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CompletedNCT02479308

A Study to Evaluate the Effect of ALKS 5461 on QT Intervals in Healthy Volunteers

The Effect of ALKS 5461 on QT Intervals in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
129 (actual)
Sponsor
Alkermes, Inc. · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study will evaluate the effects of ALKS 5461 on QT intervals in healthy volunteers as well as evaluate the safety and tolerability of ALKS 5461.

Conditions

Interventions

TypeNameDescription
DRUGMoxifloxacinSingle administration
DRUGALKS 5461Daily administration for a total of 12 dosing days
DRUGPlaceboPlacebo will be matched to Moxifloxacin or ALKS 5461

Timeline

Start date
2015-06-01
Primary completion
2015-10-01
Completion
2015-10-01
First posted
2015-06-24
Last updated
2015-11-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02479308. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Effect of ALKS 5461 on QT Intervals in Healthy Volunteers (NCT02479308) · Clinical Trials Directory