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Nipocalimab

ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Also known as: imaavy, M281, nipocalimab-aahu

EMA approvedFDA approvedPMDA approvedOrphan designationATC L04AL03

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Nipocalimab is a drug catalogued in DrugCentral. It was first approved by the FDA in 2025. DrugCentral lists 1 molecular target, including FCGRT. Recorded indications include Myasthenia gravis.

  • Molecular targets: FCGRT (1 listed in DrugCentral).
  • Indications: Myasthenia gravis.
  • ATC code: L04AL03 (Neonatal fragment crystallizable receptor (FcRn) inhibitors).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (1)

  • Myasthenia gravis

Mechanism & targets

Molecular targets (1)

TargetGeneActionActivity
IgG receptor FcRn large subunit p51FCGRTotherKd 9.68

Regulatory approvals (3)

DateAgencyMarketed asApplicantOrphan
2025-11-28EMA—Janssen Cilag International NVYes
2025-04-29FDA—Johnson & Johnson
2025-04-29PMDA—Janssen Pharmaceutical K.K.

ATC classification

ATC codeTherapeutic hierarchy
L04AL03ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSUPPRESSANTS › IMMUNOSUPPRESSANTS › Neonatal fragment crystallizable receptor (FcRn) inhibitors

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 Nipocalimab used for?

DrugCentral lists the following indications for Nipocalimab: Myasthenia gravis.

How does Nipocalimab work?

Its molecular targets in DrugCentral include FCGRT.

When was Nipocalimab first approved?

Nipocalimab was first approved by the FDA in 2025.

Browse: all drugs starting with N · drug guides by category · protein targets A–Z.

Sources

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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 approval2025-04-29
AgencyFDA
Targets1
Indications1
Formula—
DrugCentral ID5769
Interactive profile