Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Orange, California and other locations
Dates
study started
study ends around

Description

Summary

This is a randomized, double-blind, placebo-controlled phase 2 study to evaluate the efficacy, safety and tolerability of an autologous T-cells expressing a chimeric antigen receptor (CAR) directed to B-Cell maturation antigen (BCMA) in patients with autoantibody-mediated myositis, including antisynthetase syndrome (ASyS) and dermatomyositis (DM).

Official Title

A Randomized Double-Blind Placebo-Controlled Study to Evaluate Efficacy, Safety, and Tolerability of Descartes-08 in Patients With Dermatomyositis and Antisynthetase Syndrome

Keywords

Antisynthetase Syndrome, MYOSITIS, DESCARTES-08, MRNA CAR-T, TOTAL IMPROVEMENT SCORES, CDASI, Decartes-08

Eligibility

You can join if…

Open to people ages 18 years and up

  • Confirmed diagnosis of one of the following:

Dermatomyositis (DM): Probability score ≥55% on the 2017 EULAR/ACR (European Alliance of Associations of Rheumatology/ American College of Rheumatology) criteria for classification of dermatomyositis (corresponding to diagnosis of 'probable or definite' DM). OR Antisynthetase Syndrome (ASyS): Diagnosis based on ACR/EULAR Classification Criteria (1)."

  • Participants must have dermatomyositis or antisynthetase syndrome with muscle and/or skin involvement.
  • Refractory or intolerance to standard therapy.
  • Stable background immunosuppressive therapy for ≥8 weeks.
  • Adequate hematologic, renal, hepatic, and pulmonary function (SpO₂ ≥92% on room air).
  • Informed consent, compliance with visits, contraception, and vaccinations required.

You CAN'T join if...

  • Isolated interstitial lung disease (ILD) without muscle or skin involvement
    • Severe irreversible muscle damage or advanced weakness (e.g., wheelchair-bound).
    • Interstitial lung disease (ILD) requiring oxygen, severe pulmonary impairment (FVC ≤45%, DLCO ≤40%), or pulmonary hypertension.
    • Other inflammatory myopathies (PM, IMNM, IBM, cancer- or drug-induced myositis, overlap myositis except Sjögren's).
    • Other severe neuromuscular, cardiac, pulmonary, or systemic autoimmune diseases requiring immunosuppression.
    • Significant uncontrolled chronic illnesses or psychiatric conditions interfering with participation.
    • Pregnancy or lactation.
    • Recent use of prohibited immunosuppressants/biologics or investigational agents (per washout periods).
    • Live vaccination within 4 weeks.
    • History of primary immunodeficiency, organ or bone marrow transplant.
    • Active or uncontrolled infections: HBV, HCV, HIV, tuberculosis, or recurrent/severe infections.

Locations

  • University of California, Irvine accepting new patients
    Orange California 92868 United States
  • National Neuromuscular Research Institute accepting new patients
    Austin Texas 78759 United States
  • University of North Carolina accepting new patients
    Chapel Hill North Carolina 27599 United States
  • Brigham and Women's Hospital accepting new patients
    Boston Massachusetts 02115 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Cartesian Therapeutics
Links
Related Info
ID
NCT07391605
Phase
Phase 2 Antisynthetase Syndrome Research Study
Study Type
Interventional
Participants
Expecting 60 study participants
Last Updated