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  • NCT07226817

Recruiting

A Study to Assess the Relative Bioavailability of BMS-986435 and Food Effect on the BMS-986435 in Healthy Adult Participants - CV029-1024

Uppdaterad: 12 november, 2025   |   ClinicalTrials.gov

Utskriftsvänlig sammanfattning

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Använd broschyren ”Om att delta i en klinisk prövning” för att få vägledning om deltagandeprocessen i en klinisk prövning. Förstå de viktiga faktorerna som man måste tänka på före ett beslut och få hjälp med att formulera frågor till studiepersonalen.
Skriv ut den här sidan CV029-1024
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VÄLJ SPRÅK

Information om prövningen

  • Phase 1

    Fas

  • Kön

  • 18-60

    Åldersintervall

  • 1

    Platser

  • Recruiting

Behandlingsalternativ

Studiegrupper
TILLDELAD BEHANDLING
Experimental: Treatment A
Drug: BMS-986435
Experimental: Treatment B
Drug: BMS-986435
Experimental: Treatment C
Drug: BMS-986435
Experimental: Treatment D
Drug: BMS-986435
Experimental: Treatment E
Drug: BMS-986435
Experimental: Treatment F
Drug: BMS-986435
Experimental: Treatment G
Drug: BMS-986435

Viktiga kriterier för deltagandet

Inclusion Criteria - Participants must have a body weight of ≥ 45 kg and BMI between 18 and 32 kg/m2, inclusive - Participants must be healthy as determined by medical history, physical examination, vital signs, 12-lead electrocardiogram (ECG), clinical laboratory assessments - Participants must have documented left ventricular ejection fraction (LVEF) ≥ 60% and absence of significant cardiac abnormality at screening, as determined by local transthoracic echocardiogram (TTE) assessment - Other protocol-defined Inclusion/Exclusion criteria apply

Vi rekommenderar att du kontaktar BMS för att rapportera biverkningar.
Biverkningar (oönskade händelser) och andra rapporterbara händelser definieras här
För att rapportera biverkningar (oönskade händelser) eller reklamera ett läkemedel: Medicinsk information

466-SE-2100058