Status:
UNKNOWN
Evaluate the Efficacy and Safety of the Prophylactic Use of PEG-rhG-CSF in Children With Hematological Malignancies
Lead Sponsor:
CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
Collaborating Sponsors:
Children's Hospital of Fudan University
Conditions:
Lymphoma
Leukemia
Eligibility:
All Genders
Up to 18 years
Phase:
NA
Brief Summary
The incidence of infectious complications in hematological malignancies is higher than that in children with solid tumors, which may be related to the type and dose intensity of chemotherapy regimens ...
Eligibility Criteria
Inclusion
- Under the age of 18, no gender limit;
- Children with hematological malignancies, leukemia or lymphoma, diagnosed by bone marrow pathology or cytology;
- The prophylactic use of PEG-rhG-CSF or rhG-CSF after chemotherapy is intended to prevent neutropenia, and the chemotherapy regimen must meet the interval between two chemotherapy sessions at least 12 days;
- The effect of chemotherapy in leukemia patients was complete remission, while that in lymphoma patients was complete remission or partial remission;
- The expected survival time is more than 8 months;
- Liver and kidney function: Liver function: total bilirubin (TBIL), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 times the upper limit of normal value, or≤5 times the upper limit of normal value when there is liver metastasis; renal function test: serum creatinine (Cr) ≤ 1.5 times the upper limit of normal value;
- Eastern Cooperative Oncology Group(ECOG) performance status(PS) \<2;
- The subjects had good mental consciousness, and the subject's legal guardian must sign an informed consent form;
- Researchers believe that the subject can benefit;
Exclusion
- Severe internal organ dysfunction;
- Those who used other test drugs of the same kind or accepted other clinical trials within 4 weeks before enrollment;
- Allergy to PEG-rhG-CSF, rhG-CSF and other preparations or proteins expressed by Escherichia coli;
- Researchers determine unsuited to participate in this trial.
Key Trial Info
Start Date :
August 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2021
Estimated Enrollment :
139 Patients enrolled
Trial Details
Trial ID
NCT04497701
Start Date
August 1 2020
End Date
December 1 2021
Last Update
August 4 2020
Active Locations (1)
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1
Children's Hospital of Fudan University
Shanghai, China