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Phase 3 N=1,000 Randomized Quadruple-blind Prevention

A Phase III Clinical Study to Evaluate SYN023's Efficacy and Safety

Rabies · Communicable Disease · Virus Diseases · Rhabdoviridae Infections · Mononegavirales Infections

Enrolled (actual)
1,000
Serious AEs
5.5%
Results posted
Apr 2023
Primary outcome: Primary: Rabies Virus Neutralizing Activity (RVNA) of Geometric Mean Concentration (GMC) at Study Day 8 — 4.346; 0.232 IU/mL

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
SYN023 (Biological); Human Rabies Immune Globulin (HRIG) (Biological); Rabies Vaccine (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Synermore Biologics (Suzhou) Co., Ltd.
Primary completion
Jun 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Rabies Virus Neutralizing Activity (RVNA) of Geometric Mean Concentration (GMC) at Study Day 8
4.346; 0.232
PRIMARY
Number of Probable or Confirmed Rabies Cases
0; 0
SECONDARY
Rabies Virus Neutralizing Activity (RVNA) of Geometric Mean Concentration (GMC)
4.212; 0.193; 13.590; 7.651; 13.084; 16.003
SECONDARY
Percentage of Participants With Rabies Virus Neutralizing Activity (RVNA) ≥0.5 IU/mL
99.8; 9.1; 99.6; 17.6; 100; 96.4
SECONDARY
Area Under the Efficacy Curve for the Geometric Mean Concentration (GMC) of Rabies Virus Neutralizing Activity (RVNA)
96.972; 31.869

Summary

This is a Phase 3, blinded, randomized study of SYN023 compared to a China licensed Human Rabies Immunoglobulin (a Rabies immune globulin from human sources, HRIG) for the prevention of rabies as part of post-exposure prophylaxis (PEP). The trial will enroll the World Health Organization (WHO) Category III rabies exposure subjects. The subject's death and rabies data will be reviewed by Data and safety monitoring board (DSMB) to confirm the safety. Besides, rabies vaccine would be administered after Study Drug in each group. This trial is proposed to further the licensure of SYN023 to provide an effective PEP alternative available to those exposed persons who need such a product. A placebo-controlled rabies trial is unethical thus HRIG is selected as the control group. Rabies immune globulin from equine and human sources (HRIG) have been evaluated in many trials and HRIG is the standard of care in China.

Eligibility Criteria

Inclusion Criteria

  • Is age ≥18 years, on Study Day 1 with legal identification documents, and plan to live in the local administration area during the study;
  • Category III rabies exposure within 24 hours before Study Drug receipt ;
  • Completed written informed consent process, and signed the informed consent forms;
  • Subjects with the ability to understand the study procedure. And agreed to complete all follow-ups;
  • Female subjects are not in pregnancy (with negative results of urine pregnancy tests before vaccination) and are not in the period of breast feeding, and agree to avoid pregnancy within 121 days after administration;
  • Those who have an armpit temperature ≤ 37.0 °C.

Exclusion Criteria

  • Previous receipt of equine or human (rabies) globulin or rabies vaccination prior to randomization;
  • Clinical evidence of rabies infection;
  • Category I and Category II rabies exposure;
  • Had fever (armpit temperature ≥ 38.5 °C) within 3 days before Study Day 1, or in the acute episode of any chronic diseases;
  • Received immunoglobulin or blood products (except for the anti-tetanus immunoglobulin) within 43 days before Study Day 1, or plan to use any such product (except for the anti-tetanus immunoglobulin) during the study;
  • Received systemic immunosuppressant medication such as systemic corticosteroids but not limited to systemic corticosteroids within 43 days before Study Day 1;
  • History of any immunodeficiency disease (for example: AIDS, systemic lupus erythematosus, etc.); or Laboratory evidence of previous or current immunodeficiency disease, including, but not limited to, any laboratory evidence of HIV infection;
  • History of spleen function deficiency or function injury, such as no spleen caused by any cause (such as splenectomy);
  • History of any severe allergy for vaccination, such as systemic urticaria, allergic laryngeal edema, anaphylactoid purpura, local allergic necrosis (Arthus reaction), angioedema, anaphylactic shock, etc., or allergic to any ingredient of the study drug/vaccine;
  • Previous receipt of any study product (drug, vaccine, biological product or medical device) within 6 months before Study Day 1, or plan to participate in any other clinical study during this study period;
  • History of or clinical evidence of any systemic disease, acute disease or chronic disease (such as convulsions, epilepsy, encephalopathy, nephrotic syndrome, etc.) that the investigator considers to be likely to interfere with safety or efficacy assessment of the study;
  • Previous medical history that may compromise the safety of the subject in the study according to the opinion of the principal investigator.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04644484). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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