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Terminated Phase 3 Interventional

A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-1)

ClinicalTrials.gov ID: NCT05306574

Public ClinicalTrials.gov record NCT05306574. 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 2, 2026, 9:10 PM 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled, 2-Stage Trial to Evaluate Efficacy and Safety of Telitacicept Compared to Placebo in Patients With Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-1)

Brief summary

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

The purpose of this study is to evaluate the efficacy and safety of telitacicept in the treatment of moderately to severely active SLE.

Study identification

NCT ID
NCT05306574
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vor Biopharma
Industry
Enrollment
91 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
12 Years to 70 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
Jun 19, 2022
Primary completion
Jan 5, 2025
Completion
Jan 5, 2025
Last update posted
Jan 8, 2026

2022 – 2025

United States locations

U.S. sites
12
U.S. states
6
U.S. cities
12
Facility City State ZIP Site status
Anniston, Alabama Site Anniston Alabama 36207
Mission Hills Site Mission Hills California 91345
Orange Site Orange California 92868
Thousands Oaks Site Thousand Oaks California 91360
Miami, FL Site Miami Florida 33014
Tampa, Florida Site Tampa Florida 33765
Wheaton, Maryland Site Wheaton Maryland 20902
Grand Blanc Site Grand Blanc Michigan 48439
Baytown Site Baytown Texas 77521
Colleyville, Texas Site Colleyville Texas 76034
Houston Site Houston Texas 77084
Waco Site Waco Texas 76710

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 66 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05306574, 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 Jan 8, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05306574 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →