Safety and Efficacy of ThisCART19 in Patients With Refractory or Relapsed B Cell Malignancies
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- STATUS
- Recruiting
-
- participants needed
- 30
-
- sponsor
- Fundamenta Therapeutics, Ltd.
Summary
This is a study to evaluate the safety and clinical activity of ThisCART19 (Allogeneic CAR-T targeting CD19) in patients with refractory or relapsed CD19 positive B cell malignancies.
Description
This is a single-center, nonrandomized, open-label study to evaluate the safety and clinical activity of ThisCART19 in patients with refractory or relapsed CD19 positive B cell malignancies, such as acute or chronic lymphocytic leukemia, lymphoma and etc. The dose range is 0.2-6 x 10^6 cells per kg body weight.
Details
Condition | B Cell Malignancy |
---|---|
Age | 3years - 70years |
Treatment | ThisCART19 cells |
Clinical Study Identifier | NCT04384393 |
Sponsor | Fundamenta Therapeutics, Ltd. |
Last Modified on | 19 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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