Lanadelumab
Plasma Kallikrein Inhibitor — BLOOD AND BLOOD FORMING ORGANS
Also known as: DX-2930, lanadelumab (genetical recombination), Lanadelumab-fyo, SHP 643, takhzyro
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Lanadelumab is a drug in the Plasma Kallikrein Inhibitor class catalogued in DrugCentral. It was first approved by the FDA in 2018. Its mechanism of action is classified as Kallikrein Inhibitors. DrugCentral lists 1 molecular target, including KLKB1. Recorded indications include Hereditary angioneurotic edema.
- Drug class: Plasma Kallikrein Inhibitor.
- Mechanism of action: Kallikrein Inhibitors.
- Molecular targets: KLKB1 (1 listed in DrugCentral).
- Indications: Hereditary angioneurotic edema.
- ATC code: B06AC05 (Drugs used in hereditary angioedema).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Hereditary angioneurotic edema
Mechanism & targets
| Mechanism of action (MoA) | Kallikrein Inhibitors |
|---|---|
| Established pharmacologic class | Plasma Kallikrein Inhibitor |
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Plasma kallikrein | KLKB1 | other | IC50 10.05 |
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2022-03-28 | PMDA | — | Takeda Pharmaceutical Company Limited | Yes |
| 2018-11-22 | EMA | — | SHIRE PHARMACEUTICALS IRELAND LTD | Yes |
| 2018-08-23 | FDA | — | DYAX CORP | Yes |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
B06AC05 | BLOOD AND BLOOD FORMING ORGANS › OTHER HEMATOLOGICAL AGENTS › OTHER HEMATOLOGICAL AGENTS › Drugs used in hereditary angioedema |
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 |
|---|---|
| Hereditary angioedema | 3588.3 |
| Product dose omission issue | 329.7 |
| Inappropriate schedule of product administration | 224.1 |
| Insurance issue | 216.4 |
| Weight increased | 194.7 |
| Injection site pain | 190.7 |
| Pharyngeal swelling | 158.5 |
| Weight decreased | 151.1 |
| Product availability issue | 138.4 |
| No adverse event | 97.1 |
| Stress | 79.7 |
| COVID-19 | 75.6 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 1426055-14-2 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Lanadelumab used for?
DrugCentral lists the following indications for Lanadelumab: Hereditary angioneurotic edema.
How does Lanadelumab work?
Lanadelumab is classified as Kallikrein Inhibitors; its molecular targets in DrugCentral include KLKB1.
When was Lanadelumab first approved?
Lanadelumab was first approved by the FDA in 2018.
What drug class does Lanadelumab belong to?
Lanadelumab is in the Plasma Kallikrein Inhibitor class.
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Sources
- DrugCentral drug card 5309 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL3545189 — compound record and bioactivity
- DrugBank DB14597 — drug record
- FDA UNII 2372V1TKXK — substance identity
- DailyMed: FDA labels for Lanadelumab — current prescribing information (label search)
- UniProt P03952 (KLKB1) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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