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Completed Phase 1 Interventional

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

ClinicalTrials.gov ID: NCT05866861

Public ClinicalTrials.gov record NCT05866861. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 20, 2026, 3:34 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT05866861
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Cugene Inc.
Industry
Enrollment
40 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 23, 2023
Primary completion
Mar 31, 2025
Completion
Mar 31, 2025
Last update posted
Jun 23, 2026

2023 – 2025

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
Site 1001 Anniston Alabama 36207
Site 1011 La Jolla California 92037
Site 1002 Clearwater Florida 33765
Site 1009 Tampa Florida 33606
Site 1007 Lawrenceville Georgia 30046
Site 1010 Columbus Ohio 44106
Site 1005 Middleburg Heights Ohio 44130
Site 1003 Duncansville Pennsylvania 16635
Site 1006 Dallas Texas 75231
Site 1004 Mesquite Texas 75150
Site 1012 Seattle Washington 98195

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05866861, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2026 · Synced Sep 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05866861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →