Mass Balance and Absolute Oral Bioavailability of [14C]VH4524184
A Phase 1, Open-Label, Single Dose Study to Assess the Absolute Bioavailability, Mass Balance, Pharmacokinetics, Metabolism, and Excretion of [14C]VH4524184 in Healthy Participants
ViiV Healthcare
9 participants
Jun 4, 2026
INTERVENTIONAL
Conditions
Summary
The purpose of the study is to assess the bioavailability, mass balance, pharmacokinetics, metabolism and excretion of radiolabeled (14C) VH4524184.
Eligibility
Plain Language Summary
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Interventions
One dose of VH4524184 is administered to participants at time zero on Day 1 (Period 1).
A radiolabelled microdose of \[14C\]VH4524184 is administered 2.5 hours after VH4524184 dose administration on Day 1 (Period1).
One dose of radiolabelled \[14C\]VH4524184 is administered to participants at Day 15 (Period 2).
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07636928