Evidence mapPaperPMID 41514038Full record

Trial reportNature medicine2026

BCMA-directed mRNA CAR T cell therapy for myasthenia gravis: a randomized, double-blind, placebo-controlled phase 2b trial.

Tuan Vu, Hacer Durmus, Michael Rivner, Sheetal Shroff, Thomas Ragole, Bennett Myers, Mamatha Pasnoor, George Small, Chafic Karam, Mithila Vullaganti and 21 more

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Nature medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04146051 (Autologous T-Cells Expressing A Chimeric Antigen Receptor Directed To B-Cell Maturation Antigen), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04146051 phase2active not recruitingnot on this map

Autologous T-Cells Expressing A Chimeric Antigen Receptor Directed To B-Cell Maturation Antigen (BCMA) In Patients With Generalized Myasthenia Gravis (MG)

TypeinterventionalSponsorCartesian TherapeuticsRan2019 to 2026Enrolled30ConditionsMyasthenia Gravis, GeneralizedArmsDescartes-08
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Towards mRNA therapeutics 2.0.Nature reviews. Drug discovery · 2026
    Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Tuan VuUniversity of South Florida, Tampa, FL, USA.ORCID http://orcid.org/0000-0003-0724-0210
Hacer DurmusIstanbul University, Istanbul, Turkey.
Michael RivnerAugusta University, Augusta, GA, USA.ORCID http://orcid.org/0000-0002-6135-035X
Sheetal ShroffHouston Methodist Hospital, Houston, TX, USA.ORCID http://orcid.org/0000-0002-6317-4951
Thomas RagoleUniversity of Colorado, Aurora, CO, USA.
Bennett MyersDent Neurologic Institute, Amherst, NY, USA.
Mamatha PasnoorUniversity of Kansas Medical Center, Kansas City, KS, USA.
George SmallAllegheny General Hospital, Pittsburgh, PA, USA.
Chafic KaramUniversity of Pennsylvania, Philadelphia, PA, USA.
Mithila VullagantiTufts University, Boston, MA, USA.
Amanda PeltierVanderbilt University, Nashville, TN, USA.
Gregory SahagianProfound Research, San Diego, CA, USA.ORCID http://orcid.org/0000-0002-3893-4920
Marc H FeinbergSFM Clinical Research LLC, Boca Raton, FL, USA.
Adam SlanksyNeurology Associates, PA, Maitland, FL, USA.
Carolina Barnett-TapiaToronto General Hospital, Toronto, Ontario, Canada.
Zaeem SiddiqiUniversity of Alberta, Edmonton, Alberta, Canada.
Kelly GwathmeyVirginia Commonwealth University, Richmond, VA, USA.
Michael A BadruddojaCenter for Neurosciences, Tucson, AZ, USA.
Hafsa KambohCartesian Therapeutics, Frederick, MD, USA.
Rachel N RuggerieCartesian Therapeutics, Frederick, MD, USA.ORCID http://orcid.org/0009-0008-2578-3028
Renee R FedakCartesian Therapeutics, Frederick, MD, USA.ORCID http://orcid.org/0000-0003-4284-9283
C Andrew StewartCartesian Therapeutics, Frederick, MD, USA.ORCID http://orcid.org/0000-0001-7936-447X
Metin KurtogluCartesian Therapeutics, Frederick, MD, USA.
Murat KalayogluCartesian Therapeutics, Frederick, MD, USA.
Michael SingerCartesian Therapeutics, Frederick, MD, USA.
Christopher M JewellCartesian Therapeutics, Frederick, MD, USA.ORCID http://orcid.org/0000-0002-6668-6928
Milos D MiljkovicCartesian Therapeutics, Frederick, MD, USA.
Mazen DimachkieUniversity of Kansas Medical Center, Kansas City, KS, USA.
Tahseen MozaffarUniversity of California, Irvine, Irvine, CA, USA.
James F HowardUniversity of North Carolina, Chapel Hill, NC, USA. howardj@neurology.unc.edu.ORCID http://orcid.org/0000-0002-7136-8617
MG-001 Study Team

Funding

Manufacturing RNA-based CAR T cells to combat autoantibody-associated autoimmune disorders (AAAD)R44NS137943 · CARTESIAN THERAPEUTICS, INC. · 2025 to 2025
$1.5M
NINDS NIH HHS R44 NS115426NINDS NIH HHS R44 NS137943
6 · The paper itself

Abstract

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 .

Indexed as

B-Cell Maturation AntigenMyasthenia GravisReceptors, Chimeric AntigenRNA, MessengerT-LymphocytesActivities of Daily LivingAdultAgedAutoantibodiesDouble-Blind MethodFemaleHumansMaleMiddle AgedTreatment OutcomeAutoantibodiesB-Cell Maturation AntigenReceptors, Chimeric AntigenRNA, MessengerTNFRSF17 protein, human

Identifiers

PMID41514038
PMCPMC13004676

What Socratic holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.