Danavorexton
Danavorexton is a small molecule pharmaceutical. It is currently being investigated in clinical studies. It is known to target orexin receptor type 2.
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Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
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HCPCS
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Clinical
Clinical Trials
7 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Healthy volunteers/patients | — | 3 | — | — | — | — | 3 | ||
Narcolepsy | D009290 | EFO_0000614 | G47.4 | 2 | — | — | — | — | 2 |
Idiopathic hypersomnia | D020177 | G47.11 | 1 | — | — | — | — | 1 | |
Obstructive sleep apnea | D020181 | EFO_0003918 | G47.33 | 1 | — | — | — | — | 1 |
Sleep apnea syndromes | D012891 | EFO_0003877 | G47.3 | 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 | DANAVOREXTON |
INN | danavorexton |
Description | Danavorexton (developmental code name TAK-925) is a selective orexin 2 receptor agonist. It is a small-molecule compound and is administered intravenously. The compound was found to dose-dependently produce wakefulness to a similar degree as modafinil in a phase 1 clinical trial. As of March 2021, danavorexton is under development for the treatment of narcolepsy, idiopathic hypersomnia, and sleep apnea. It is related to another orexin receptor agonist known as TAK-994, the development of which was discontinued for safety reasons in October 2021.
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Classification | Small molecule |
Drug class | Orexin receptor agonist |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | COC(=O)N1CCC[C@H](NS(C)(=O)=O)[C@@H]1CO[C@H]1CC[C@@H](c2ccccc2)CC1 |
Identifiers
PDB | — |
CAS-ID | 2114324-48-8 |
RxCUI | — |
ChEMBL ID | CHEMBL4650341 |
ChEBI ID | — |
PubChem CID | 130310079 |
DrugBank | — |
UNII ID | 1QMD83K4YN (ChemIDplus, GSRS) |
Target
Agency Approved
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Variants
Clinical Variant
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Financial
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Trends
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Additional graphs summarizing 4 documents
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
0 adverse events reported
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