Study to Assess the Effect of Acid-reducing Agent Famotidine on the Drug Levels of BMS-986256 in Healthy Participants
NCT ID: NCT04470778
Last Updated: 2025-02-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
35 participants
INTERVENTIONAL
2020-07-20
2021-03-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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BMS-986256
BMS-986256
Specified dose on specified days
BMS-986256 + Famotidine
BMS-986256
Specified dose on specified days
Famotidine
Specified dose on specified days
Interventions
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BMS-986256
Specified dose on specified days
Famotidine
Specified dose on specified days
Eligibility Criteria
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Inclusion Criteria
* Weight ≥ 50 kg and body mass index (BMI) between 18.0 kg/m2 and 32.0 kg/m2 inclusive at screening
* Women and men must agree to follow specific methods of contraception, if applicable, while participating in the trial
Exclusion Criteria
* Any significant acute or chronic medical illness
* Any major surgery within 4 weeks of study treatment administration
* Any other sound medical, psychiatric, and/or social reason as determined by the investigator
18 Years
55 Years
ALL
Yes
Sponsors
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Bristol-Myers Squibb
INDUSTRY
Responsible Party
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Principal Investigators
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Bristol-Myers Squibb
Role: STUDY_DIRECTOR
Bristol-Myers Squibb
Locations
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ICON (LPRA) - Salt Lake
Salt Lake City, Utah, United States
Countries
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Related Links
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BMS Clinical Trial Information
BMS Clinical Trial Patient Recruiting
Investigator Inquiry Form
FDA Safety Alerts and Recalls
Other Identifiers
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IM026-028
Identifier Type: -
Identifier Source: org_study_id
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