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Not Yet Recruiting

A Study to Assess the Effect of Food on the Drug Levels of Admilparant - IM027-1052

Uppdaterad: 4 november, 2025   |   ClinicalTrials.gov

Utskriftsvänlig sammanfattning

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Använd broschyren ”Om att delta i en klinisk prövning” för att få vägledning om deltagandeprocessen i en klinisk prövning. Förstå de viktiga faktorerna som man måste tänka på före ett beslut och få hjälp med att formulera frågor till studiepersonalen.

Information om prövningen

  • Phase 1

    Fas

  • Kön

  • 18-65

    Åldersintervall

  • 2

    Platser

  • Not Yet Recruiting

Behandlingsalternativ

Studiegrupper
TILLDELAD BEHANDLING
Experimental: Part 1: Treatment A
Drug: Admilparant
Experimental: Part 1: Treatment B
Drug: Admilparant
Experimental: Part 2: Treatment C
Drug: Admilparant
Experimental: Part 2: Treatment D
Drug: Admilparant

Viktiga kriterier för deltagandet

Inclusion Criteria - Participants must have a body mass index (BMI) of 18.0 kg/m2 to 32.0 kg/m2, inclusive, at screening. - Participants must have a body weight of ≥ 50 kg for males and ≥ 45 kg for females at screening. Exclusion Criteria - Participants must not have any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the participant from participating in the study. - Participants must not have had any previous exposure to Admilparant. - Participants must not have a history of any severe drug allergy or drug reaction (such as anaphylaxis or hepatotoxicity). - Other protocol-defined Inclusion/Exclusion criteria apply.

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Biverkningar (oönskade händelser) och andra rapporterbara händelser definieras här
För att rapportera biverkningar (oönskade händelser) eller reklamera ett läkemedel: Medicinsk information

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