drugset / Trial / NCT03992014

Pharmacokinetics (PKs) and Metabolism of Radiolabelled Linerixibat

NCT03992014

Phase 1 Completed 6 enrolled GlaxoSmithKline
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Absorption, metabolism and excretion of linerixibat have been studied in previous clinical trials. However, no dedicated clinical studies of drug absorption, metabolism, and excretion have been conducted for linerixibat. The purpose of this study is to determine the PK, balance/excretion, and metabolism of radiolabeled 14 Carbon \[14C\]-linerixibat following a single intravenous (IV) radiolabeled microtracer dose (concomitant with a non-radiolabeled oral dose) and a single oral radiolabeled dose. This is a single group, two period, single sequence, and mass balance study will enroll 6 healthy male subjects. Each subject will be involved in the study for up to 10 weeks which includes screening period, two treatment periods (treatment Periods 1 and 2), separated by about 7 days (at least 13 days between oral doses), and a follow-up visit 1-2 weeks after the last assessment in treatment Period 2.

Timeline

Start
2019-07-08
Primary completion
2019-08-26
Completion
2019-08-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Linerixibat Small molecule 100 ug Intravenous
Subject Linerixibat Small molecule 90 mg Intravenous

Indications