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Clinical Trials in China / NCT06876701
Starting soon Phase EARLY_PHASE1

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

NCT06876701 · tracked via the Priya Life Science China tracker
Sponsor
Ruijin Hospital
Phase
Phase EARLY_PHASE1
Started
2025-04-01
Last updated
2025-03-14

Condition(s) studied

Acute Leukemia

Investigational drug(s) / intervention(s)

Bevacizumab

Bevacizumab: Evaluation of 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

Study 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

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
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;

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Zhaxin integrated hospital of traditional Chinese and Western Medicine Shanghai China

On this site

📄 Avastin (bevacizumab) drug profile →

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06876701 on ClinicalTrials.gov ↗ ← All trials in China