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Набира участници Фаза 2/3 NCT06154252

RESET-Myositis: An Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects With Active Idiopathic Inflammatory Myopathy or Juvenile Idiopathic Inflammatory Myopathy

Фаза 2/3 – комбинирано изпитване
Заболявания: Idiopathic Inflammatory Myopathy Dermatomyositis Anti-Synthetase Syndrome Immune-Mediated Necrotizing Myopathy Juvenile Dermatomyositis Juvenile Polymyositis Juvenile Idiopathic Inflammatory Myopathy (JIIM) Juvenile Myositis

Спонсор: Cabaletta Bio

Налично на: БГ
Обобщение
RESET-Myositis: Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects with Active Idiopathic Inflammatory Myopathy or Juvenile Idiopathic Inflammatory Myopathy
Описание
Idiopathic inflammatory myopathies (IIMs, or myositis) are a group of rare autoimmune diseases characterized by inflammation and muscle weakness. Though the cause of IIM is not well understood, some subtypes of IIM, including dermatomyositis (DM), anti-synthetase syndrome (ASyS), immune-mediated necrotizing myopathy (IMNM), and juvenile idiopathic inflammatory myopathy (JIIM), are thought to involve B cells that cause the body to attack different tissues in the body. This study is being conducted to evaluate the safety and efficacy of an investigational cell therapy, CABA-201, that can be given to patients with DM, ASyS, IMNM, or JIIM 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
Adult Cohorts Inclusion Criteria: * Age ≥18 and ≤75 * A clinical diagnosis of IIM, based on the 2017 The European League Against Rheumatism/American College of Rheumatology classification criteria * Diagnosis of DM, ASyS, or IMNM * Evidence of active disease, despite prior or current treatment with standard of care treatments, as defined by the presence of elevated creatine kinase (CK), DM rash, or active disease on muscle biopsy, magnetic resonance imaging (MRI), or electromyography * Presence of muscle weakness Other protocol-defined criteria apply. 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 * 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 * Significant lung or cardiac impairment * Previous CAR T cell therapy * Prior solid organ (heart, liver, kidney, lung) transplant or hematopoietic cell transplant Other protocol-defined criteria apply. Juvenile Cohort Inclusion Criteria: * Age ≥6 and ≤17 years at enrollment * A clinical diagnosis of IIM, based on the 2017 The European League Against Rheumatism/American College of Rheumatology classification criteria * Evidence of active disease, despite prior or current treatment with standard of care treatments, as defined by the presence of elevated muscle enzymes, DM rash, or active disease on muscle biopsy, magnetic resonance imaging (MRI), or electromyography Other protocol-defined criteria apply. 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 * 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 * Significant lung or cardiac impairment * Previous CAR T cell therapy * Prior solid organ (heart, liver, kidney, lung) transplant or hematopoietic cell transplant Other protocol-defined criteria apply.
Интервенции
CABA-201 following preconditioning with fludarabine and cyclophosphamide
BIOLOGICAL
Места на провеждане 34
Великобритания (4)
Kings College Hospital NHS Foundation Trust - Accepting Adult Patients
London
University College London Hospitals NHS Foundation Trust - Accepting Adult Patients
London
Dr. Pedro Machado, FRCP, PhD
Manchester Royal Infirmary - Accepting Adult Patients
Manchester
Eleni Tholouli, MD, PhD, MRCP(UK), FRCPath
Salford Royal Hospital - Accepting Adult Patients
Salford
САЩ (30)
University of Michigan - Accepting Young Adult and Juvenile Patients
Ann Arbor , Michigan
Children's Healthcare of Atlanta - Accepting Juvenile Patients
Atlanta , Georgia
Emory University - Accepting Adult Patients
Atlanta , Georgia
Children's Hospital Colorado - Accepting Juvenile Patients
Aurora , Colorado
National Institutes of Health - Accepting Adult and Juvenile Patients
Bethesda , Maryland
NOT_YET_RECRUITING
Boston Children's Hospital - Accepting Young Adults and Juvenile Patients
Boston , Massachusetts
University of North Carolina at Chapel Hill - Accepting Adult Patients
Chapel Hill , North Carolina
Ann & Robert H. Lurie Children's Hospital of Chicago - Accepting Young Adult and Juvenile Patients
Chicago , Illinois
Northwestern Memorial Hospital - Accepting Adult Patients
Chicago , Illinois
The University of Chicago Medical Center - Accepting Adult and Juvenile Patients
Chicago , Illinois
Dr. Iazsmin Ventura, MD - Adult patient contact
University of Texas Southwestern Medical Center - Accepting Juvenile Patients
Dallas , Texas
Dr. Samuel John
Duke University Medical Center - Accepting Young Adults and Juvenile Patients
Durham , North Carolina
Houston Methodist Hospital - Accepting Adult Patients
Houston , Texas
Amelia A. Nounes, MSN, RN, CCRP
University of Texas MD Anderson Cancer Center - Accepting Adult Patients
Houston , Texas
Christina Amos Briggs, BSN, RN
Mayo Clinic Florida - Accepting Adult Patients
Jacksonville , Florida
University of Kansas Medical Center - Accepting Adult Patients
Kansas City , Kansas
Children's Wisconsin Pediatric Rheumatology -Accepting Young Adult and Juvenile Patients
Milwaukee , Wisconsin
NOT_YET_RECRUITING
Erin Hammelev - Research Coordinator
Vanderbilt University Medical Center - Accepting Adult Patients
Nashville , Tennessee
Hospital for Special Surgery - Accepting Adult and Juvenile Patients
New York , New York
Memorial Sloan Kettering Cancer Center - Accepting Adult and Juvenile Patients
New York , New York
University of California Irvine - Accepting Adult Patients
Orange , California
Children's Hospital of Philadelphia - Accepting Young Adult and Juvenile Patients
Philadelphia , Pennsylvania
CARTintake@chop.edu
UPMC Children's Hospital of Pittsburgh - Accepting Juvenile Patients
Pittsburgh , Pennsylvania
NOT_YET_RECRUITING
UPMC Arthritis and Autoimmunity Center - Accepting Adult Patients
Pittsburgh , Pennsylvania
NOT_YET_RECRUITING
Laurie Hope - Research Coordinator
Oregon Health & Science University - Accepting Adult Patients
Portland , Oregon
Mayo Clinic - Accepting Adult Patients
Rochester , Minnesota
University of California, San Francisco Benioff Children's Hospital - Accepting Young Adult and Juvenile Patients
San Francisco , California
Seattle Children's Research Institute - Accepting Juvenile Patients
Seattle , Washington
Johns Hopkins All Children's Hospital - Accepting Juvenile Patients
St. Petersburg , Florida
Children's Hospital at Montefiore - Accepting Young Adult and Juvenile Patients
The Bronx , New York
Технически детайли
Статус
Набира участници
Фаза
Фаза 2/3
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
6 Years
Максимална възраст
75 Years
Здрави доброволци
Не
Начална дата
20.12.2023
Крайна дата
01.07.2028
Регистрационен номер
NCT06154252
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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