Skip to content

Fetroja for Intravenous Drip Infusion Regular Drug Use-results Survey

Fetroja for Intravenous Drip Infusion Regular Drug Use-results Survey - Fetroja for Intravenous Drip Infusion Regular Drug Use-results Survey

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000053151
Enrollment
200
Registered
2023-12-19
Start date
2023-12-20
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

Infections

Interventions

None listed

Sponsors

Shionogi & Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: NA

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Incidence proportions of adverse drug reactions including Safety specification items of Fetroja for Intravenous Drip Infusion

Secondary

MeasureTime frame
Clinical effectiveness and bacteriological examinations by bacterial species and infectious disease

Countries

Japan

Contacts

Public ContactHaruna Hayashi

SHIONOGI & Co., Ltd. Pharmacovigilance Department

haruna.hayashi@shionogi.co.jp+81-6-6209-6923

Outcome results

None listed

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