At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomized, Single-Center, Double-Blind, Placebo-Controlled, Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of a Single Oral Dose of TAK-792 in Healthy Subjects
In Brief
A Phase 1 clinical trial evaluating TAK-792 30 mg, TAK-792 30 mg placebo, and 10 other interventions for Healthy Male Adults Participants. Completed, enrolled 72 participants across 1 site.
Detailed Summary
The purpose of this study is to characterize the safety and tolerability profile of TAK-792 when administered as a single oral dose in healthy Japanese and Caucasian male participants.
Study Details
Timeline
Interventions
TAK-792 30 mg was administered in the morning after a fast.
TAK-792 30 mg placebo was administered in the morning after a fast.
TAK-792 100 mg was administered in the morning after a fast.
TAK-792 100 mg placebo was administered in the morning after a fast.
TAK-792 250 mg was administered in the morning after a fast.
TAK-792 250 mg placebo was administered in the morning after a fast.
TAK-792 500 mg was administered in the morning after a fast or after breakfast.
TAK-792 500 mg placebo was administered in the morning after a fast or after breakfast.
TAK-792 750 mg was administered in the morning after a fast.
TAK-792 750 mg placebo was administered in the morning after a fast.
TAK-792 1250 mg was administered in the morning after a fast.
TAK-792 1250 mg placebo was administered in the morning after a fast.