Daclizumab
Interleukin-2 Receptor Blocking Antibody — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: zenapax, zinbryta
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Daclizumab is a drug in the Interleukin-2 Receptor Blocking Antibody class catalogued in DrugCentral. It was first approved by the FDA in 1997. Its mechanism of action is classified as Interleukin 2 Receptor Antagonists and Interleukin 2 Receptor-directed Antibody Interactions. DrugCentral lists 1 molecular target, including IL2RA|IL2RB|IL2RG. Recorded indications include Relapsing remitting multiple sclerosis and Renal transplant rejection.
- Drug class: Interleukin-2 Receptor Blocking Antibody.
- Mechanism of action: Interleukin 2 Receptor Antagonists; Interleukin 2 Receptor-directed Antibody Interactions.
- Molecular targets: IL2RA|IL2RB|IL2RG (1 listed in DrugCentral).
- Indications: Relapsing remitting multiple sclerosis and Renal transplant rejection.
- ATC code: L04AC01 (Interleukin inhibitors).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (2)
- Relapsing remitting multiple sclerosis
- Renal transplant rejection
Mechanism & targets
| Mechanism of action (MoA) | Interleukin 2 Receptor Antagonists; Interleukin 2 Receptor-directed Antibody Interactions |
|---|---|
| Established pharmacologic class | Interleukin-2 Receptor Blocking Antibody |
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Interleukin-2 receptor | IL2RA|IL2RB|IL2RG | other | Kd 8.00 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1999-02-26 | EMA | — | — | |
| 1997-12-10 | FDA | — | HOFFMAN-LA ROCHE |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L04AC01 | 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 |
|---|---|
| Transplant dysfunction | 2444.6 |
| Ovarian cyst | 1892.3 |
| Transplant rejection | 1784.1 |
| Acne | 1562.3 |
| Alopecia | 791.6 |
| Multiple sclerosis relapse | 471.8 |
| Liver function test abnormal | 426.4 |
| Sleep disorder due to general medical condition, insomnia type | 308.5 |
| Rheumatoid arthritis | 185.7 |
| Kidney transplant rejection | 132.6 |
| Pneumonia | 127.2 |
| Loss of personal independence in daily activities | 100.0 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 152923-56-3 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Daclizumab used for?
DrugCentral lists the following indications for Daclizumab: Relapsing remitting multiple sclerosis and Renal transplant rejection.
How does Daclizumab work?
Daclizumab is classified as Interleukin 2 Receptor Antagonists and Interleukin 2 Receptor-directed Antibody Interactions; its molecular targets in DrugCentral include IL2RA|IL2RB|IL2RG.
When was Daclizumab first approved?
Daclizumab was first approved by the FDA in 1997.
What drug class does Daclizumab belong to?
Daclizumab is in the Interleukin-2 Receptor Blocking Antibody class.
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Sources
- DrugCentral drug card 4953 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1201605 — compound record and bioactivity
- DrugBank DB00111 — drug record
- FDA UNII CUJ2MVI71Y — substance identity
- DailyMed: FDA labels for Daclizumab — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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