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Набира участници Фаза 1/2 NCT06328777

RESET-SSc: An Open-Label Study to Evaluate the Safety and Efficacy of CABA-201, a CD19-CAR T Cell Therapy, in Subjects With Systemic Sclerosis

Фаза 1/2 – комбинирано ранно изпитване
Заболявания: Systemic Sclerosis Scleroderma

Спонсор: Cabaletta Bio

Налично на: БГ
Обобщение
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
Описание
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.
Кой може да участва
Inclusion Criteria: * Age ≥18 and ≤75 * A clinical diagnosis of SSc, based on the 2013 American College of Rheumatology and European League Against Rheumatism classification criteria. * Early active disease * Evidence of significant skin, pulmonary, renal, or cardiac involvement Exclusion Criteria: * Contraindication to leukapheresis * History of anaphylactic or severe systemic reaction to fludarabine, cyclophosphamide or any of their metabolites * Active infection requiring medical intervention at screening visit * Current symptoms of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, pulmonary, psychiatric, cardiac, neurological, or cerebral disease, including severe and uncontrolled infections, such as sepsis and opportunistic infections. * Concomitant medical conditions that, in the opinion of the investigator, might place the subject at unacceptable risk for participation in this study, interfere with the assessment of the effects or safety of the investigational product or with the study procedures * Severe lung or cardiac impairment * Previous CAR T cell therapy * Prior solid organ (heart, liver, kidney, lung) transplant or hematopoietic cell transplant Other protocol-defined inclusion/exclusion criteria may apply.
Интервенции
CABA-201
BIOLOGICAL
Места на провеждане 10
САЩ (10)
University of Michigan
Ann Arbor , Michigan
Northwestern Memorial Hospital
Chicago , Illinois
The University of Chicago Medical Center
Chicago , Illinois
Duke University
Durham , North Carolina
Mayo Clinic Florida
Jacksonville , Florida
University of Kansas Medical Center
Kansas City , Kansas
Yale University
New Haven , Connecticut
Columbia University Irving Medical Center
New York , New York
Mayo Clinic Rochester
Rochester , Minnesota
University of Rochester
Rochester , New York
Технически детайли
Статус
Набира участници
Фаза
Фаза 1/2
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
75 Years
Здрави доброволци
Не
Начална дата
02.07.2024
Крайна дата
01.07.2029
Регистрационен номер
NCT06328777
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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