A Study in Healthy Japanese and Caucasian Subjects to Assess the Pharmacokinetics, Safety and Tolerability of Risankizumab

Study Identifier
M16-533
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Study Details

Medical Condition
  • Healthy Volunteer
  • Study Drug
  • Risankizumab
  • Placebo
  • Phase
    Phase 1
    Sex
    Male
    Age
    18 - 45 Years

    Protocol Summary

    The main objective of this study is to assess the pharmacokinetics, safety, tolerability and immunogenicity following a single intravenous (IV) infusion of risankizumab in healthy Japanese and Caucasian participants.

    Study Locations

    Location
    Status
    Location
    Altasciences Clinical Los Angeles, Inc /ID# 164197
    Cypress, California, United States, 90630
    Status
    Not applicable