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
For general inquiries, please contact
Study Complete
Study Details
Medical Condition
Study Drug
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