← Eichor
Study identifier: NCT07236814 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Suraxavir Marboxil And Oseltamivir for Influenza Prophylaxis Under a Hospital-based Setting

Condition: Influenza  ·  Sponsor: Capital Medical University

PhasePhase 3
Planned participants384
Who can joinAll sexes, 12 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to evaluate the efficacy of antiviral prophylaxis in preventing in-hospital influenza transmission. We will enroll hospitalized patients with confirmed influenza (index cases) and their uninfected roommates (room contacts). These room contacts will be randomized in a 1:1:1 ratio to one of three prophylactic groups: placebo, suraxavir marboxil, or oseltamivir. The primary outcome will be the rate of influenza infection among the room contacts, which will be monitored to determine the effectiveness of the interventions.

This description comes directly from the study's public registry record.

Talk to the study team

Yeming Wang, Ph.D.  ·  +86 84206264  ·  wwyymm_love@163.com

Always discuss trial participation with your own doctor first.

Locations (2)

China-Japan Friendship hospital, Beijing, BeijingBeijing, Beijing Municipality, ChinaNot Yet Recruiting
China-Japan Friendship HospitalBeijing, Beijing Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07236814