Taste Properties of HIV Inhibitor

Sponsor
ViiV Healthcare (Industry)
Overall Status
Completed
CT.gov ID
NCT02608918
Collaborator
Senopsys, LLC (Industry)
8
1
1
4.6
1.7

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
Phase 1

Study Design

Study Type:
Interventional
Actual Enrollment :
8 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
An Open-Label Taste Assessment of BMS-955176 in Healthy Subjects
Actual Study Start Date :
Jan 5, 2016
Actual Primary Completion Date :
May 24, 2016
Actual Study Completion Date :
May 24, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: BMS-955176

BMS-955176 specified dose on specified days

Drug: BMS-955176
Other Names:
  • HIV Maturation Inhibitor
  • Outcome Measures

    Primary Outcome Measures

    1. Taste properties of HIV Inhibitor will be measured using the Flavor Profile of the Flavor Leadership Criteria [Up to 2 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 GSK Investigational Site Woburn Massachusetts United States 01801

    Sponsors and Collaborators

    • ViiV Healthcare
    • Senopsys, LLC

    Investigators

    • Study Director: Viiv Clinical Trials, ViiV Healthcare

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    ViiV Healthcare
    ClinicalTrials.gov Identifier:
    NCT02608918
    Other Study ID Numbers:
    • 206301
    • AI468-065
    First Posted:
    Nov 20, 2015
    Last Update Posted:
    Apr 17, 2018
    Last Verified:
    Apr 1, 2018
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 17, 2018