drugset / Trial / NCT05866861

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

NCT05866861 ↗

Phase 1 Completed 40 enrolled Cugene Inc.
RandomizedSequentialQuadruple-blindTreatment

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).

Timeline

Start
2023-04-24
Primary completion
2025-04-01
Completion
2025-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject CUG252 Unknown — Subcutaneous