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Descartes-08 in Autoantibody Myositis

RecruitingPhase 2

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

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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.

About the study

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).

What is being tested

Sponsor: Cartesian Therapeutics · Participants: 60 · Started: Apr 28, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07391605

Locations in the U.S.

CaliforniaUniversity of California, Irvine, Orange
MassachusettsBrigham and Women's Hospital, Boston
North CarolinaUniversity of North Carolina, Chapel Hill
TexasNational Neuromuscular Research Institute, Austin

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.