The Treatment of Newly Diagnosed CD19+Mixed Phenotype Acute Leukemia in Adults
- Registration Number
- NCT06876701
- Lead Sponsor
- Ruijin Hospital
- Brief Summary
Evaluation the efficacy and safety of the combination of injectable bevacizumab, low-intensity chemotherapy, and venula in the treatment of newly diagnosed CD19+mixed phenotype acute leukemia in adults
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 10
- Patients fully understand this study, voluntarily participate and sign an informed consent form (ICF);
- Age: 18-75 years old (including boundary values of 18 and 75);
- Clinically diagnosed adult Mixed Phenotype Acute Leukemia (WHO 2016 criteria) patients with CD19 positivity
The subject's previous history of anti-tumor treatment meets one of the following conditions:
- Individuals who have previously received bevacizumab
- Individuals who have received CAR-T therapy or other gene modified cell therapies prior to screening;
- Within 5 half lives of the first use of the investigational drug, having received anti-tumor treatment including surgery, chemotherapy, targeted therapy, or participating in other clinical trials and receiving clinical trial medication;
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Experimental group Bevacizumab -
- Primary Outcome Measures
Name Time Method Negative conversion rate of evaluable residual lesions (MRD) 1 year
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Shanghai Zhaxin integrated hospital of traditional Chinese and Western Medicine
🇨🇳Shanghai, China