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Obe-cel in Severe, Refractory Systemic Lupus Erythematosus (SLE) With Active Lupus Nephritis (LN)

NCT07053800

This study is recruiting at 3 US sites in 2 states, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this trial is to evaluate the efficacy and safety of obecabtagene autoleucel (obe-cel) administered once following lymphodepletion in participants with severe, refractory systemic lupus erythematosus (SLE) and active lupus nephritis (LN).

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Lupus Nephritis

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
12 to 65 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Autolus Limited
Last updated on ClinicalTrials.gov
August 24, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

New York · 2

  • Icahn School of Medicine at Mount Sinai · New York, NY
  • State University of New York Upstate Medical Center (SUNY) · Syracuse, NY

Texas · 1

  • Texas Transplant Institute · San Antonio, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.