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Clinical Trials in the USA / NCT06328777
Recruiting Phase 2/3

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

NCT06328777 · tracked via the Priya Life Science USA tracker
Sponsor
Cabaletta Bio
Phase
Phase 2/3
Started
2024-07-02
Last updated
2026-08-17

Condition(s) studied

Systemic SclerosisSclerodermaInterstitial Lung Diseases

Investigational drug(s) / intervention(s)

CABA-201CABA-201

CABA-201: Single intravenous infusion of CABA-201 at a single dose level following preconditioning with fludarabine and cyclophosphamide

CABA-201: Single intravenous infusion of CABA-201 at a single dose level following preconditioning with fludarabine and cyclophosphamide

Study summary

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

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
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, 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.

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Yale University New Haven Connecticut Recruiting
Mayo Clinic Florida Jacksonville Florida Recruiting
Northwestern Memorial Hospital Chicago Illinois Recruiting
The University of Chicago Medical Center Chicago Illinois Recruiting
University of Kansas Medical Center Kansas City Kansas Recruiting
University of Michigan Ann Arbor Michigan Recruiting
Mayo Clinic Rochester Rochester Minnesota Recruiting
Columbia University Irving Medical Center New York New York Recruiting
University of Rochester Rochester New York Recruiting
Duke University Durham North Carolina Recruiting

More Cabaletta Bio trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06328777 on ClinicalTrials.gov ↗ ← All trials in the USA