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Drug ReportsFezolinetant
Fezolinetant
Veozah (fezolinetant) is a small molecule pharmaceutical. Fezolinetant was first approved as Veozah on 2023-05-12. It is used to treat hot flashes in the USA. The pharmaceutical is active against neuromedin-K receptor.
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EMA approval date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
signs and symptoms pathological conditionsD013568
Trade Name
FDA
EMA
Veozah
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Fezolinetant
Tradename
Company
Number
Date
Products
VEOZAHAstellas PharmaN-216578 RX2023-05-12
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
veozahNew Drug Application2023-10-18
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
hot flashesD019584
Agency Specific
FDA
EMA
Expiration
Code
FEZOLINETANT, VEOZAH, ASTELLAS
2028-05-12NCE
Patent Expiration
Patent
Expires
Flag
FDA Information
Fezolinetant, Veozah, Astellas
94222992034-03-28DS, DPU-3622
99872742034-03-28U-3622
108367682034-03-28U-3621
88717612031-04-04DP
ATC Codes
G: Genito urinary system and sex hormones
G02: Other gynecologicals in atc
G02C: Other gynecologicals in atc
G02CX: Other gynecologicals in atc
G02CX06: Fezolinetant
HCPCS
No data
Clinical
Clinical Trials
18 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hot flashesD01958438112
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
MenopauseD008593EFO_0003922N9511
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients66
Hepatic insufficiencyD04855011
Renal insufficiencyD051437HP_0000083N1911
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameFezolinetant
INNfezolinetant
Description
Fezolinetant is a triazolopyrazine that is 5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine substituted by 3-methyl-1,2,4-thiadiazol-5-yl, 4-fluorobenzoyl and methyl groups at positions 3, 7, and 8R, respectively. It is a prescription medicine used to reduce moderate to severe vasomotor symptoms due to menopause. It has a role as a neurokinin-3 receptor antagonist. It is a member of monofluorobenzenes, a triazolopyrazine, a member of thiadiazoles, a member of benzamides and a tertiary carboxamide.
Classification
Small molecule
Drug classtachykinin (neurokinin) receptor antagonists: NK3 receptor antagonists
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Structure (InChI/SMILES or Protein Sequence)
Cc1nsc(-c2nnc3n2CCN(C(=O)c2ccc(F)cc2)[C@@H]3C)n1
Identifiers
PDB
CAS-ID1629229-37-3
RxCUI
ChEMBL IDCHEMBL3608680
ChEBI ID
PubChem CID117604931
DrugBankDB15669
UNII ID83VNE45KXX (ChemIDplus, GSRS)
Target
Agency Approved
TACR3
TACR3
Organism
Homo sapiens
Gene name
TACR3
Gene synonyms
NK3R, TAC3R
NCBI Gene ID
Protein name
neuromedin-K receptor
Protein synonyms
Neurokinin B receptor, neurokinin beta receptor, NK-3 receptor, NK-3R, NK3 receptor, Tachykinin receptor 3
Uniprot ID
Mouse ortholog
Tacr3 (21338)
neuromedin-K receptor (Q9JKN0)
Alternate
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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