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Lanadelumab

Plasma Kallikrein Inhibitor — BLOOD AND BLOOD FORMING ORGANS

Also known as: DX-2930, lanadelumab (genetical recombination), Lanadelumab-fyo, SHP 643, takhzyro

EMA approvedFDA approvedPMDA approvedOrphan designationATC B06AC05

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 classPlasma Kallikrein Inhibitor

Molecular targets (1)

TargetGeneActionActivity
Plasma kallikreinKLKB1otherIC50 10.05

Regulatory approvals (3)

DateAgencyMarketed asApplicantOrphan
2022-03-28PMDA—Takeda Pharmaceutical Company LimitedYes
2018-11-22EMA—SHIRE PHARMACEUTICALS IRELAND LTDYes
2018-08-23FDA—DYAX CORPYes

ATC classification

ATC codeTherapeutic hierarchy
B06AC05BLOOD 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 termLLR
Hereditary angioedema3588.3
Product dose omission issue329.7
Inappropriate schedule of product administration224.1
Insurance issue216.4
Weight increased194.7
Injection site pain190.7
Pharyngeal swelling158.5
Weight decreased151.1
Product availability issue138.4
No adverse event97.1
Stress79.7
COVID-1975.6

Chemical structure

Molecular formula—
Molecular weight—
CAS number1426055-14-2
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.

Browse: all drugs starting with L · 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 approval2018-08-23
AgencyFDA
Targets1
Indications1
Formula—
DrugCentral ID5309
Interactive profile