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Efficacy and Cost Benefit in Filgrastim Biosimilar for Neutropenia in Patients Receiving Chemotherapy: A Single-center, Non-randomized Cohort Study

Efficacy and Cost Benefit in Filgrastim Biosimilar for Neutropenia in Patients Receiving Chemotherapy: A Single-center, Non-randomized Cohort Study - Efficacy of Filgrastim Biosimilar

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019110
Enrollment
20
Registered
2015-09-24
Start date
2014-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Gynecologic cancer

Interventions

Injection method Chemotherapy cycle 1 When febrile neutropenia [fever (axillary temperature with less than neutrophil count 1,000/mm3 more than 38 degrees Celsius)] develops at chemotherapy enforcem

Sponsors

Oita University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Enforcement planned Patient Performance status(PS)is the patient with hematopoiesis, liver, the renal function to meet criteria of Patient following with 0-1 by the pharmacotherapy in the anticancer drug Neutrophile count>1,500/mm3 Platelet>100,000/mm3 1.5 times of 1.5 times serum creatinine <institution reference value upper limit of 2.5 times total bilirubin<institution reference value upper limit of GOT and GPT <institution reference value upper limit

Exclusion criteria

Exclusion criteria: 1) The patients with the bone marrow infiltration 2) Is the patients with hypersensitivity to Patient 3) G-CSF preparation which received radiotherapy within four weeks before registration at chemotherapy initiation 4) The patients who judged that a chief physician was inappropriate

Design outcomes

Primary

MeasureTime frame
Neutropenic (neutrophil count <1,000/mm3) period in each treatment cycle

Countries

Japan

Contacts

Public ContactYuhki Sato

Oita University Hospitaly Clinical Pharmacy

syuhki@oita-u.ac.jp097-586-6101

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026