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Prevention and treatment of neutropenia associated with antineoplastic therapy: a real-world study

Prevention and treatment of neutropenia associated with antineoplastic therapy: a real-world study

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021713
Enrollment
Unknown
Registered
2019-03-06
Start date
2019-03-04
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Interventions

Case series:Mecapegfigrastim injection

Sponsors

Shandong Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Patients with clinically diagnosed non-myeloid malignant tumors; 2) Patients receiving treatment regimens that are susceptible to granulocytopenia; 3) Subjects joined the study voluntarily, signed the informed consent, and cooperated with the follow-up. 4) Women of childbearing age must have pregnancy test (serum) within 7 days before admission, and the results are negative. They are willing to use appropriate contraceptive methods during the trial and within 8 weeks after the last administration of the test drug. 5) ECOG PS 0-2.

Exclusion criteria

Exclusion criteria: 1) Pregnant or lactating women; 2) Patients with primary bone tumors and medullary malignant tumors; 3) The patients had other hematological diseases affecting the hematopoietic function of bone marrow; 4) People allergic to biological agents that study drugs or other G-CSF products or the expression of Escherichia coli; 5) According to the judgement of the researcher, the subjects have the accompanying diseases which seriously endanger the safety of the patients or affect the completion of the study; 5) The concomitant diseases that seriously endanger patients'safety or affect patients' completion of the study were judged by the researchers; 6) Other situations that are not suitable for inclusion in this study; 7) Patients who are participating in other clinical trials are not eligible to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Routine blood test;

Countries

China

Contacts

Public ContactLiu Bo

Shandong Cancer Hospital

tianfurong123456@163.com+86 15553115688

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026