Back to discover
Drug

Faricimab

Approved · EMA
ClassVascular endothelial growth factor A inhibitorEmerging researchLate-stage development

Also known as Vabysmo.

3
Research papers
17
Active clinical trials
2
Protein targets
1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Approval: Vabysmo (EMA)

Regulatory2022-09-15EMA

Profile

Identifiers & mechanism

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

Canonical name
Faricimab
Aliases & brands
Vabysmo
RxNorm CUI
2591519
ChEMBL ID
CHEMBL4297750
ATC codes
S01LA09
UNII
QC4F7FKK7I
Primary mechanism
Vascular endothelial growth factor A inhibitor
Regulatory jurisdictions
ema

Pharmacology & targets

2 targets

Known molecular targets and mechanisms supported by curated pharmacology databases.

INHIBITORVascular endothelial growth factor A inhibitor
Angiopoietin-2
ANGPT2 · O15123
INHIBITORAngiopoietin-2 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
2022-09-15
Latest approval
2022-09-15
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2022-09-15Approval
Approval: Vabysmo (EMA)
Indication: Vabysmo is indicated for the treatment of adult patients with: neovascular (wet) age-related macular degeneration (nAMD), visual impairment due to diabetic macular oedema (DME),Show full indication

Vabysmo is indicated for the treatment of adult patients with: neovascular (wet) age-related macular degeneration (nAMD), visual impairment due to diabetic macular oedema (DME), visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO).

Evidence ↗

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

Clinical trials

36 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
36
registered trials across all phases
LATEST COMPLETION 2026
17
Active studies
13
Recruiting
25
Late-stage (III+)
18
Completed
1
Discontinued
PHASE DISTRIBUTIONn = 36
Phase 12Phase 1 / 21Phase 28Phase 2 / 31Phase 312Phase 49Phase N / A3

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.

Research activity

3 papers

Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.

Publications over time
20222026
Major research themes7
Angiogenesis Inhibitors2Angiopoietin-22Antibodies, Bispecific1Diabetic Retinopathy1Macular Degeneration1Macular Edema1Vascular Endothelial Growth Factor A1
Journals, researchers & institutions
Top journals
  • Lancet (London, England)1
  • Ophthalmology1
  • Ophthalmology science1
Leading researchers
  • Gibson K2
  • Khanani AM2
  • Kotak A2
  • Lai TYY2
  • Sheth VS2
  • Abreu F1
  • Amador M1
  • Basu K1
Leading institutions
free-text, unnormalised
  • The Chinese University of Hong Kong2
  • Center of Ophthalmology1
  • Clinica Baviera1
  • Clinica de Ojos Garza Viejo1
  • Department of Ophthalmology and GRADE Reading Center1
  • Eye Clinic1

Related drugs

1 matches

Drugs sharing diseases, protein targets and literature with this one. Ranked by graph evidence (shared targets + diseases weighted above co-mentions).

Acts on the same molecular target as Faricimab, with an overlapping disease area.

Shared target1 shared disease1 shared paper
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • Europe PMC — research literature
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.