drugset / Trial / NCT03870945
Safety of MB-CART2019.1 in Lymphoma Patients (MB-CART2019.1 Lymphoma / DALY 1)
Non-randomizedSequentialOpen-labelTreatment
Summary
This is a prospective, multi-center, open phase I/II trial to evaluate feasibility, dosage, safety and toxicity as well as efficacy of ex vivo expanded autologous T cells genetically modified to express anti-CD20 and CD19 immunoreceptor (MBCART2019.1) in patients with relapsed or resistant aggressive CD20 and CD19 positive B-NHL/CLL/SLL.
Timeline
- Start
- 2019-02-25
- Primary completion
- 2020-12-17
- Completion
- 2024-05-28
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | zamtocabtagene autoleucel | Cell therapy | 1e+06 cells/kg | Intravenous |
| Subject | zamtocabtagene autoleucel | Cell therapy | 2.5e+06 cells/kg | Intravenous |