Phase 3 Efficacy Analysis of a Typhoid Conjugate Vaccine Trial in Nepal

N Engl J Med. 2019 Dec 5;381(23):2209-2218. doi: 10.1056/NEJMoa1905047.

Abstract

Background: Salmonella Typhi is a major cause of fever in children in low- and middle-income countries. A typhoid conjugate vaccine (TCV) that was recently prequalified by the World Health Organization was shown to be efficacious in a human challenge model, but data from efficacy trials in areas where typhoid is endemic are lacking.

Methods: In this phase 3, randomized, controlled trial in Lalitpur, Nepal, in which both the participants and observers were unaware of the trial-group assignments, we randomly assigned children who were between 9 months and 16 years of age, in a 1:1 ratio, to receive either a TCV or a capsular group A meningococcal conjugate vaccine (MenA) as a control. The primary outcome was typhoid fever confirmed by blood culture. We present the prespecified analysis of the primary and main secondary outcomes (including an immunogenicity subgroup); the 2-year trial follow-up is ongoing.

Results: A total of 10,005 participants received the TCV and 10,014 received the MenA vaccine. Blood culture-confirmed typhoid fever occurred in 7 participants who received TCV (79 cases per 100,000 person-years) and in 38 who received MenA vaccine (428 cases per 100,000 person-years) (vaccine efficacy, 81.6%; 95% confidence interval, 58.8 to 91.8; P<0.001). A total of 132 serious adverse events (61 in the TCV group and 71 in the MenA vaccine group) occurred in the first 6 months, and 1 event (pyrexia) was identified as being vaccine-related; the participant remained unaware of the trial-group assignment. Similar rates of adverse events were noted in the two trial groups; fever developed in 5.0% of participants in the TCV group and 5.4% in the MenA vaccine group in the first week after vaccination. In the immunogenicity subgroup, seroconversion (a Vi IgG level that at least quadrupled 28 days after vaccination) was 99% in the TCV group (677 of 683 participants) and 2% in the MenA vaccine group (8 of 380 participants).

Conclusions: A single dose of TCV was immunogenic and effective in reducing S. Typhi bacteremia in children 9 months to 16 years of age. (Funded by the Bill and Melinda Gates Foundation; Current Controlled Trials number, ISRCTN43385161.).

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Double-Blind Method
  • Endemic Diseases / prevention & control
  • Female
  • Humans
  • Incidence
  • Infant
  • Kaplan-Meier Estimate
  • Male
  • Meningococcal Vaccines / adverse effects
  • Meningococcal Vaccines / immunology
  • Nepal / epidemiology
  • Salmonella typhi / isolation & purification*
  • Typhoid Fever / diagnosis
  • Typhoid Fever / epidemiology
  • Typhoid Fever / prevention & control*
  • Typhoid-Paratyphoid Vaccines / adverse effects
  • Typhoid-Paratyphoid Vaccines / immunology*
  • Vaccines, Conjugate / adverse effects
  • Vaccines, Conjugate / immunology*

Substances

  • Meningococcal Vaccines
  • Typhoid-Paratyphoid Vaccines
  • Vaccines, Conjugate

Associated data

  • ISRCTN/ISRCTN43385161