A Study of Anti-CD19 Chimeric Antigen Receptor T Cell Therapy for Subjects With Refractory Lupus Nephritis
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by a wide spectrum of organ involvement and disease severity. Renal involvement (categorized as lupus nephritis \[LN\]) may occur in approximately 50% of SLE patients and is marked by proteinuria, microscopic hematuria, and varying degrees of renal insufficiency. B cells play a central role in the pathogenesis of SLE and LN, with autoantibodies developing as an early finding, and local, tissue resident B cells producing pathogenic autoantibodies and driving inflammation and tissue damage over time. CD19-targeted chimeric antigen receptor (CAR) T cells harness the ability of cytotoxic T cells to directly and specifically lyse target cells to effectively deplete B cells in the circulation and in lymphoid and potentially non-lymphoid tissues. KYV-101, a fully human anti-CD19 CAR T-cell therapy, will be investigated in adult subjects with refractory lupus nephritis.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
2
KYV-101 anti-CD19 CAR-T cell therapy
Standard lymphodepletion regimen
Charite- Universitätsklinikum Berlin
Berlin, Germany
Universitätsklinikum Carl Gustav Carus Dresden
Dresden, Germany
Universitätsklinikum Düsseldorf
Düsseldorf, Germany
Universitätsklinikum Erlangen
Erlangen, Germany
Incidence adverse events (AEs) and laboratory abnormalities (Phase 1 and Phase 2)
Time frame: Up to 2 years
Frequency of dose limiting toxicities (Phase 1)
Time frame: Up to 2 years
To characterize the pharmacokinetics (PK) (Phase 1 and 2)
Levels of KYV-101 CAR-positive T cells in the blood
Time frame: Up to 2 years
To characterize the pharmacokinetics (PK) (Phase 1 and 2)
Levels of KYV-101 CAR Transgene
Time frame: Up to 2 years
To characterize the pharmacodynamics (PD) (Phase 1 and 2)
Levels of B cells in the blood
Time frame: Up to 2 years
To characterize the pharmacodynamics (PD) (Phase 1 and 2)
Levels of systemic cytokine concentrations in serum
Time frame: Up to 2 months
To evaluate disease related biomarkers (Phase 1 and 2)
Levels of anti-double stranded DNA (anti-dsDNA) in serum
Time frame: Up to 2 years
To evaluate disease related biomarkers (Phase 1 and 2)
Levels of complement C3, C4 in serum
Time frame: Up to 2 years
To evaluate efficacy of KYV-101 (Phase 1 and 2)
Complete renal response rates (CRR)
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Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP
Frankfurt, Germany
Universitätsklinikum Hamburg-Eppendorf
Hamburg, Germany
Time frame: 12, 24, and 52 weeks
To evaluate efficacy of KYV-101 (Phase 1 and 2)
Time to Complete renal response (CRR)
Time frame: Up to 2 years
To evaluate efficacy of KYV-101 (Phase 1 and 2)
Time from first achieved Complete renal response (CRR) to disease worsening or end of study
Time frame: Up to 2 years
To evaluate the immunogenicity (humoral response) of KYV-101 (Phase 1 and 2)
Percentage of participants who develop anti-KYV-101 antibodies by immunoassays
Time frame: Up to 2 years
To access Patient Related Outcome (PRO) after infusion of KYV-101 (Phase 1 and 2)
Change from baseline in 36-Item Short Form Survey (SF-36)
Time frame: Up to 2 years
To access Patient Related Outcome (PRO) after infusion of KYV-101 (Phase 1 and 2)
Change from baseline in Functional Assessment of Chronic Illness Therapy-Fatigue Scale (FACIT-F)
Time frame: Up to 2 years
To access Patient Related Outcome (PRO) after infusion of KYV-101 (Phase 1 and 2)
Change from baseline in Lupus Quality of Life (Qol) Questionnaire
Time frame: Up to 2 years
To access Patient Related Outcome (PRO) after infusion of KYV-101 (Phase 1 and 2)
Change from baseline in Work Productivity and Activity Impairment (WPAI)
Time frame: Up to 2 years
To define the recommended Phase 2 dose (Phase 1)
Time frame: Up to 2 years