CompletedPhase 2NCT02005458
Safety and Efficacy of YPEG-rhG-CSF in Cancer Patients Receiving Chemotherapy
Studying Small cell lung cancer
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Xiamen Amoytop Biotech Co., Ltd.
- Principal Investigator
- Yuankai Shi, Ph.DCancer Institute and Hospital, Chinese Academy of Medical Sciences
- Intervention
- YPEG-rhG-CSF, 20μg/kg, single s.c. at 48hrs after chemotherapy for each experimental cycle(drug)
- Enrollment
- 80 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2013 – 2018
Study locations (12)
- Zhangzhou Municipal Hospital of Fujian Province, Zhangzhou, Fujian, China
- Shaaxi Provincial Tumor Hospital, Xi'an, Shaanxi, China
- Cancer Institute and Hospital, CAMS, Beijing, China
- Fujian cancer hospital, Fuzhou, China
- Fujian Medical University Union Hospital, Fuzhou, China
- Fuzhou General Hospital of Nanjing Military Command, Fuzhou, China
- The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- Shanghai Changzheng Hospital, Shanghai, China
- Shanghai Chest Hospital, Shanghai, China
- Tongji Hospital, Tongji Medical College Huazhou University of Science & Technology, Wuhan, China
- The First Affiliated Hospital of Xiamen University, Xiamen, China
- Zhejiang cancer hospital, Zhejiang, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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