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Drug ReportsClopenthixol
Clopenthixol
Clopenthixol is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Clinical
Drug
Target
Variants
Financial
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Events Timeline
5D
1M
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6M
YTD
1Y
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5Y
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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
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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
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Indications
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Agency Specific
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Patent Expiration
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ATC Codes
N: Nervous system drugs
N05: Psycholeptics
N05A: Antipsychotics
N05AF: Thioxanthene derivatives, antipsychotic
N05AF05: Zuclopenthixol
HCPCS
No data
Clinical
Clinical Trials
10 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
SchizophreniaD012559EFO_0000692F2011
Indications Phases 1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameClopenthixol
INNzuclopenthixol
Description
Clopenthixol is a thioxanthene derivative having a chloro substituent at the 2-position and an alkylidene group at the 10-position with undefined double bond stereochemistry. It has a role as a H1-receptor antagonist, a serotonergic antagonist, an alpha-adrenergic antagonist, a dopaminergic antagonist and a first generation antipsychotic. It is a N-alkylpiperazine, a primary alcohol and a member of thioxanthenes.
Classification
Small molecule
Drug classTypical antipsychotic
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Structure (InChI/SMILES or Protein Sequence)
OCCN1CCN(CC/C=C2/c3ccccc3Sc3ccc(Cl)cc32)CC1
Identifiers
PDB
CAS-ID53772-83-1
RxCUI
ChEMBL IDCHEMBL53904
ChEBI ID
PubChem CID5311507
DrugBankDB01624
UNII ID47ISU063SG (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
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Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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3,287 adverse events reported
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