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Piritramide
Piritramide is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
N: Nervous system drugs
— N02: Analgesics
— N02A: Opioid analgesics
— N02AC: Diphenylpropylamine derivative analgesics
— N02AC03: Piritramide
HCPCS
No data
Clinical
Clinical Trials
9 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Postoperative painD010149G89.18———213
Colorectal neoplasmsD015179———2—2
Circulating neoplastic cellsD009360———2—2
Residual neoplasmD018365———1—1
Colonic neoplasmsD003110C18———1—1
Postoperative nausea and vomitingD020250EFO_0004888———1—1
PainD010146EFO_0003843R52———1—1
Indications Phases 3
No data
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
AnalgesiaD000698————11
Heart diseasesD006331EFO_0003777I51.9————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePIRITRAMIDE
INNpiritramide
Description
Piritramide is a nitrile.
Classification
Small molecule
Drug class—
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
N#CC(CCN1CCC(C(N)=O)(N2CCCCC2)CC1)(c1ccccc1)c1ccccc1
Identifiers
PDB—
CAS-ID302-41-0
RxCUI8354
ChEMBL IDCHEMBL559288
ChEBI ID—
PubChem CID9331
DrugBankDB12492
UNII ID4RP92LYZ2F (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 641 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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214 adverse events reported
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