PEG-rhG-CSF in Patients With Breast Cancer Receiving Chemotherapy to Prevent Neutropenia
NCT ID: NCT02805205
Last Updated: 2016-06-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
484 participants
INTERVENTIONAL
2013-04-30
2016-02-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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PEG-rhG-CSF
patients received a single dose of 100 ug/kg of PEG-rhG-CSF(pegfilgrastim), on the basis of actual body weight, as a single subcutaneous injection on day 3 after chemotherapy
PEG-rhG-CSF
Interventions
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PEG-rhG-CSF
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* diagnosis of breast cancer patients who need to receive multi-cycle chemotherapy
* grade III/IV neutropenia after chemotherapy
* KPS score≥70
* life expectancy of at least 3 months
* Written informed consent are acquired
Exclusion Criteria
* uncontrolled infection
* pregnancy
* Other situations that investigators consider as contra-indication for this study
18 Years
70 Years
ALL
No
Sponsors
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CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
INDUSTRY
Responsible Party
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Other Identifiers
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CSPC-PGC-IV-02
Identifier Type: -
Identifier Source: org_study_id
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