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NCT Number: NCT07391605

Descartes-08 in Autoantibody Myositis

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).

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

T13, Chapel Hill, North Carolina, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Descartes-08

Drug

Autologous T-cells expressing a chimeric antigen receptor (CAR) directed to B-Cell maturation antigen (BCMA)

Placebo

Other

Plasma-Lyte

Primary outcomes

  1. Major improvement of 2016 ACR/EULAR Total Improvement score

    Time frame: 24 weeks

    Proportion of participants in the Descartes-08 group compared with placebo who achieve major improvement marked by ≥60 point improvement on the 2016 ACR/EULAR Total Improvement Score (TIS)

Study contacts

Contact information is provided by the study sponsor or research team.

Vera MD

CONTACT

[email protected]

6172318085

Sponsors and collaborators

Lead sponsor

Cartesian Therapeutics

Industry

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Feb 6, 2026
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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