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Vilobelimab

ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Also known as: CaCP29, gohibic, IFX-1

EMA approvedATC L04AJ10

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

Key facts

Vilobelimab is a drug catalogued in DrugCentral. It was first approved by the EMA in 2025. DrugCentral lists 1 molecular target, including C5. Recorded indications include SARS-CoV2-induced acute respiratory distress syndrom.

  • Molecular targets: C5 (1 listed in DrugCentral).
  • Indications: SARS-CoV2-induced acute respiratory distress syndrom.
  • ATC code: L04AJ10 (Complement inhibitors).

Indications & contraindications

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

Indications (1)

  • SARS-CoV2-induced acute respiratory distress syndrom

Mechanism & targets

Molecular targets (1)

TargetGeneActionActivity
Complement C5C5otherKd 9.59

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2025-01-13EMA—InflaRx GmbH

ATC classification

ATC codeTherapeutic hierarchy
L04AJ10ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSUPPRESSANTS › IMMUNOSUPPRESSANTS › Complement inhibitors

Chemical structure

Molecular formula—
Molecular weight—
CAS number—
InChIKey—
PubChem CID137254326

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Vilobelimab used for?

DrugCentral lists the following indications for Vilobelimab: SARS-CoV2-induced acute respiratory distress syndrom.

How does Vilobelimab work?

Its molecular targets in DrugCentral include C5.

When was Vilobelimab first approved?

Vilobelimab was first approved by the EMA in 2025.

Browse: all drugs starting with V · 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 approval2025-01-13
AgencyEMA
Targets1
Indications1
Formula—
DrugCentral ID5761
Interactive profile