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Drug ReportsRanibizumab
Lucentis(ranibizumab)
Byooviz, Cimerli, Lucentis, Ranivisio, Susvimo, Ximluci (ranibizumab) is an antibody pharmaceutical. Ranibizumab was first approved as Lucentis on 2006-06-30. It is used to treat diabetic retinopathy, macular edema, and retinal vein occlusion in the USA. It has been approved in Europe to treat choroidal neovascularization, degenerative myopia, diabetes complications, diabetic retinopathy, and macular edema amongst others. The pharmaceutical is active against vascular endothelial growth factor A, long form. In addition, it is known to target Vascular permeability factor.
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Events Timeline
Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
eye diseasesD005128
cardiovascular diseasesD002318
endocrine system diseasesD004700
Trade Name
FDA
EMA
Byooviz, Cimerli, Lucentis, Susvimo
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Ranibizumab
Tradename
Proper name
Company
Number
Date
Products
LucentisranibizumabGenentechN-125156 RX2006-06-30
4 products
SusvimoranibizumabGenentechN-761197 RX2021-10-22
1 products
Labels
FDA
EMA
Brand Name
Status
Last Update
byoovizBiologic Licensing Application2025-01-15
cimerliBiologic Licensing Application2024-06-17
lucentisBiologic Licensing Application2024-11-18
susvimoBiologic Licensing Application2024-11-22
Agency Specific
FDA
EMA
Expiration
Code
ranibizumab, Cimerli, Coherus BioSciences, Inc.
10/3/2023Interchangeable excl.
Patent Expiration
No data
ATC Codes
S: Sensory organ drugs
— S01: Ophthalmologicals
— S01L: Ocular vascular disorder agents
— S01LA: Antineovascularisation agents
— S01LA04: Ranibizumab
HCPCS
Code
Description
J2778
Injection, ranibizumab, 0.1 mg
Clinical
Clinical Trials
628 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Macular degenerationD008268EFO_0001365H35.30161023846
Macular edemaD008269———41613538
EdemaD004487HP_0000969R60.9—41410331
Choroidal neovascularizationD020256——15116324
Pathologic neovascularizationD009389——15116223
Retinal vein occlusionD012170EFO_1001157H34.81——95317
Vision disordersD014786HP_0000505H53.11—1113217
Low visionD015354———1113116
Retinal diseasesD012164HP_0000479H35.9—23329
Diabetic retinopathyD003930EFO_0003770——116—8
Show 11 more
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Premature birthD047928EFO_0003917O60——2—24
Retinopathy of prematurityD012178EFO_1001158H35.1——2—24
MyopiaD009216EFO_0003927H52.1—13——4
GlaucomaD005901EFO_0000516H40—12—13
Neovascular glaucomaD015355EFO_1001060———2——2
Diabetes mellitusD003920HP_0000819E08-E13——2——2
Degenerative myopiaD047728—H44.2—11——2
HemorrhageD006470MP_0001914R58—11——1
Diabetes complicationsD048909———11——1
Vitreous hemorrhageD014823EFO_0008626H43.1—11——1
Show 2 more
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
UveitisD014605HP_0000554H20.9—1———1
Central serous chorioretinopathyD056833—H35.7111———1
Pseudoxanthoma elasticumD011561Orphanet_758Q82.8—1———1
Retinal telangiectasisD058456Orphanet_190H35.02—1———1
TelangiectasisD013684———1———1
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
IschemiaD007511EFO_0000556—————11
PapilledemaD010211EFO_1001074H35.81————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameRanibizumab
INNranibizumab
Description
Immunoglobulin G1, anti-(human vascular endothelial growth factor) Fab fragment (human-mouse monoclonal rhuFAB V2 gamma1-chain), disulfide with human-mouse monoclonal rhuFAB V2 kappa-chain
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
>1CZ8:H,Y|HEAVY CHAIN OF NEUTRALIZING ANTIBODY EVQLVESGGGLVQPGGSLRLSCAASGYDFTHYGMNWVRQAPGKGLEWVGWINTYTGEPTYAADFKRRFTFSLDTSKSTAY LQMNSLRAEDTAVYYCAKYPYYYGTSHWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPV TVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHL >1CZ8:L,X|LIGHT CHAIN OF NEUTRALIZING ANTIBODY DIQLTQSPSSLSASVGDRVTITCSASQDISNYLNWYQQKPGKAPKVLIYFTSSLHSGVPSRFSGSGSGTDFTLTISSLQP EDFATYYCQQYSTVPWTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQ ESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Identifiers
PDB1CZ8
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL1201825
ChEBI ID—
PubChem CID—
DrugBankDB01270
UNII IDZL1R02VT79 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
VEGFA
VEGFA
Organism
Homo sapiens
Gene name
VEGFA
Gene synonyms
NCBI Gene ID
—
Protein name
Vascular endothelial growth factor A
Protein synonyms
Vascular permeability factor
Uniprot ID
Mouse ortholog
—
—
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Cimerli – Coherus BioSciences
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Byooviz – Biogen
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Lucentis – Novartis
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Lucentis – Roche
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Tabular view
Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 13,769 documents
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Safety
Black-box Warning
Black-box warning for: Susvimo
Adverse Events
Top Adverse Reactions
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29,511 adverse events reported
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