The purpose of the trail is to evaluate the efficacy and safety of PEG-rhG-CSF in primary
prophylaxis and secondary prophylaxis of neutropenia after chemotherapy.
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT02905916
Ages eligible for Study
18 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
Patients with age between 18 and 70 years.
Breast cancer, lymphoma, bone tumor or Gynecologic tumor patients.
With multi-cycle chemotherapy.
With III/IV degree neutropenia after the last cycle of chemotherapy and plans to use the same regimen in the subsequent cycles.FN risk of the chemotherapy regimens is
≥20%，or 10%≤FN risk＜20% and has high risk factors associated with FN.
KPS score≥ 70.
Expected to survive more than 3 months.
No hematologic system disease and ANC≥1.5×10E9/L, PKT≥80×10E9/L, Hb≥ 75g/L, WBC≥3×10E9/L, and no bleeding tendency.
Written informed consent are acquired. -
With infection or systemic antibiotic therapy 72h before chemotherapy.
With any abnormal hematopoietic function.
Received transplantation within 3 months.
Suffered from other malignant tumor or brain metastases.
TBIL, ALT,AST > 2.5×ULN; if it were caused by liver metastases, TBIL, ALT,AST >5×ULN.
Cr >1.5 ×ULN.
Sensitive to the product or other genetically engineered biological products from Escherichia coli strains.
Mental or nervous system disorders.
Refused to accept contraceptive measures.
Other situations that investigators consider as contra-indication for this study.
All locations for NCT02905916
Peking University Cancer Hospital
Beijing, China, 100142
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View full eligibility
Tris trial is registered with FDA with number: NCT02905916. The sponsor of the trial is Peking University and it is looking for 217 volunteers for the current phase.
Official trial title:
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