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Drug

Vilobelimab

Approved medicine
ClassComplement C5 inhibitorResearchOngoing clinical research

Also known as Gohibic, INV-VILOBELIMAB.

Complement C5
Primary target
1
Regulatory events

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Vilobelimab
Aliases & brands
GohibicINV-VILOBELIMAB
RxNorm CUI
2639620
ChEMBL ID
CHEMBL2109636
ATC codes
L04AJ10
UNII
F5T0RF9ZJA
Primary mechanism
Complement C5 inhibitor
Regulatory jurisdictions
ema

Pharmacology & targets

1 target

Known molecular targets and mechanisms supported by curated pharmacology databases.

Complement C5
C5 · P01031
INHIBITORComplement C5 inhibitor

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
2025-01-13
Latest approval
2025-01-13
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2025-01-13Approval
Approval: Gohibic (EMA)
Indication: Gohibic is indicated for the treatment of adult patients with SARS-CoV2-induced acute respiratory distress syndrome (ARDS) who are receiving systemic corticosteroids as part ofShow full indication

Gohibic is indicated for the treatment of adult patients with SARS-CoV2-induced acute respiratory distress syndrome (ARDS) who are receiving systemic corticosteroids as part of Standard of Care and receiving invasive mechanical ventilation (IMV) (with or without extracorporeal membrane oxygenation (ECMO)).

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

3 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
3
registered trials across all phases
LATEST COMPLETION 2022
1
Late-stage (III+)
1
Completed
2
Discontinued
PHASE DISTRIBUTIONn = 3
Phase 22Phase 31

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.