At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 1 Study to Assess Absolute Bioavailability of TAK-906 and to Characterize Mass Balance, Pharmacokinetics, Metabolism, and Excretion of [14C]-TAK-906 in Healthy Male Subjects
In Brief
A Phase 1 clinical trial evaluating TAK-906 Oral Capsule, [14C]-TAK-906 Intravenous Infusion, and 1 other intervention for Healthy Volunteers. Completed, enrolled 6 participants across 1 site.
Detailed Summary
The purpose of this study is to determine ABA of TAK-906 following single oral (capsule) administration of 50 milligram (mg) of TAK-906 and single intravenous (IV) microtracer dose administration of 100 microgram (μg) (approximately 1 microcurie \[μCi\]) of \[14C\]-TAK-906 in Period 1 (ABA), and to determine the mass balance of TAK-906 in urine and feces following a single oral (solution) administration of 50 mg (approximately 100 μCi) of \[14C\]-TAK-906 in Period 2 (absorption, distribution, metabolism, and elimination \[ADME\]).
Study Details
Timeline
Interventions
TAK-906 capsule.
\[14C\]-TAK-906 intravenous infusion.
\[14C\]-TAK-906 oral solution.