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Drug

Ranibizumab

Established medicine
ResearchActive indication expansion
Also known as Byooviz, Cimerli, Lucentis, RBZ+2 more

Byooviz, Cimerli, Lucentis, RBZ, Susvimo, rhuFab V2.

RxNorm595060UNIIZL1R02VT79
1
Research papers
20
Regulatory events
Latest activity
beta

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

Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy.

Research2017-07-25De Cillà S · Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Profile

Identifiers & mechanism

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

Canonical name
Ranibizumab
Aliases & brands
ByoovizCimerliLucentisRBZSusvimorhuFab V2
RxNorm CUI
595060
UNII
ZL1R02VT79
Regulatory jurisdictions
emafda

Regulatory timeline

20 events

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.

Approval / market entry confirmed across FDA and EMA (2026-05-04 → 2026-09-18)
Generic / biosimilar approval confirmed across FDA and EMA (2021-08-18 → 2022-11-09)
Earliest approval
2007-01-22
Latest approval
2026-09-18
Authorities
FDA · EMA
Total events
20
fdaU.S. Food and Drug Administration· 10 events
2026-09-01Label change
Label change: RANIBIZUMAB-NUNA (BLA761202)
Evidence ↗
2026-05-04Supplemental approvalMulti-authority
Supplemental approval: RANIBIZUMAB-NUNA (BLA761202)
Evidence ↗
2026-03-30Label change
Label change: RANIBIZUMAB-NUNA (BLA761202)
Evidence ↗
emaEuropean Medicines Agency· 10 events
2026-10-16CHMP positive opinion
CHMP positive opinion: Fovlussea (EMA)

Indication: Treatment of neovascular (wet) age-related macular degeneration (AMD), and other visual impairments in adults

Evidence ↗
2026-09-18Original application approvalMulti-authority
Marketing authorisation: Susvimo (EMA)
Indication: Susvimo is indicated in adult patients for the treatment of neovascular (wet) age-related macular degeneration (nAMD) who have achieved stable disease after previously responding… Show full indication

Susvimo is indicated in adult patients for the treatment of neovascular (wet) age-related macular degeneration (nAMD) who have achieved stable disease after previously responding to intravitreal treatment with a vascular endothelial growth factor (VEGF) inhibitor medicinal product.

Evidence ↗
2026-07-24CHMP positive opinion
CHMP positive opinion: Susvimo (EMA)

Indication: Treatment of adults with neovascular (wet) age-related macular degeneration (AMD).

Evidence ↗

Data from the U.S. Food and Drug Administration (U.S. Food and Drug Administration), public domain (CC0).

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

Research activity

1 paper

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

Most influential

Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2017 · 16 cites
Recent papers

Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2017 · 16 cites
Journals, researchers & institutions
Top journals
  • Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology1
Leading researchers
  • Casini G1
  • Clemente N1
  • De Cillà S1
  • Farruggio S1
  • Filippini D1
  • Gatti V1
  • Grossini E1
  • Mary D1
Leading institutions
free-text, unnormalised
  • Eye Clinic1
  • University East Piedmont1
  • University of Pisa1

Related drugs

5 matches

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

Frequently co-studied with Ranibizumab in the research literature.

1 shared paper

Frequently co-studied with Ranibizumab in the research literature.

1 shared paper

Frequently co-studied with Ranibizumab in the research literature.

1 shared paper

Frequently co-studied with Ranibizumab in the research literature.

1 shared paper

Frequently co-studied with Ranibizumab in the research literature.

1 shared paper
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • Europe PMC — research literature
  • Regulatory event sources are credited in the Regulatory Timeline above.