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
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Study Complete
Study Details
Medical Condition
Study Drug
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