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Drug ReportsBrolucizumab
Beovu(brolucizumab)
Beovu (brolucizumab) is an antibody pharmaceutical. Brolucizumab was first approved as Beovu on 2019-10-07. It is used to treat wet macular degeneration in the USA. It has been approved in Europe to treat wet macular degeneration. 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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Novartis Pharmaceuticals
FDA Novel Drug Approvals 2019
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
Trade Name
FDA
EMA
Beovu
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)
Brolucizumab
Tradename
Proper name
Company
Number
Date
Products
Beovubrolucizumab-dbllNovartisN-761125 RX2019-10-07
2 products
Labels
FDA
EMA
Brand Name
Status
Last Update
beovuBiologic Licensing Application2024-11-01
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
wet macular degenerationEFO_0004683D057135—
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
S: Sensory organ drugs
— S01: Ophthalmologicals
— S01L: Ocular vascular disorder agents
— S01LA: Antineovascularisation agents
— S01LA06: Brolucizumab
HCPCS
Code
Description
J0179
Injection, brolucizumab-dbll, 1 mg
Clinical
Clinical Trials
58 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_0001365H35.30141361942
Wet macular degenerationD057135EFO_0004683—14105625
Macular edemaD008269————81312
EdemaD004487HP_0000969R60.9——6129
Retinal dystrophiesD058499HP_0000556————1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Vision disordersD014786HP_0000505H53.11——7—18
Low visionD015354————7—18
Choroidal neovascularizationD020256————2—24
Retinal diseasesD012164HP_0000479H35.9——2——2
Retinal vein occlusionD012170EFO_1001157H34.81——2——2
Pathologic neovascularizationD009389————2——2
Diabetic retinopathyD003930EFO_0003770———1——1
Retinal degenerationD012162HP_0001105———1——1
Eye diseasesD005128EFO_0003966H44——1——1
Vascular diseasesD014652EFO_0004264I77——1——1
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Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
MyopiaD009216EFO_0003927H52.1————11
UveitisD014605HP_0000554H20.9————11
InflammationD007249MP_0001845—————11
Retinal artery occlusionD015356EFO_1001154H34.1————11
VasculitisD014657HP_0002633—————11
Retinal vasculitisD031300EFO_1001156H35.06————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameBrolucizumab
INNbrolucizumab
Description
Brolucizumab sold under trade name Beovu among others, is a humanized single-chain antibody fragment for the treatment of neovascular (wet) age-related macular degeneration (AMD).
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL3707357
ChEBI ID—
PubChem CID—
DrugBankDB14864
UNII IDXSZ53G39H5 (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‚£
Beovu – Novartis
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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 1,057 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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3,144 adverse events reported
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