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A Phase 2, Open-Label, Single-Arm Trial of FT819 in Participants With Lupus Nephritis

NCT07570862 · Fate Therapeutics
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Official title
A Phase 2, Open-Label, Single-Arm Trial of FT819 in Participants With Refractory Moderate-to-Severe Systemic Lupus Erythematosus With Lupus Nephritis (RECLAIM-LN)
About this study
This is a multicenter, phase 2 single-arm trial designed to evaluate the efficacy and safety of FT819 in participants with moderate-to-severe systemic lupus erythematosus (SLE) with Class III/IV lupus nephritis (LN) (with or without concomitant Class V involvement) refractory to at least 2 immunosuppressive therapies prior to trial intervention. Participants will undergo a screening period of up to 28 days. Following screening, trial intervention will consist of bendamustine administration followed by a single dose of FT819. Efficacy, safety, and exploratory assessments will be conducted at predefined timepoints through Month 24 of post-treatment follow-up (PTFU). Following completion of these scheduled assessments, participants will continue in long-term follow-up (LTFU) for up to 15 years after FT819 administration to monitor ongoing safety and survival. Efficacy and disease activity will be assessed using standard LN measures, including complete renal response (CRR) and PRR (partial renal response), as well as clinician-reported outcomes, such as the SLEDAI-2K, BILAG, and PGA, performed at specified timepoints.
Eligibility criteria
INCLUSION CRITERIA: * Age ≥12 to ≤70 years * Diagnosis of SLE per EULAR/ACR 2019 classification criteria * Biopsy-proven proliferative Class III or IV LN, with or without concomitant Class V involvement, based on the 2003/2018 ISN/RPS classification * Positivity for at least one of the following autoantibodies at screening: 1. Antinuclear antibody (ANA) 2. Anti-double-stranded DNA (anti-dsDNA) or 3. Anti-Smith antibody * Active disease, defined as: a. Evidence of SLE activity, defined as either: i. SLEDAI-2K ≥6 or ii. At least 1 BILAG A or 2 BILAG B scores for SLE-related organ involvement; and b. Evidence of renal involvement, defined as UPCr ≥1 g/g; and c. Moderate-to-severe renal disease with investigator's impression that improvement is possible * Refractory to ≥2 systemic immunosuppressive therapies for the treatment of LN EXCLUSION CRITERIA: * Evidence of inadequate organ function during the screening period * Active central nervous system (CNS) symptoms attributable to autoimmune disease within 12 months prior to trial intervention * History of or current renal diseases (other than LN) that, in the opinion of the investigator, could interfere with assessment of LN or confound evaluation of disease activity * Receipt of dialysis (hemodialysis or peritoneal dialysis) within 12 weeks of trial intervention * Irreversible organ damage related to underlying disease (e.g., ESRD) where, in the opinion of the investigator, CD19 CAR T-cell therapy would be unlikely to benefit the participant * History of malignancy in the prior 5 years * Known allergy to the following FT819 components: albumin (human) or DMSO * History of intolerance or contraindication to bendamustine * Body weight \<30 kg * Any medical condition, clinical laboratory abnormality, or nonmedical/social issue that, per investigator or medical monitor judgement, precludes safe participation in and completion of the trial or that could affect compliance with protocol conduct or interpretation of results
Study design
Enrollment target: 53 participants
Allocation: na
Masking: none
Age groups: child, adult, older_adult
Timeline
Starts: 2026-07-27
Estimated completion: 2030-01-31
Last updated: 2026-09-14
Interventions
Biological: FT819
Primary outcomes
  • Complete Renal Response (CRR) at Week 26 (Week 26)
Sponsor
Fate Therapeutics · industry
Contacts & investigators
ContactFate Clinical Trials · contact · clinicaltrials@fatetherapeutics.com · 858-875-1800
ContactNatalie Shiff, MD · contact
All locations (12)
Wallace Rheumatic Studies CenterRecruiting
Beverly Hills, California, United States
Kaiser Permanente FontanaRecruiting
Fontana, California, United States
Providence Medical FoundationRecruiting
Fullerton, California, United States
University of California IrvineRecruiting
Irvine, California, United States
University of California San FranciscoRecruiting
San Francisco, California, United States
GNP ResearchRecruiting
Cooper City, Florida, United States
University of Florida Clinical Research CenterRecruiting
Gainesville, Florida, United States
Miami Dermatology and Laser ResearchRecruiting
Miami, Florida, United States
Nicklaus Children's HospitalRecruiting
Miami, Florida, United States
University of Nebraska Medical CenterRecruiting
Omaha, Nebraska, United States
Cross Creek Medical ClinicRecruiting
Fayetteville, North Carolina, United States
The University of Texas Southwestern Medical CenterRecruiting
Dallas, Texas, United States