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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02608918
Other study ID # 206301
Secondary ID AI468-065
Status Completed
Phase Phase 1
First received November 17, 2015
Last updated April 13, 2018
Start date January 5, 2016
Est. completion date May 24, 2016

Study information

Verified date April 2018
Source ViiV Healthcare
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to assess the taste properties of HIV inhibitor


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date May 24, 2016
Est. primary completion date May 24, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 80 Years
Eligibility For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com

Inclusion Criteria:

- Men and women of non-childbearing potential professional sensory panelists

- Aged between 25 and 80 years

Exclusion Criteria:

- History of relevant drug or food allergies, cardiovascular or Central nervous system (CNS) disease, clinically significant pathology, history of mental illness

- Positive HIV test

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
BMS-955176


Locations

Country Name City State
United States GSK Investigational Site Woburn Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
ViiV Healthcare Senopsys, LLC

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Taste properties of HIV Inhibitor will be measured using the Flavor Profile of the Flavor Leadership Criteria Up to 2 years
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