A Study of Anti-CD19 Chimeric Antigen Receptor T-Cell Therapy, in Subjects With Refractory Generalized Myasthenia Gravis
- Conditions
- Myasthenia GravisGeneralized Myasthenia Gravis
- Interventions
- Biological: KYV-101Drug: Standard lymphodepletion regimen
- Registration Number
- NCT06193889
- Lead Sponsor
- Kyverna Therapeutics
- Brief Summary
A Study of the Anti-CD 19 Chimeric Antigen Receptor T Cell Therapy for Subjects with Myasthenia Gravis
- Detailed Description
Myasthenia gravis (MG) is a chronic autoimmune disease that affects the neuromuscular junction and is characterized by muscle weakness. B cells play a role in MG, and the disease is characterized by the presence of autoantibodies such as anti-AChR and anti-MuSK antibodies. CD-19 target chimeric antigen receptor (CAR) T cells harness the ability of cytotoxic T cells to directly and specifically lyse target cells to effectively deplete both normal and autoreactive B cells in the circulation as well as impacted lymphoid and potentially non-lymphoid tissues. KYV-101, a fully human anti-CD19 CAR T-cell therapy, will be investigated in adult subjects with myasthenia gravis (MG).
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 20
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description KYV-101 CAR-T cells with lymphodepletion conditioning KYV-101 Dosing with KYV-101 CAR-T cells KYV-101 CAR-T cells with lymphodepletion conditioning Standard lymphodepletion regimen Dosing with KYV-101 CAR-T cells
- Primary Outcome Measures
Name Time Method Incidence of adverse events (AEs) and laboratory abnormalities 2 years Efficacy of KYV-101 via Myasthenia Gravis Activities of Daily Living (MG-ADL) total score 24 weeks
- Secondary Outcome Measures
Name Time Method Efficacy of KYV-101 via quantitative myasthenia gravis (QMG) score 12, 24, and 52 weeks Efficacy of KYV-101 via Myasthenia Gravis Composite (MGC) score 12, 24, and 52 weeks Disease-related antibodies via levels of anti acetylcholine receptor (anti-AchR) Up to 2 years Disease-related antibodies via levels of anti muscle-specific tyrosine kinase (anti-MuSK) antibodies Up to 2 years Disease-related antibodies via levels of anti lipoprotein-related protein 4 (anti-LRP4) antibodies Up to 2 years To characterize Pharmacokinetics (PK) via chimeric antigen receptor positive (CAR-positive) T cell counts Up to 2 years To characterize Pharmacodynamics (PD) via B cell counts Up to 2 years To characterize Pharmacodynamics (PD) via systemic cytokine concentrations Up to 2 years To evaluate the Immunogenicity (humoral response) of KYV-101 (percentage of participants who develop anti-KYV-101 antibodies by immunoassays) Up to 2 years To assess PRO (Patient Outcome Rate) after infusion of KYV-101 Up to 2 years Change from baseline in in Myasthenia Gravis Quality of Life- 15 Revised (MGQOL15r)
To assess PRO (Patient Reported Outcome) after infusion of KYV-101 Up to 2 years Change from baseline in EQ-5D (Quality of Life developed by the EuroQol Group)
Trial Locations
- Locations (10)
University of Miami
🇺🇸Miami, Florida, United States
Universitätsklinik Magdeburg
🇩🇪Magdeburg, Germany
University of California, Irvine
🇺🇸Orange, California, United States
Stanford University Medical Center
🇺🇸Palo Alto, California, United States
Intermountain Medical Center
🇺🇸Murray, Utah, United States
Charite- Universitätsklinikum Berlin
🇩🇪Berlin, Germany
Universitätsklinikum der Ruhr-Universität Bochum
🇩🇪Bochum, Germany
Universitätsklinikum Hamburg-Eppendorf
🇩🇪Hamburg, Germany
Medizinische Hochscule Hannover
🇩🇪Hannover, Germany
Friedrich-Schiller-Universität Jena
🇩🇪Jena, Germany