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  • NCT05963932

Recruiting

A Study to Assess the Bioavailability and Effect of Food of BMS-986419 Immediate-release Tablet Formulation in Healthy Adult Participants - CN007-1001

Updated: 28 August, 2023   |   ClinicalTrials.gov

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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18-55

    Age Range

  • 1

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Treatment A: BMS-986419 DR Capsule - Fasted
Drug: BMS-986419 DR Capsule
Experimental: Treatment B: BMS-986419 IR Tablet - Fasted
Drug: BMS-986419 IR Tablet
Experimental: Treatment C: BMS-986419 IR Tablet - Fed
Drug: BMS-986419 IR Tablet
Experimental: Treatment D: BMS-986419 Crushed IR Tablet - Fed
Drug: BMS-986419 IR Tablet

Key Eligibility Criteria

Inclusion Criteria: - Healthy male and female participants without clinically significant deviation from normal, as determined by the investigator, in medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory evaluations. - Body mass index (BMI) of 18.0 to 32.0 kilograms per meter squared (kg/m^2), inclusive, and body weight ≥ 50 kg. - A female participant is eligible to participate if she is a woman not of childbearing potential (WNOCBP) Exclusion Criteria: - Any significant acute or chronic medical illness (eg, history of intracranial or intraspinal hemorrhage, CNS lesions, recent bacterial or fungal meningitis, etcetera) as determined by the investigator. - Current or recent (within 3 months of study intervention administration) gastrointestinal disease that could affect the absorption, distribution, metabolism, and excretion of study intervention (for example, bariatric procedure). - History of Gilbert's syndrome. - Women who are of childbearing potential and women who are breastfeeding.

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