BCMA-directed mRNA CAR T cell therapy for myasthenia gravis: a randomized, double-blind, placebo-controlled phase 2b trial
Myasthenia gravis (MG) is driven by the secretion of autoantibodies from pathogenic B cell maturation antigen (BCMA)-expressing plasma cells. In this phase 2b randomized, controlled, double-blind trial, we evaluated Descartes-08, an autologous BCMA-directed mRNA chimeric antigen receptor T cell therapy, in patients with generalized MG (gMG). Patients (n = 26) were randomly allocated to receive once-weekly intravenous infusions of Descartes-08 (n = 15) or placebo (n = 11) over 6 weeks. The primary endpoint was a ≥5-point improvement in the MG Composite (MGC) score at month 3. Secondary endpoints included the mean change from baseline in MGC, MG Activities of Daily Living (MG-ADL) and Quantitative MG (QMG) scores by month 12. At month 3, the proportion of patients achieving a ≥5-point improvement in the MGC score was significantly higher for those treated with Descartes-08 compared to placebo in the overall population (66.7% (n = 10/15) versus 27.3% (n = 3/11), P = 0.0472) and in a subpopulation of those positive for autoantibodies to the acetylcholine receptor (63.6% (n = 7/11) versus 12.5% (n = 1/8), P = 0.0258). For patients treated with Descartes-08, the changes from baseline in mean MGC, MG-ADL and QMG scores at month 4 were -7.1, -5.5 and -4.8, respectively, with 83.0% of patients achieving a sustained and clinically meaningful response at month 12. Notably, 33.0% of patients achieved minimum symptom expression (MSE) (MG-ADL score ≤1) by month 6, which was sustained through month 12. Among biologic-naive patients, 55.60% achieved MSE by month 6, which was maintained through month 12 without additional treatment. Descartes-08 was generally safe and well tolerated. Infusion-related reactions were the most common adverse events reported (Descartes-08, 80.0% (n = 16/20); placebo, 56.3% (n = 9/16)). In summary, a single course of six once-weekly infusions of Descartes-08 was well tolerated and resulted in sustained clinically meaningful responses among patients with gMG. ClinicalTrials.gov identifier: NCT04146051 .
Authors
- Renee Fedak
- Tuan Vu (ORCID: https://orcid.org/0000-0003-0724-0210)
- Bennett H. Myers
- Michael H. Rivner (ORCID: https://orcid.org/0000-0002-6135-035X)
- Michael Badruddoja
- Metin Kurtoğlu
- Chafic Karam
- Hafsa Kamboh
- Thomas Ragole
- Amanda Peltier (ORCID: https://orcid.org/0000-0003-1097-7715)
- Miloš D. Miljković (ORCID: https://orcid.org/0000-0001-5848-6320)
- Mithila Vullaganti (ORCID: https://orcid.org/0000-0003-0673-7372)
- Murat V. Kalayoglu
- C. Andrew Stewart
- Gregory Sahagian
- Adam Slanksy
- Rachel N. Ruggerie
- George Small
- Kelly Gwathmey
- Sheetal Shroff
- Christopher M. Jewell
- Mazen Dimachkie
- Marc H. Feinberg
- Tahseen Mozaffar
- Mamatha Pasnoor
- James F. Howard
- Michael Singer
- on behalf the SPPiRE Study Research Team
Institutions
- University of North Carolina at Chapel Hill (US)
- Tufts University (US)
- University of North Carolina Health Care (US)
- University of Alberta (CA)
- Virginia Commonwealth University (US)
- Vanderbilt University (US)
- University of California, Irvine (US)
- Augusta University (US)
- University of South Florida (US)
- Allegheny General Hospital (US)
- Toronto General Hospital (CA)
- Boca Raton Regional Hospital (US)
- GlobalFoundries (United States) (US)
- Dent Neurologic Institute (US)
- Methodist Hospital (US)
- Center for Neurosciences (US)
- Neurology Associates (US)
- University of Kansas Medical Center (US)
- Cara Therapeutics (United States) (US)
- University of Colorado Anschutz Medical Campus (US)
- Istanbul University (TR)
- University of Pennsylvania (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- Nature Medicine
- Published
- 2026-01-09
- DOI
- https://doi.org/10.1038/s41591-025-04171-y
- Citations
- 3
- Primary Topic
- Myasthenia Gravis and Thymoma
- Type
- article
- Field-Weighted Citation Impact
- 117.46