At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 39 enrolled
Drug / intervention
TAK-648 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 1, Randomized, Double-Blind, Placebo- Controlled, Safety, Tolerability, and Pharmacokinetic Study of Escalating Single Oral TAK-648 Doses in Healthy Subjects
In Brief
A Phase 1 clinical trial evaluating TAK-648 and TAK-648 Placebo for Healthy Volunteers. Completed, enrolled 39 participants.
Detailed Summary
The purpose of this study is to determine the safety, tolerability and pharmacokinetics of TAK-648 when administered as a single oral dose of TAK-648 solution at escalating dose levels in healthy participants.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy Volunteers
Countries--
Collaborators--
Timeline
Phase 1CompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartAug 2014
Primary CompletionApr 2015
Study CompletionJul 2015
First PostedFeb 2016
TodayJul 2026
First PostedFeb 18, 2016
Enrollment StartAug 1, 2014
Primary CompletionApr 1, 2015
Study CompletionJul 1, 2015
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 10.4 years ago
Interventions
TAK-648drug
TAK-648 Solution
TAK-648 Placebodrug
TAK-648 placebo-matching solution