Belimumab
B Lymphocyte Stimulator-specific Inhibitor — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: benlysta, LymphoStat B, LymphoStat-B
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Belimumab is a drug in the B Lymphocyte Stimulator-specific Inhibitor class catalogued in DrugCentral. It was first approved by the FDA in 2011. Its mechanism of action is classified as B Lymphocyte Stimulator-directed Antibody Interactions. DrugCentral lists 1 molecular target, including TNFSF13B. Recorded indications include Systemic lupus erythematosus.
- Drug class: B Lymphocyte Stimulator-specific Inhibitor.
- Mechanism of action: B Lymphocyte Stimulator-directed Antibody Interactions.
- Molecular targets: TNFSF13B (1 listed in DrugCentral).
- Indications: Systemic lupus erythematosus.
- ATC code: L04AG04 (Monoclonal antibodies).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Systemic lupus erythematosus
Mechanism & targets
| Mechanism of action (MoA) | B Lymphocyte Stimulator-directed Antibody Interactions |
|---|---|
| Established pharmacologic class | B Lymphocyte Stimulator-specific Inhibitor |
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Tumor necrosis factor ligand superfamily member 13B | TNFSF13B | other | — |
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2017-09-27 | PMDA | — | GlaxoSmithKline KK | |
| 2011-07-13 | EMA | — | Glaxo Group Ltd. | |
| 2011-03-09 | FDA | — | HUMAN GENOME SCIENCES INC. |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L04AG04 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSUPPRESSANTS › IMMUNOSUPPRESSANTS › Monoclonal antibodies |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label: TNFSF13B
- FDA label: TNFSF13B
- HCSC label: TNFSF13B
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 |
|---|---|
| Product dose omission issue | 1460.0 |
| Lupus nephritis | 798.5 |
| Product complaint | 629.6 |
| Wrong technique in device usage process | 461.9 |
| Therapy interrupted | 384.4 |
| SLE arthritis | 301.4 |
| Proteinuria | 220.2 |
| COVID-19 | 216.9 |
| Exposure via skin contact | 207.5 |
| Therapy cessation | 203.1 |
| Product storage error | 182.8 |
| Inappropriate schedule of product administration | 154.8 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 356547-88-1 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Belimumab used for?
DrugCentral lists the following indications for Belimumab: Systemic lupus erythematosus.
How does Belimumab work?
Belimumab is classified as B Lymphocyte Stimulator-directed Antibody Interactions; its molecular targets in DrugCentral include TNFSF13B.
When was Belimumab first approved?
Belimumab was first approved by the FDA in 2011.
What drug class does Belimumab belong to?
Belimumab is in the B Lymphocyte Stimulator-specific Inhibitor class.
Browse: all drugs starting with B · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 4949 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1789843 — compound record and bioactivity
- DrugBank DB08879 — drug record
- FDA UNII 73B0K5S26A — substance identity
- DailyMed: FDA labels for Belimumab — current prescribing information (label search)
- UniProt Q9Y275 (TNFSF13B) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
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