action is classified as Interleukin 17 Receptor A Antagonists. DrugCentral lists 1 molecular target, including IL17RA|IL17RC. Recorded indications include Ankylosing spondylitis, Erythrodermic psoriasis, Non-radiographic axial spondyloarthritis and Palmoplantar pustulosis.
- Drug class: Interleukin-17 Receptor A Antagonist.
- Mechanism of action: Interleukin 17 Receptor A Antagonists.
- Molecular targets: IL17RA|IL17RC (1 listed in DrugCentral).
- Indications: Ankylosing spondylitis, Erythrodermic psoriasis, Non-radiographic axial spondyloarthritis, Palmoplantar pustulosis and Plaque psoriasis and others.
- ATC code: L04AC12 (Interleukin inhibitors).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (7)
- Ankylosing spondylitis
- Erythrodermic psoriasis
- Non-radiographic axial spondyloarthritis
- Palmoplantar pustulosis
- Plaque psoriasis
- Psoriatic arthritis
- Pustular psoriasis
Contraindications (1)
- Crohn's disease
Mechanism & targets
| Mechanism of action (MoA) | Interleukin 17 Receptor A Antagonists |
|---|---|
| Established pharmacologic class | Interleukin-17 Receptor A Antagonist |
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Interleukin-17 receptor | IL17RA|IL17RC | other | Kd 9.20 |
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2017-07-17 | EMA | — | LEO Pharma A/S | |
| 2017-02-15 | FDA | — | VALEANT LUXEMBOURG | |
| 2016-07-04 | PMDA | — | — |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L04AC12 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSUPPRESSANTS › IMMUNOSUPPRESSANTS › Interleukin inhibitors |
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 |
|---|---|
| Psoriatic arthropathy | 133.6 |
| Psoriasis | 117.5 |
| Patient dissatisfaction with treatment | 69.0 |
| Therapy interrupted | 67.7 |
| Suicidal ideation | 63.1 |
| Drug ineffective | 62.4 |
| Parakeratosis | 60.1 |
| Collagen-vascular disease | 56.8 |
| Tinea pedis | 55.4 |
| Dermatitis infected | 53.3 |
| Disease recurrence | 50.1 |
| Arthralgia | 49.6 |
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 Brodalumab used for?
DrugCentral lists the following indications for Brodalumab: Ankylosing spondylitis, Erythrodermic psoriasis, Non-radiographic axial spondyloarthritis, Palmoplantar pustulosis, Plaque psoriasis, Psoriatic arthritis and Pustular psoriasis.
How does Brodalumab work?
Brodalumab is classified as Interleukin 17 Receptor A Antagonists; its molecular targets in DrugCentral include IL17RA|IL17RC.
When was Brodalumab first approved?
Brodalumab was first approved by the PMDA in 2016.
What drug class does Brodalumab belong to?
Brodalumab is in the Interleukin-17 Receptor A Antagonist class.
Browse: all drugs starting with B · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5179 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1742996 — compound record and bioactivity
- DrugBank DB11776 — drug record
- FDA UNII 6ZA31Y954Z — substance identity
- DailyMed: FDA labels for Brodalumab — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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.