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Randomized study comparing Baloxavir Marboxil to Peramivir in pediatric patients with Influenza

Randomized study comparing Baloxavir Marboxil to Peramivir in pediatric patients with Influenza

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1051180014
Enrollment
40
Registered
2018-12-17
Start date
2018-12-12
Completion date
Unknown
Last updated
2025-07-18

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

Conditions

Influenza Influenza

Interventions

Interventions 1 Baloxavir marboxil Interventions 2 Peramivir

Sponsors

Kato Kentaro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)axillary temperature more than 37.5 degree 2)a positive rapid antigen test for influenza virus 3)a symptom duraiton of no more than 36 hours 4)hospitalized patient 5)body weight more than 10kg

Exclusion criteria

Exclusion criteria: 1)patients who have suffered from bacterial infection or other viral infection within one week from the start of the study 2)patients who received recipes of Baloxavir marboxil, Oseltamivir, Zanavivir, Laninavir, Peramivir within 4 weeks from the start of the study

Design outcomes

Primary

MeasureTime frame
The time to alleviation of influenza symptoms The time to resolution of fever

Secondary

MeasureTime frame
The changes from baseline in infectious virus and viral RNA titers

Contacts

Public ContactKentaro Kato

Kitano Hospital, Tazuke Kofukai Medical Research Institute

kenkato100@gmail.com+81-6-6312-1221

Outcome results

None listed

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