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COMPLETEDPhase 1

A Study to Evaluate the Drug Levels of Deucravacitinib From Tablets After Oral Administration in Healthy Participants

A Phase 1, Open-label, Crossover Study to Evaluate the Pharmacokinetics of Deucravacitinib (BMS-986165) Administered as Various Solid Tablet Formulations in Healthy Subjects

NCT04949269•Bristol-Myers Squibb

View on ClinicalTrials.gov

AI summary by Clareo Health

Generating AI summary...

Conditions

Healthy Participants

Interventions

Deucravacitinib

Famotidine

Locations

2

United States

Locations (2)

Quotient Sciences Miami

Miami, Florida, United States

PPD Development, LP

Austin, Texas, United States

Key Dates

Start Date

July 20, 2021

Primary Completion Date

January 3, 2022

Completion Date

January 3, 2022

Last Updated

March 11, 2022

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Sponsors

Lead Sponsor

Bristol-Myers Squibb

Full Eligibility Criteria

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 11, 2022Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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