drugset / Trial / NCT04814602

Single-dose PK Assessment of Oral Proglumide in Those With Hepatic Impairment

NCT04814602 ↗

Phase 0 Completed 11 enrolled Georgetown University
Non-randomizedParallel-groupOpen-labelOther

Summary

Proglumide is an oral cholecystokinin (CCK) receptor antagonist that has been shown in non-clinical studies to reverse hepatic fibrosis and decrease the incidence of hepatocellular carcinoma (HCC). Because of these potential beneficial properties, proglumide may be useful in decreasing the fibrosis and risk for HCC in those with cirrhosis. Although proglumide is safe in those with normal hepatic function, the pharmacokinetics have not been established in those that are hepatic impaired. The purpose of this study is to analyze proglumide blood levels and excretion in subjects with cirrhosis compared to health controls.

Timeline

Start
2021-03-30
Primary completion
2021-08-30
Completion
2022-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Proglumide Small molecule 400 mg Oral

Indications