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Drug ReportsMelperone
Melperone
Melperone is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
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
No data
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
No data
Patent Expiration
No data
ATC Codes
N: Nervous system drugs
N05: Psycholeptics
N05A: Antipsychotics
N05AD: Butyrophenone derivatives, antipsychotics
N05AD03: Melperone
HCPCS
No data
Clinical
Clinical Trials
4 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
Parkinson diseaseD010300EFO_0002508G2011
Psychotic disordersD011618F20.8111
Mental disordersD001523EFO_0000677F91.911
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 nameMelperone
INNmelperone
Description
1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-1-butanone is an aromatic ketone.
Classification
Small molecule
Drug classantianxiety agents/neuroleptics (4'-fluoro-4-piperidinobutyrophenone derivatives)
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Structure (InChI/SMILES or Protein Sequence)
CC1CCN(CCCC(=O)c2ccc(F)cc2)CC1
Identifiers
PDB
CAS-ID3575-80-2
RxCUI
ChEMBL IDCHEMBL1531134
ChEBI ID
PubChem CID15387
DrugBankDB09224
UNII IDJ8WA3K39B7 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 436 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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929 adverse events reported
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