Study to Assess the Way the Body Absorbs, Distributes, Breaks Down and Eliminates Radioactive BMS-986256 in Healthy Male Participants
NCT ID: NCT04269356
Last Updated: 2022-01-10
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
8 participants
INTERVENTIONAL
2020-02-18
2021-03-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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BMS-986256
Milk of magnesia
Specified dose on specified days
BMS-986256
Specified dose on specified days
Interventions
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Milk of magnesia
Specified dose on specified days
BMS-986256
Specified dose on specified days
Eligibility Criteria
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Inclusion Criteria
* Males must agree to follow specific methods of contraception, if applicable, while participating in the trial
Exclusion Criteria
* History of any significant drug and/or food allergies
18 Years
55 Years
MALE
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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Covance - Clinical Pharmacology Services - Madison
Madison, Wisconsin, 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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IM026-023
Identifier Type: -
Identifier Source: org_study_id
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