Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, Safety, and Tolerability of Lutikizumab in Chinese Participants

Study Identifier
M24-465
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete

Study Details

Medical Condition
  • Healthy Volunteer
  • Study Drug
  • Lutikizumab Dose A
  • Lutikizumab Dose B
  • Phase
    Phase 1
    Sex
    Female & Male
    Age
    18 - 60 Years

    Protocol Summary

    The purpose of this study is to compare the bioavailability of two different formulations of lutikizumab, and to assess adverse events (AEs) and how lutikizumab moves through the body in healthy Chinese participants.

    Study Locations

    Location
    Status
    Location
    Altasciences Clinical Los Angeles, Inc /ID# 260986
    Cypress, California, United States, 90630
    Status
    Not applicable
    Location
    Acpru /Id# 259029
    Grayslake, Illinois, United States, 60030
    Status
    Not applicable
    Location
    PPD Clinical Research Unit - Austin /ID# 260141
    Austin, Texas, United States, 78744
    Status
    Not applicable