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  • NCT07225647

Not Yet Recruiting

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

Updated: 4 November, 2025   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
Print this page and the trial guide to help you talk with your doctor.
Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.
Print this page IM027-1052
Download Study Participant’s Guide

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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18-65

    Age Range

  • 2

    Location(s)

  • Not Yet Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
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

Key Eligibility Criteria

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.

If you want to report a side effect, you can report directly to the Danish Medicines Agency via the website www.meldenbivirkning.dk
We recommend that you also contact BMS to report side effects.
Side effects and other reportable events are defined here
Report side effects or product quality complaints: Medical Information

466-DK-2200001