Clinical Research Directory
Browse clinical research sites, groups, and studies.
A Study in Participants With Mild-to-moderate Systemic Lupus Erythematosus
Sponsor: Cugene Inc.
Summary
The main purpose of this study is to evaluate the safety and tolerability of CUG252 following multiple ascending doses in participants with Systemic Lupus Erythematosus (SLE).
Official title: A Phase Ib, Randomized, Double-Blind, Placebo-Controlled, Ascending-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered CUG252 Following Multiple Dose Administrations in Participants With Mild-to-Moderate SLE
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
40
Start Date
2023-04-24
Completion Date
2025-04-01
Last Updated
2025-02-20
Healthy Volunteers
No
Interventions
CUG252
CUG252 will be administered by subcutaneous injection.
Placebo
Placebo will be administered by subcutaneous injection.
Locations (11)
Site 1001
Anniston, Alabama, United States
Site 1011
La Jolla, California, United States
Site 1002
Clearwater, Florida, United States
Site 1009
Tampa, Florida, United States
Site 1007
Lawrenceville, Georgia, United States
Site 1010
Columbus, Ohio, United States
Site 1005
Middleburg Heights, Ohio, United States
Site 1003
Duncansville, Pennsylvania, United States
Site 1006
Dallas, Texas, United States
Site 1004
Mesquite, Texas, United States
Site 1012
Seattle, Washington, United States