Propiverine
Propiverine is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
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Trade Name
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Drug Products
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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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HCPCS
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Clinical
Clinical Trials
13 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Overactive urinary bladder | D053201 | EFO_1000781 | N32.81 | — | 1 | 4 | 2 | 4 | 11 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Urinary incontinence | D014549 | HP_0000020 | R32 | — | — | 2 | — | 1 | 3 |
Urologic diseases | D014570 | N39.9 | — | — | 1 | — | — | 1 | |
Neurogenic urinary bladder | D001750 | HP_0000011 | N31 | — | — | 1 | — | — | 1 |
Indications Phases 2
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Indications Phases 1
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Interstitial cystitis | D018856 | EFO_1000869 | N30.1 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | PROPIVERINE |
INN | propiverine |
Description | Propiverine is a diarylmethane. |
Classification | Small molecule |
Drug class | spasmolytic agents (papaverine type) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CCCOC(C(=O)OC1CCN(C)CC1)(c1ccccc1)c1ccccc1 |
Identifiers
PDB | — |
CAS-ID | 60569-19-9 |
RxCUI | 55175 |
ChEMBL ID | CHEMBL1078261 |
ChEBI ID | 8493 |
PubChem CID | 4942 |
DrugBank | DB12278 |
UNII ID | 468GE2241L (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 407 documents
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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91 adverse events reported
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