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Cerca in Study Connect
  • NCT06746402

Recruiting

A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of BMS-986278 and the Effects of BMS-986278 on Cardiac Repolarization in Healthy Participants - IM027-1012

Aggiornato: 7 marzo, 2025   |   ClinicalTrials.gov.

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SELEZIONI UNA LINGUA

Dettagli della sperimentazione

  • Phase 1

    Fase

  • Sesso

  • 18-55

    Fascia d'età

  • 2

    Sede/i

  • Recruiting

Opzioni di trattamento

Bracci dello studio
INTERVENTO ASSEGNATO
Experimental: Part A
Drug: BMS-986278, Placebo
Experimental: Part B1/B2 Treatment A
Drug: BMS-986278
Experimental: Part B1/B2 Treatment B
Drug: BMS-986278, Placebo
Experimental: Part B1/B2 Treatment C
Drug: Placebo
Experimental: Part B1/B2 Treatment D
Drug: Placebo, Moxifloxacin
Experimental: Part B3 Treatment A
Drug: BMS-986278
Experimental: Part B3 Treatment B
Drug: BMS-986278, Placebo
Experimental: Part B3 Treatment C
Drug: Placebo
Experimental: Part B3 Treatment D
Drug: Placebo, Moxifloxacin

Principali criteri di idoneità

Inclusion Criteria: - Female individuals not of childbearing potential (INOCBP) and males. - Healthy as determined by medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory assessments. - Body mass index (BMI) 18.0 to 32.0 kg/m2 , inclusive, for Parts A and B. Exclusion Criteria: - Any significant acute or chronic medical illness as determined by the investigator. - History of clinically relevant cardiac disease as determined by the investigator, symptomatic or asymptomatic arrhythmias, presyncope or syncopal episodes, or additional risk factors for ventricular arrhythmias. - Any significant history of disease of the cardiovascular system that in the opinion of the Investigator makes the participant unsuitable for enrollment into the study. - Other protocol-defined inclusion/exclusion criteria apply.

Ti consigliamo vivamente di contattare BMS per segnalare gli effetti collaterali (eventi avversi)
Qui vengono definiti gli effetti collaterali (eventi avversi) e altri eventi da segnalare
Segnala effetti collaterali (eventi avversi) o reclami sulla qualità del prodotto: informazioni mediche