Recruiting
Phase 2

ICG318

Sponsor:

iCell Gene Therapeutics

Code:

NCT07328581

Conditions

Systemic Lupus Erythematosus (SLE)

Lupus Nephritis (LN)

Eligibility Criteria

Sex: All

Age: 16 - 70

Healthy Volunteers: Not accepted

Interventions

ICG318, BCMA-CD19-IL-15/IL-15 sushi Compound CAR T following lymphodepletion

Study Details

Brief 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.

Conditions

Systemic Lupus Erythematosus (SLE)

Lupus Nephritis (LN)

Study ID

NCT07328581

Start date

Sep, 2026

Status verified date

Sep, 2026

Completion date

Dec, 2028

Anticipated

Primary completion date

Dec, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 16 - 70

Healthy Volunteers: Not accepted

Key Inclusion Criteria:

1. Age 16-70 years at the time of signing the informed consent
2. Have a diagnosis of SLE by EULAR/ACR 2019 criteria for ≥6 months.
3. Have at least one of an antinuclear antibody, anti-double-stranded deoxyribonucleic acid (dsDNA), or elevated anti-Smith (Sm) antibody
4. Inadequate response to 2 prior standard of care therapies, used for at least three months
5. SLE Disease Activity Index 2000 (SLEDAI-2K) score of ≥7 at Screening
6. For LN cohort participants. Kidney biopsy result within 6 months prior to Screening indicating Class III or IV (alone or in combination with Class V).

Key Exclusion Criteria:

1. Any acute, severe lupus related flare that needs immediate treatment
2. History of antiphospholipid syndrome with thromboembolic event within 12 months
3. History or current diagnosis of any disease, condition or treatment that may confound clinical assessments in the study.
4. Has drug-induced SLE.
5. History of prior CAR-T therapy.
6. History of bone marrow/hematopoietic stem cell or solid organ transplant or planned receipt during the study period.
7. Recent serious or ongoing infection, or risk for serious infection, or acute or chronic infection
8. Receipt of a live/live-attenuated vaccine other than BCG within 8 weeks
9. History within the past year or current clinically significant central nervous system disease, including but not limited to cerebrovascular accident, seizures, severe brain injury, dementia, Parkinson's disease, cerebellar disease, or multiple sclerosis
10. Impaired cardiac function or clinically significant cardiac disease
11. End stage renal disease or severe liver disease
12. Breastfeeding/lactating or pregnant women or women who intend to become pregnant at any time during the study.

Study Design

Enrollment

20 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Single arm

Biologic drug infusion

Interventions

ICG318, BCMA-CD19-IL-15/IL-15 sushi Compound CAR T following lymphodepletion

Anti-BCMA, Anti-CD19 Compound CAR-T Cells

Primary outcome measure

  • Number of Adverse Events after ICG318 infusion [ Time Frame: Starting day 0 and up to 1 year after ICG318 infusion. ]
  • DORIS remission rate [ Time Frame: Starting day 0 and assessed at 6 months, and 1 year after ICG318 infusion. ]

Central Contacts and Locations

Central contacts

Locations

NorthWell

Recruiting

New Hyde Park, New York, United States, 11040

Contacts

More Information

Sponsor

iCell Gene Therapeutics

Last update posted

Sep 17, 2026

Last verified

Sep, 2026

Keywords

  • Lupus
  • autoimmune disease
  • CAR-T Cell
  • Refractory disease
  • CD19
  • BCMA
  • Lupus Nephritis (LN)
  • Systemic Lupus Erythrematosus (SLE)

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-18. This information was provided to ClinicalTrials.gov by iCell Gene Therapeutics on 2026-09-17.