CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 50 enrolled
Drug / intervention
TAK-831 Tablet T2 +2 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.

Search/NCT03224325
NCT03224325Phase 1Completed

A Randomized, Investigator and Subject Blinded, Sponsor Unblinded Placebo-Controlled Phase I Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Escalating Multiple Doses of TAK-831 in Healthy Subjects

Neurocrine Biosciences·interventional·Posted Jul 21, 2017·Updated Jun 14, 2021

In Brief

A Phase 1 clinical trial evaluating TAK-831 Tablet T2, Placebo, and 1 other intervention for Healthy. Completed, enrolled 50 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the safety and tolerability of TAK-831 when administered as multiple oral doses at escalating dose levels in healthy participants.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
CollaboratorsTakeda

Timeline

Phase 1CompletedFinished
201820192020202120222023202420252026
First PostedJul 21, 2017
Enrollment StartJul 21, 2017
Primary CompletionSep 9, 2018
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 8.9 years ago

Interventions

TAK-831 Tablet T2drug

Tak-831 tablets.

Placebodrug

TAK-831 placebo-matching suspension.

TAK-831 Suspensiondrug

TAK-831 Suspension.