A Phase IIa Study of ICG318 CAR-T in Refractory Systemic Lupus Erythematosus With or Without Lupus Nephritis
Condition(s) studied
Investigational drug(s) / intervention(s)
ICG318, BCMA-CD19-IL-15/IL-15 sushi Compound CAR T following lymphodepletion: Anti-BCMA, Anti-CD19 Compound CAR-T Cells
Study summary
This Phase IIa, open-label, single-arm study includes an initial Safety Run-In followed by dose expansion to evaluate the safety, tolerability, cellular kinetics, pharmacodynamics, and preliminary clinical activity of a single infusion of ICG318 in participants with refractory SLE, with or without LN. Participants will receive protocol-specified lymphodepletion followed by ICG318 at the recommended Phase 2 dose.
Eligibility
Primary outcome measure(s)
- Number of Adverse Events after ICG318 infusion — Starting day 0 and up to 1 year after ICG318 infusion.
Number of participants with Adverse Events (AEs), Serious Adverse Events (SAEs), Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESI), and Dose Limiting Toxicities (DLTs). - DORIS remission rate — Starting day 0 and assessed at 6 months, and 1 year after ICG318 infusion.
DORIS remission defined as no circulating autoantibodies (e.g. dsDNA, Smith etc.) detected, no SLE medications, and SLEDAI-2K score of 0-1 (down from severe 7-10).
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| University of Chicago | Chicago | Illinois | Not Yet Recruiting |
| New York Medical College | Hawthorne | New York | Not Yet Recruiting |
| NorthWell | New Hyde Park | New York | Recruiting |
| Fox Chase Cancer Center- Temple BMT | Philadelphia | Pennsylvania | Not Yet Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07328581 on ClinicalTrials.gov ↗ ← All trials in the USA