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Recruiting

A Study to Assess the Extent of Drug Interaction Between BMS-986278 and Ninetedanib, the Relative Bioavailability of BMS-986278 in Tablet and the Effect That Food Has on BMS-986278 in Tablet Formulations in Healthy Participants - IM027-1026

Actualizada: 29 octubre, 2024   |   ClinicalTrials.gov

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Detalles del estudio

  • Phase 1

    Fase

  • Géneros

  • 18-65

    Rango de edad

  • 1

    Ubicación (es)

  • Recruiting

Opciones de tratamiento

Brazos del estudio
INTERVENCIÓN ASIGNADA
Experimental: Part I: Period A
Drug: Nintedanib
Experimental: Part I: Period B
Drug: BMS 986278
Experimental: Part I: Period C
Drug: Nintedanib, BMS 986278
Experimental: Part II: Period 1
Drug: BMS 986278
Experimental: Part II: Period 2
Drug: BMS 986278
Experimental: Part II: Period 3
Drug: BMS 986278
Experimental: Part III: Period 1
Drug: BMS 986278
Experimental: Part III: Period 2
Drug: BMS 986278

Criterios clave de elegibilidad

Inclusion Criteria: - Participants must be healthy males and females (INOCBP) - Participant must have Body mass index (BMI) of 18.0 kg/m2 through 32.0 kg/m2, inclusive. - Participant must have Body weight ≥ 50 kg Exclusion Criteria: - Participant must not have current or recent GI disease - Participant with evidence of organ dysfunction or any clinically significant deviation, as determined by investigator, from normal in physical examination, vital signs, 12-lead ECG, or clinical laboratory determinations beyond what is consistent with the target population. - Participant with prior exposure to BMS-986278 and exposure of any investigational drug or placebo within 4 weeks of study intervention administration. - Other protocol-defined Inclusion/Exclusion criteria apply.

Recomendamos encarecidamente que se comunique con BMS para informar los efectos secundarios (eventos adversos)
Los efectos secundarios (eventos adversos) y otros eventos reportables se definen aquí
Informe de efectos secundarios (eventos adversos) o quejas sobre la calidad del producto: información médica

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