CABA-201
BiologicalSingle intravenous infusion of CABA-201 at a single dose level following preconditioning with fludarabine and cyclophosphamide
Other names: Rese-cel, Resecabtagene autoleucel
NCT Number: NCT06328777
RESET-SSc: A Phase 1/2 Open-Label Study to Evaluate the Safety and Efficacy of CABA-201, a CD19-CAR T cell therapy, in Subjects with Systemic Sclerosis
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Phase 2 / Phase 3
Yale University, New Haven, Connecticut, United States
Systemic sclerosis (SSc), also known as scleroderma , is a rare autoimmune disorder characterized by autoantibody production and abnormal B cell function. Though the cause of SSc is not well understood, it is thought to involve B cells that cause the body to attack different tissues in one's own body, causing skin and organ fibrosis. This study is being conducted to evaluate the safety and efficacy of an investigational therapy, CABA-201, a CD19-CAR T cell therapy, that can be given to patients with SSc who have active disease. A single dose of CABA-201 in combination with cyclophosphamide (CY) and fludarabine (FLU) will be evaluated.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other protocol-defined inclusion/exclusion criteria may apply.
Single intravenous infusion of CABA-201 at a single dose level following preconditioning with fludarabine and cyclophosphamide
Other names: Rese-cel, Resecabtagene autoleucel
Time frame: Up to 28 days after CABA-201 infusion
Incidence and severity of AEs
Time frame: Week 52
Mean change from baseline in % predicted FVC without any immunomodulatory or anti-fibrotic medications and on no or low dose of steroids
Time frame: Up to 156 weeks (Phase 1/2) and through 104 weeks (Sub-study)
Incidence and severity of AEs, including changes in laboratory values and vital signs
Time frame: Up to 156 weeks (Phase 1/2) and through 104 weeks (Sub-study)
Levels of B cells in the blood
Time frame: Up to 156 weeks (Phase 1/2) and through 104 weeks (Sub-study)
Levels of CABA-201-positive T cells in the blood
Time frame: Up to 156 weeks (Phase 1/2) and at Week 52 (Sub-study)
Proportion of subjects achieving revised Composite Response Index for Systemic Sclerosis (CRISS) criteria
Time frame: Week 52 (Sub-study)
Contact information is provided by the study sponsor or research team.
Cabaletta Bio
Industry
A Phase 1/2, Open-Label Study to Evaluate the Safety and Efficacy of Autologous CD19-specific Chimeric Antigen Receptor T Cells (CABA-201) in Subjects With Systemic Sclerosis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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