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Recruiting

An Investigational Study of Experimental Medication BMS-986231 Given in Participants With Different Levels of Liver Function - CV013-026

Actualizada: 28 August, 2018   |   ClinicalTrials.gov

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Detalles del estudio

  • Phase 1

    Fase

  • Géneros

  • 18-70

    Rango de edad

  • Recruiting

Opciones de tratamiento

Brazos del estudio
INTERVENCIÓN ASIGNADA
Experimental: Mild hepatic impairment
Drug: BMS-986231
Experimental: Moderate hepatic impairment
Drug: BMS-986231
Experimental: Normal hepatic function
Drug: BMS-986231
Experimental: Severe hepatic impairment
Drug: BMS-986231

Criterios clave de elegibilidad

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Body weight ≥ 45 kg and ≤ 120 kg and BMI ≥ 18 kg/m2 and ≤ 35 kg/m2 - Heart rate ≥ 50 bpm and < 95 bpm - Women of childbearing potential must have a negative urine or serum pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]) within 24 hours prior to the start of study treatment Exclusion Criteria: - Clinically relevant abnormal medical history, abnormal findings on physical examination, vital signs, ECG, or laboratory tests at Screening that the investigator judges as likely to interfere with the objectives of the trial or the safety of the volunteer - History of chronic headaches (defined as occurring 15 days or more a month, over the previous 3 months), headaches related to caffeine withdrawal (ie, coffee, soda, tea, energy drinks, etc.), or moderately severe to severe headaches - History of migraine or cluster headaches Other protocol defined inclusion/exclusion criteria could apply

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