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The Treatment of Newly Diagnosed CD19+Mixed Phenotype Acute Leukemia in Adults

Early Phase 1
Not yet recruiting
Conditions
Acute Leukemia
Interventions
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
Inclusion Criteria
  1. Patients fully understand this study, voluntarily participate and sign an informed consent form (ICF);
  2. Age: 18-75 years old (including boundary values of 18 and 75);
  3. Clinically diagnosed adult Mixed Phenotype Acute Leukemia (WHO 2016 criteria) patients with CD19 positivity
Exclusion Criteria

The subject's previous history of anti-tumor treatment meets one of the following conditions:

  1. Individuals who have previously received bevacizumab
  2. Individuals who have received CAR-T therapy or other gene modified cell therapies prior to screening;
  3. 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
GroupInterventionDescription
Experimental groupBevacizumab-
Primary Outcome Measures
NameTimeMethod
Negative conversion rate of evaluable residual lesions (MRD)1 year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Shanghai Zhaxin integrated hospital of traditional Chinese and Western Medicine

🇨🇳

Shanghai, China

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