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Drug ReportsSulthiame
Sulthiame
Sulthiame 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
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
N: Nervous system drugs
N03: Antiepileptics
N03A: Antiepileptics
N03AX: Other antiepileptics in atc
N03AX03: Sultiame
HCPCS
No data
Clinical
Clinical Trials
5 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
EpilepsyD004827EFO_0000474G40.91124
Rolandic epilepsyD01930511
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Obstructive sleep apneaD020181EFO_0003918G47.3311
Sleep apnea syndromesD012891HP_0010535G47.311
ApneaD001049HP_0002104R06.8111
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Epileptic syndromesD00007337611
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameSulthiame
INNsultiame
Description
Sultiame is an organic molecular entity.
Classification
Small molecule
Drug class
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
NS(=O)(=O)c1ccc(N2CCCCS2(=O)=O)cc1
Identifiers
PDB
CAS-ID61-56-3
RxCUI
ChEMBL IDCHEMBL328560
ChEBI ID32171
PubChem CID5356
DrugBankDB08329
UNII IDI00Q766CZ2 (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 545 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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215 adverse events reported
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