Real World Evidence Study of SYN023 in Children Exposed to Rabies

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-17
SponsorSynermore Biologics (Suzhou) Co., Ltd.

About this trial

This observational study is an open-label, prospective, multi-center design. The goal is to evaluate the long-term clinical survival outcomes at 3 months and 1 year in individuals under 18 years of age with WHO Category III rabies exposure who have received real-world Post-Exposure Prophylaxis (PEP) with Zamerovimab and Mazorelvimab Injection / other passive immunization products combined with the rabies vaccine.

Participants will: (1) Have their clinical protection outcomes (rabies-free survival status) registered and evaluated on Day 90 and Day 365. (2) Have the option to provide a blood sample on Day 7 for Rabies Virus Neutralizing Antibody (RVNA) testing. (3) Have all adverse events (within 42 days) and all serious adverse events (within 126 days) after PEP administration collected and recorded.

Eligibility criteria

Qualifiers

Age under 18 years on the day of enrollment, regardless of gender, and able to provide legal proof of identity;

Individuals with WHO Category III rabies exposure, and the time from exposure to the initiation of Post-Exposure Prophylaxis (PEP) is <7 days;

Have completed standardized wound management, injection of Zamerovimab and Mazorelvimab Injection /other passive immunization products, and the first dose of rabies vaccination within 24 hours prior to screening;

The volunteer's guardian voluntarily agrees to their participation in the study and signs the informed consent form. Specifically: for volunteers under 8 years old, the guardian signs the informed consent form with the child's assent fully respected; for volunteers aged 8-17, the guardian signs the informed consent form, and the minor volunteer signs the minor assent form;

Disqualifiers

Based on inquiry, besides the current Category III rabies exposure, there is a history of bites by dogs, cats, mongooses, foxes, ferrets, skunks, bats, or raccoons within the past year;

Other conditions considered by the investigator as unsuitable for participation in this study.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

232 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Synermore Biologics (Suzhou) Co., Ltd.

Lead sponsor

Peking University First Hospital

Collaborator

Shenzhen Second People's Hospital

Collaborator

Hunan Provincial People's Hospital

Collaborator

The University of Hong Kong-Shenzhen Hospital

Collaborator

University of South China Affiliated Nanhua Hospital

Collaborator