Active, not recruiting
Phase 3
Investigating an mRNA CAR T-cell Therapy, Known as Descartes-08, as a Potential Approach to Treat Myasthenia Gravis
Condition(s) studied
Myasthaenia Gravis
Investigational drug(s) / intervention(s)
Decartes-08Placebo Drug
Decartes-08: Autologous mRNA CAR T-cell therapy
Placebo Drug: infusion without Decartes-08
Study summary
The AURORA Study is evaluating the safety, tolerability, and efficacy of an investigational mRNA CAR T-cell therapy known as Descartes-08 in adults with acetylcholine receptor autoantibody -positive generalized myasthenia gravis. Part 1 of the study will last around 6 months. For eligible participants, Part 2 will last around 8 months.
Eligibility
Inclusion Criteria:
* Patient must be at least 18 years of age.
* Patient must have generalized myasthenia gravis (gMG), Myasthenia Gravis Foundation of America (MGFA) clinical classification grades 2-4 at the time of Sscreening.
* MG-Activities of Daily Living (MG ADL) total score ≥ 6.
* Concomitant immunosuppressive drugs must be deemed necessary by the investigator. The dose must be stable for a minimum of 8 weeks prior to Baseline visit.
* If a patient is using corticosteroids, the daily dose should not exceed 40 mg/day of prednisone equivalent. The dose must have been stable for a minimum of 8 weeks prior to Baseline visit.
* Acetylcholine receptor autoantibody (anti-nAChR) titer or anti-AChR cluster antibody must be above the reference laboratory upper normal limit (UNL) and documented within the past 10 years of screening.
* Patient must be willing to return for all study visits.
* Patient must be able to give written informed consent.
* Women of childbearing potential must agree to use highly effective birth control from Screening until 14 days post last dose of Descartes-08,
Exclusion Criteria:
* Major chronic illness that is not well managed at the time of study entry and in the opinion of the investigator may increase the risk to the patient.
* Diagnosis of gMG within 12 months of screening.
* No history of systemic treatment for gMG other than acetylcholine esterase inhibitors.
* Diagnosis of a neuromuscular disease other than gMG.
* Patient is pregnant or lactating.
* Treatment with intravenous immunoglobulin (IVIG) or plasma exchange within 4 weeks prior to the Baseline visit.
* Treatment with rituximab or ocrelizumab within 12 months prior to Baseline visit; treatment with calcineurin inhibitors (e.g. tacrolimus, cyclosporine, cyclophosphamide), Neonatal Fc receptor antagonists, and/or other biologics within 3 weeks prior to planned leukapheresis and within 8 weeks prior to Baseline visit.
* The patient has started treatment with a complement 5a (C5a) inhibitor, such as eculizumab, within 8 weeks of Baseline visit. (NOTE: patients who have been receiving a C5a inhibitor for more than 8 weeks and meet other criteria for enrollment are eligible for treatment).
* Prior treatment with B-cell maturation antigen (BCMA)-directed therapy (e.g. monoclonal antibody, T-cell engager, or chimeric antigen receptor T-cell \[CAR-T\]).
* Abnormal prothrombin (PT)/international normalized ratio (INR) or partial thromboplastin time (PTT) increased \> 1.5-fold above the normal range at Screening or patient is on anticoagulation therapy (except in cases of elevated PTT with documented lupus anticoagulant; or in patients who have been on stable doses of anticoagulation therapy for more than 6 months of venous thromboembolism (VTE) diagnosis; or in patients on stable doses of anticoagulation therapy for at least 8 weeks of atrial fibrillation diagnosis; these conditions will not be exclusionary unless, in the investigator's opinion, they make participation in the study unsafe).
* Absolute neutrophil count (ANC) \< 1000 cells/microliter.
* Hemoglobin \< 8.0 g/dL.
* Platelets \< 50,000/mm3.
* Alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) \> 3x above normal.
* Creatine clearance less than 30 mL/min.
