Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsPhase2/Phase3

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

Sponsor: Cabaletta Bio

NCT ID: NCT06154252

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
CABA-201 following preconditioning with fludarabine and cyclophosphamide (biological)
How long the study runs
Study runs about 55 months (dates as stated)
About the drug or intervention
CABA-201 following preconditioning with fludarabine and cyclophosphamide — biological: Single intravenous infusion of CABA-201 at a single dose level following preconditioning with fludarabine and cyclophosphamide
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
6 Years to 75 Years
Who
All
Number of participants
74
Started
2023-12-20
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for idiopathic inflammatory myopathy
  • • Phase2/Phase3 - 74 participants
  • • 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

Who can take part?

  • • Ages 6 Years to 75 Years
  • • Diagnosed with idiopathic inflammatory myopathy

Where?

  • • London - Kings College Hospital NHS Foundation Trust - Accepting Adult Patients
  • • London - University College London Hospitals NHS Foundation Trust - Accepting Adult Patients
  • • Manchester - Manchester Royal Infirmary - Accepting Adult Patients
  • • Salford - Salford Royal Hospital - Accepting Adult Patients

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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

More detail

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.

Idiopathic Inflammatory MyopathyDermatomyositisAnti-Synthetase SyndromeImmune-Mediated Necrotizing MyopathyJuvenile DermatomyositisJuvenile PolymyositisJuvenile Idiopathic Inflammatory Myopathy (JIIM)Juvenile Myositis

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 6 Years - 75 Years
  • Who can join: All genders

What the study is looking for

  • ✓Age ≥18 and ≤75
  • ✓A clinical diagnosis of IIM, based on the 2017 The European League Against Rheumatism/American College of...
  • ✓Diagnosis of DM, ASyS, or IMNM
  • ✓Presence of muscle weakness
  • ✓Other protocol-defined criteria apply.

Who cannot take part

  • ✗safety concern to leukapheresis
  • ✗History of anaphylactic or severe systemic reaction to fludarabine, cyclophosphamide or any of their metabolites
  • ✗Active infection requiring medical intervention at screening
  • ✗Significant lung or heart impairment
  • ✗Previous CAR T cell therapy
See the full criteria
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.

Where Is This Study? (4 UK sites)

Kings College Hospital NHS Foundation Trust - Accepting Adult Patients

London SE5 9RS, United Kingdom

Recruiting
Site contact (verified)
Patrick Gordon, PhD, FRCP, MBBSPrincipal Investigator
Rheumatology Research Team0207 848 0214Kch-tr.CRDresearch@nhs.net

University College London Hospitals NHS Foundation Trust - Accepting Adult Patients

London WC1N 3BG, United Kingdom

Recruiting
Site contact (verified)
Dr. Pedro Machado, FRCP, PhDPrincipal Investigator
Dr. Pedro Machado, FRCP, PhD020 3456 7890uclh.car-ttrials@nhs.net

Manchester Royal Infirmary - Accepting Adult Patients

Manchester M13 9WL, United Kingdom

Recruiting
Site contact (verified)
Eleni Tholouli, MD, PhD, MRCP(UK), FRCPathPrincipal Investigator
Eleni Tholouli, MD, PhD, MRCP(UK), FRCPath01612765052Eleni.Tholouli@mft.nhs.uk

Salford Royal Hospital - Accepting Adult Patients

Salford M6 8HD, United Kingdom

Recruiting
Site contact (verified)
Hector Chinoy, PhD, FRCP, MSc, BMBS, BMedSciPrincipal Investigator

How to Get in Touch

Cabaletta Bio

Sponsor contact

CONTACT

267-759-3100 clinicaltrials@cabalettabio.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-09