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  • NCT04267393

Active, Not Recruiting

Safety and Effectiveness of BMS-986263 in Adults With Compensated Cirrhosis (Liver Disease) From Nonalcoholic Steatohepatitis (NASH) - IM025-017

Oppdatert: 9 januar, 2024   |   ClinicalTrials.gov

Utskriftsvennlig Sammendrag

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Skriv ut denne siden IM025-017
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Vis detaljer

  • Phase 2

    Fase

  • Kjønn

  • 21-75

    Aldersgruppe

  • Active, Not Recruiting

Behandlingsalternativer

Studiearmer
TILDELT INTERVENSJON
Experimental: Dose A BMS-986263
Drug: BMS-986263
Experimental: Dose B BMS-986263
Drug: BMS-986263
Placebo Comparator: Placebo
Other: Placebo

Nøkkelkriterier for kvalifikasjon

For more information regarding Bristol Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Participants with liver biopsy fibrosis score stage 4 performed within 6 months - Men and women must agree to follow methods of contraception Exclusion Criteria: - Worsening liver disease or any disease might compromise participant safety in the opinion of the investigator - Known immunocompromised status or any disease or condition which might compromise participant safety - Prior exposure to BMS-986263 - Clinically relevant abnormal physical examination, vital signs, ECG, or clinical laboratory tests - Hepatic decompensation Other protocol-defined inclusion/exclusion criteria apply

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Bivirkninger (uønskede hendelser) og andre rapporterbare hendelser er definert her
For å rapportere bivirkninger (uønskede hendelser) eller reklamere på et legemiddel: Medisinsk informasjon

MLTNO2000046