About this trial
This study is a prospective single-arm open-labled phase I/II clinical trial, including dose escalation and expansion phase, aims to evaluate the safety, efficacy, and cellular pharmacokinetics of GT719 Injection in relapsed/refractory CD19 positive adult B-cell non Hodgkin lymphoma (B-NHL) and B-acute lymphoblastic leukemia (B-ALL) patients. A total of 46 subjects (anticipated) will be enrolled in this study.
Eligibility criteria
Qualifiers
Voluntarily enrolled in the study, signed an informed consent form, and willing and able to comply with the study protocol.
Eastern Collaborative Oncology Group (ECOG) physical fitness status score of 0 or 1.
CD19 positivity confirmed by flow cytometry and/or histopathology.
Disqualifiers
Primary immunodeficiency.
History of symptomatic deep vein thrombosis or pulmonary embolism within 6 months prior to enrollment, requiring systemic anticoagulant therapy.
Any medical condition that may interfere with the evaluation of the safety or effectiveness of research and treatment;
Trial design
Treatments tested in this trial
- GT719 Injection
Treatment groups
Sponsors and collaborators
Grit Biotechnology
Lead sponsor
Institute of Hematology & Blood Diseases Hospital, China
Collaborator