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ACTIVE NOT RECRUITING
NCT05866861
PHASE1

A Study in Participants With Mild-to-moderate Systemic Lupus Erythematosus

Sponsor: Cugene Inc.

View on ClinicalTrials.gov

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

DRUG

CUG252

CUG252 will be administered by subcutaneous injection.

DRUG

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