* History of primary immunodeficiency, organ, or allogeneic bone marrow transplant.
* Patients must be seronegative for hepatitis B surface antigen.
* Patients must be seronegative for hepatitis C antibody. If hepatitis C antibody test is positive, then patients must be tested for the presence of viremia by reverse transcriptase polymerase chain reaction (RT-PCR) and must be hepatitis C virus (HCV) ribonucleic acid (RNA) negative.
* History of positive human immunodeficiency virus (HIV) or positive HIV at screening.
* Active tuberculosis or positive QuantiFERON test at screening.
* Any other clinical or laboratory abnormality that, in the opinion of the investigator, may jeopardize the subject's ability to participate in the study or could affect study outcome.
* Any active significant cardiac or pulmonary disease that, in the opinion of the Principal Investigator, is significant and/or uncontrolled.
Note: Patients with asthma and chronic obstructive pulmonary disease (COPD) controlled with inhaled medications are allowed.
* History of malignancy that required treatment in the past 3 years, except for squamous cell carcinoma, basal cell carcinoma of the skin, or breast or early-stage colon cancer that is surgically removed and did not require adjuvant chemotherapy or radiotherapy.
* Treatment with any investigational agent 4 weeks prior to screening or 5 half-lives of the investigational drug (whichever is longer).
* Receipt of a live vaccination within 4 weeks prior to Baseline visit or intent to receive live vaccination during the study (Note: messenger RNA \[mRNA\]-based vaccines such as those against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are not considered live; likewise, the Janssen Covid-19 vaccine is not live).
* History of significant recurrent infections or any active infection that in the opinion of the Investigator may interfere with the patient's participation in the opinion of the investigator.
* Any known psychiatric illness that in the opinion of the Investigator, may interfere with the patient's participation in the study in the opinion of the investigator.
Primary outcome measure(s)
- Myasthenia Gravis Activities of Daily Living (MG-ADL) — assessment at 4 months of study
To evaluate the efficacy of Descartes-08 as assessed by the proportion of Myasthenia Gravis Activities of Daily Living (MG-ADL) responders at Month 4.
Trial sites (34)
| Facility | City | Region | Status |
| A40 |
Tucson |
Arizona |
|
| A13 |
Carlsbad |
California |
|
| A46 |
Los Angeles |
California |
|
| A14 |
Orange |
California |
|
| A21 |
Aurora |
Colorado |
|
| A50 |
Washington D.C. |
District of Columbia |
|
| A48 |
Maitland |
Florida |
|
| A10 |
Tampa |
Florida |
|
| A53 |
O'Fallon |
Illinois |
|
| A20 |
Fairway |
Kansas |
|
| A16 |
Lexington |
Kentucky |
|
| A38 |
Boston |
Massachusetts |
|
| A12 |
Amherst |
New York |
|
| A52 |
New York |
New York |
|
| A47 |
New York |
New York |
|
| A22 |
Chapel Hill |
North Carolina |
|
| A39 |
Charlotte |
North Carolina |
|
| A15 |
Portland |
Oregon |
|
| A11 |
Philadelphia |
Pennsylvania |
|
| A49 |
Pittsburgh |
Pennsylvania |
|
| A43 |
Houston |
Texas |
|
| A41 |
Seattle |
Washington |
|
| A54 |
Milwaukee |
Wisconsin |
|
| A18 |
Toronto |
Canada |
|
| A23 |
Rome |
Italy |
|
| A30 |
Krakow |
Poland |
|
| A24 |
Belgrade |
Serbia |
|
| A25 |
Barcelona |
Spain |
|
| A26 |
Barcelona |
Spain |
|
| A31 |
Madrid |
Spain |
|
| A32 |
Ankara |
Turkey (Türkiye) |
|
| A17 |
Istanbul |
Turkey (Türkiye) |
|
| A33 |
Birmingham |
United Kingdom |
|
| A51 |
Sheffield |
United Kingdom |
|