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  • NCT06568458

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

Oppdatert: 16 desember, 2024   |   ClinicalTrials.gov

Utskriftsvennlig Sammendrag

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Skriv ut denne siden IM027-1026
Last ned Veiledning for studiedeltakere

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Vis detaljer

  • Phase 1

    Fase

  • Kjønn

  • 18-65

    Aldersgruppe

  • 1

    Sted(er)

  • Recruiting

Behandlingsalternativer

Studiearmer
TILDELT INTERVENSJON
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

Nøkkelkriterier for kvalifikasjon

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.

Vi anbefaler at du kontakter BMS for å rapportere bivirkninger.
Bivirkninger (uønskede hendelser) og andre rapporterbare hendelser er definert her
For å rapportere bivirkninger (uønskede hendelser) eller reklamere på et legemiddel: Medisinsk informasjon

MLTNO2000046