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Drug ReportsFoscarbidopa
Foscarbidopa
Vyalev (foscarbidopa) is a small molecule pharmaceutical. Foscarbidopa was first approved as Vyalev on 2024-10-16. It is used to treat parkinson disease in the USA.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
Combinations
Vyalev
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Foscarbidopa
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Foslevodopa
Tradename
Company
Number
Date
Products
VYALEVAbbVieN-216962 RX2024-10-16
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
vyalevNew Drug Application2024-10-16
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
parkinson diseaseEFO_0002508D010300G20
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
8 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Parkinson diseaseD010300EFO_0002508G202428
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameFoscarbidopa
INNfoscarbidopa
Description
Foscarbidopa is an L-tyrosine derivative that is carbidopa in which the hydroxy group at position 4' is replaced by a phosphonooxy group. It is a water-soluble prodrug of carbidopa which is used for the treatment of Parkinson's disease. It has a role as a prodrug and an antiparkinson drug. It is an O-phosphoamino acid, a L-tyrosine derivative and a non-proteinogenic L-alpha-amino acid. It is functionally related to a carbidopa (anhydrous).
Classification
Small molecule
Drug classdopamine receptor agonists; phosphoro-derivatives
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Structure (InChI/SMILES or Protein Sequence)
C[C@@](Cc1ccc(OP(=O)(O)O)c(O)c1)(NN)C(=O)O
Identifiers
PDB
CAS-ID1907685-81-7
RxCUI
ChEMBL IDCHEMBL4802240
ChEBI ID
PubChem CID121288738
DrugBankDB16171
UNII ID5NT8HCA4OO (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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12 adverse events reported
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