A Phase 1, Double-blinded, Placebo-Controlled Clinical Trial to Evaluate the Safety and Immunogenicity of HEV-239 (Hecolin(R)) Vaccine in Healthy US Adults
Mar-24
Journal Article
Authors:
            
  
    Kao, C. M.; 
          
  
    Rostad, C. A.; 
          
  
    Nolan, L. E.; 
          
  
    Peters, E.; 
          
  
    Kleinhenz, J.; 
          
  
    Sherman, J. D.; 
          
  
    Tippett, A.; 
          
  
    Shih, J. W. K.; 
          
  
    Yildirim, I.; 
          
  
    Agbakoba, V.; 
          
  
    Beresnev, T. ; 
          
  
    Ballou, C.; 
          
  
    Kamidani, S.; 
          
  
    Karmali, V.; 
          
  
    Natrajan, M.; 
          
  
    Scherer, E. M.; 
          
  
    Rouphael, N.; 
          
  
    Anderson, E. J.
  
Journal:
            J Infect Dis
      
PMID:
38536442
URL:
            https://www.ncbi.nlm.nih.gov/pubmed/38536442
      
Keywords:
      
              Hepatitis E acute hepatitis immunization
          
  
Abstract:
            <p>INTRODUCTION: Establishing the safety and immunogenicity of a hepatitis E virus vaccine in multiple populations could facilitate broader access and prevent maternal and infant mortality. METHODS: We conducted a phase 1, randomized, double-blinded, placebo-controlled (4:1 vaccine: placebo) trial of 30 microg HEV-239 (Hecolin(R), Xiamen Innovax Biotech Company Limited, China) administered intramuscularly in healthy US adults aged 18-45 years. Participants were vaccinated on days 1, 29, and 180. Participants reported solicited local and systemic reactions for 7 days following vaccination and were followed through 12 months after enrollment for safety and immunogenicity (IgG, IgM). RESULTS: Solicited local and systemic reactions between treatment and placebo group were similar and overall mild. No participants experienced serious adverse events related to HEV-239. All participants receiving HEV-239 seroconverted at one month following the first dose and remained seropositive throughout the study. HEV-239 elicited a robust hepatitis E IgG response that peaked one month following the second dose (Geometric Mean Concentration (GMC) 6.16; 95% CI 4.40-8.63), was boosted with the third dose (GMC 11.50; 95% CI 7.90-16.75) and persisted through 6 months. CONCLUSIONS: HEV-239 is safe and elicits a durable immune response through at least 6 months after the third dose in healthy US adults. CLINICAL TRIALS REGISTRATION: NCT03827395. Safety Study of Hepatitis E Vaccine (HEV239) - Full Text View - ClinicalTrials.gov.</p>