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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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Clinical
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Target
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Financial
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Safety
Events Timeline
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3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
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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 Application2023-10-06
cimerliBiologic Licensing Application2024-06-01
lucentisBiologic Licensing Application2024-02-22
susvimoBiologic Licensing Application2022-11-17
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
626 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_0001365H35.304192704959280
Macular edemaD008269——2354414641188
EdemaD004487HP_0000969R60.91850343326145
Pathologic neovascularizationD009389——193017121077
Retinal vein occlusionD012170EFO_1001157H34.81111319191975
Choroidal neovascularizationD020256——132819121074
Retinal diseasesD012164HP_0000479H35.99211991870
Wet macular degenerationD057135EFO_0004683—72021151167
Diabetic retinopathyD003930EFO_0003770—62114121259
Vascular diseasesD014652EFO_0004264I776716620
Show 34 more
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Retinal degenerationD012162HP_0001105—232——6
UveitisD014605HP_0000554H20.9231——5
PterygiumD011625—H11.0311——4
Degenerative myopiaD047728—H44.2221——4
Diabetes complicationsD048909———11—12
Retinal hemorrhageD012166HP_0000573H35.6111——2
ScotomaD012607HP_0000603H53.12111——2
Diffuse cerebral sclerosis of schilderD002549Orphanet_726G31.81—11——1
Retinal vasculitisD031300EFO_1001156H35.06—11——1
AggressionD000374EFO_0003015———1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
TelangiectasisD013684——73———9
InflammationD007249MP_0001845—12——24
Von hippel-lindau diseaseD006623—Q85.8332———3
Retinal telangiectasisD058456Orphanet_190H35.0212——13
Angioid streaksD000793EFO_1000805—11——12
SyndromeD013577——21———2
Central serous chorioretinopathyD056833—H35.7121———2
Pseudoxanthoma elasticumD011561Orphanet_758Q82.812———2
HistoplasmosisD006660EFO_0007310B3912———2
Choroidal effusionsD000080324—H31.4—1———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
PainD010146EFO_0003843R521———12
Corneal neovascularizationD016510EFO_1000880H16.42————2
Hereditary hemorrhagic telangiectasiaD013683—I78.01————1
EpistaxisD004844EFO_0003895R04.01————1
Pathologic processesD010335——1————1
DepressionD003863—F33.91————1
Port-wine stainD019339—Q82.51————1
Capillary hemangiomaD018324—Q82.51————1
Neurofibromatosis 1D009456—Q85.011————1
NeurofibromatosesD017253—Q85.001————1
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Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
ChorioretinitisD002825HP_0012424H30————11
Refractive errorsD012030EFO_0003908H52.7————11
Intraocular pressureD007429——————11
Regional blood flowD012039——————11
Cataract extractionD002387——————11
Premature infant diseasesD007235——————11
Laser coagulationD017075——————11
Intravitreal injectionsD058449——————11
Researcher-subject relationsD035844——————11
Epiretinal membraneD019773HP_0100014—————11
Show 3 more
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‚£
Byooviz – Biogen
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Lucentis – Novartis
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Lucentis – Roche
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Cimerli – Coherus BioSciences
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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 13,531 documents
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Safety
Black-box Warning
Black-box warning for: Susvimo
Adverse Events
Top Adverse Reactions
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28,533 adverse events reported
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