Descartes-15 for Pts w/Relap/Refr MultipleMyeloma
Study Description
This is a Phase I dose-escalation study to evaluate the safety, tolerability and preliminary efficacy of an autologous BCMA-targeting RNA-engineered CAR T-cell therapy in patients with Relapsed/Refractory Multiple Myeloma. The cell product is referred to as Descartes-15
Eligibility
-Patients must be diagnosed with active and measurable relapsed/refractory multiple myeloma.
-Patients must have failed at least 3 prior lines of therapy which must have included an immunomodulatory drug, a proteasome inhibitor, and an anti-CD38 drug or biologic.
-Patients must have clinical performance status of ECOG 0-2.
-Patients must have adequate vital organ function as defined by:
-Patient must have labs drawn
-Normal cardiac and pulmonary function
-No thromboembolic events in the past 3 months
-No heparin allergy or active infection
-Patients who have any active and uncontrolled infection.
-Ongoing treatment with chronic immunosuppressants (e.g., cyclosporine or systemic steroids above 40 mg/day prednisone equivalent).
-Patients who have active central nervous system disease.
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