Proglumide
Proglumide is a small molecule pharmaceutical. It is currently being investigated in clinical studies. It is known to target cholecystokinin receptor type A.
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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
EMA
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Indications
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Agency Specific
FDA
EMA
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Patent Expiration
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HCPCS
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Clinical
Clinical Trials
3 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 |
---|---|---|---|---|---|---|---|---|---|
Fibrosis | D005355 | 1 | 1 | — | — | — | 1 | ||
Pain | D010146 | EFO_0003843 | R52 | 1 | 1 | — | — | — | 1 |
Healthy volunteers/patients | — | 1 | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Liver cirrhosis | D008103 | EFO_0001422 | K74.0 | 1 | — | — | — | — | 1 |
Non-alcoholic fatty liver disease | D065626 | EFO_0003095 | K75.81 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | PROGLUMIDE |
INN | proglumide |
Description | Proglumide is a racemate composed of equal amounts of (R)- and (S)-proglumide. A non-selective CCK antagonist that was used primarily for treatment of stomach ulcers, but has been replaced by newer drugs. It has a role as a drug metabolite, a xenobiotic metabolite, a cholinergic antagonist, an anti-ulcer drug, a cholecystokinin antagonist, a gastrointestinal drug, a delta-opioid receptor agonist and an opioid analgesic. It contains a (R)-proglumide and a (S)-proglumide. |
Classification | Small molecule |
Drug class | cholecystokinin (CCK) antagonists, antiulcer, anxiolytic agent |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CCCN(CCC)C(=O)C(CCC(=O)O)NC(=O)c1ccccc1 |
Identifiers
PDB | — |
CAS-ID | 6620-60-6 |
RxCUI | 8730 |
ChEMBL ID | CHEMBL316561 |
ChEBI ID | 32058 |
PubChem CID | 4922 |
DrugBank | DB13431 |
UNII ID | EPL8W5565D (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
CCKAR
CCKAR
Variants
Clinical Variant
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Financial
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Trends
PubMed Central
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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1 adverse events reported
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