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Garenoxacin to Prevent Febrile Neutropenia in Chemotherapy for Lung Cancer

Garenoxacin to Prevent Febrile Neutropenia in Chemotherapy for Lung Cancer - Garenoxacin to Prevent Febrile Neutropenia in Chemotherapy for Lung Cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014711
Enrollment
30
Registered
2014-07-30
Start date
2010-12-01
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

Lung cancer

Interventions

In lung cancer patients who had febrile neutropenia in the privious chemotherapy, garenoxacin is prescribed in the next cycle of chemotherapy from day 8 for 1 week or until grade 2 neutropenia to prev

Sponsors

Institute of Biomedical Research and Innovation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients with lung cancer during chemotherapy 2)Patients who experienced febrile neutropenia 3)Dose of chemotherapy is not changed in the next cycle of the therapy. 4)Age: over 20 5)Adequate organ functions judged by laboratory tests. 6)Life expectancy: longer than 3 months 7)Wrtten informed consent

Exclusion criteria

Exclusion criteria: 1)Tumor fever 2)Complication such as severe infection or comobidities 3)History of severe allergic reaction 4)History of epilepsy or convulsant 5)Clinically significant heart disease 6)Uncontrolled diabetes 7)Routine use of NSAIDS 8)Routine use of steroids or immuno-suppressant 9)Chronic aspiration 10)Clinically significant psychological problems 11)unsuitable patients whom physitians consider

Design outcomes

Primary

MeasureTime frame
The incidence of clinically documented febrile episode

Secondary

MeasureTime frame
The incidence of all probable infections The site of infection Pathogenic bacteria The incidence of death Safety

Countries

Japan

Contacts

Public ContactAkito Hata

Institute of Biomedical Research and Innovation Division of Integrated Oncology

a-hata@fbri.org078-304-5200

Outcome results

None listed

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