Fezolinetant
Veozah (fezolinetant) is a small molecule pharmaceutical. Fezolinetant was first approved as Veozah on 2023-05-12. The pharmaceutical is active against neuromedin-K receptor.
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Therapeutic Areas
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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 |
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VEOZAH | Astellas Pharma | N-216578 RX | 2023-05-12 | 1 products, RLD, RS |
Labels
FDA
EMA
Brand Name | Status | Last Update |
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veozah | New Drug Application | 2023-05-09 |
Indications
FDA
EMA
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Agency Specific
FDA
EMA
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ATC Codes
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HCPCS
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Clinical
Clinical Trials
15 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 |
---|---|---|---|---|---|---|---|---|---|
Hot flashes | D019584 | — | 3 | 6 | — | — | 9 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Menopause | D008593 | EFO_0003922 | N95 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | 6 | — | — | — | — | 6 | ||
Hepatic insufficiency | D048550 | 1 | — | — | — | — | 1 | ||
Renal insufficiency | D051437 | HP_0000083 | N19 | 1 | — | — | — | — | 1 |
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | FEZOLINETANT |
INN | fezolinetant |
Description | Fezolinetant, sold under the brand name Veozah, is a medication used for the treatment of hot flashes (vasomotor symptoms) due to menopause. It is a small-molecule, orally active, selective neurokinin-3 (NK3) receptor antagonist which is under development by for the treatment of sex hormone-related disorders. It is developed by Astellas Pharma which acquired it from Ogeda (formerly Euroscreen) in April 2017.
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Classification | Small molecule |
Drug class | tachykinin (neurokinin) receptor antagonists: NK3 receptor antagonists |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Cc1nsc(-c2nnc3n2CCN(C(=O)c2ccc(F)cc2)[C@@H]3C)n1 |
Identifiers
PDB | — |
CAS-ID | 1629229-37-3 |
RxCUI | — |
ChEMBL ID | CHEMBL3608680 |
ChEBI ID | — |
PubChem CID | 117604931 |
DrugBank | DB15669 |
UNII ID | 83VNE45KXX (ChemIDplus, GSRS) |
Target
Agency Approved
TACR3
TACR3
Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
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Additional graphs summarizing 38 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
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0 adverse events reported
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