[A comparative study between different regimens for administering 2 doses of the Cuban anti-hepatitis B vaccine]

Rev Cubana Med Trop. 1998;50(3):218-20.
[Article in Spanish]

Abstract

A controlled clinical trial, corresponding to stage 2, was conducted in a population of sound adult males aged 18-23 to evaluate the immunogenicity of 5 schedules of Cuban vaccine against hepatitis B (Heberbiovac-HB [correction of Cheberbiovac-HB]). 5 groups were studied: I (control group 0, 1 and 6 months), II (0 and 2 months), III (0 and 4 months), IV (0 and 6 months), and V (0 and 8 months). The results showed no significant differences as regards the percentage of seroprotection of any of the groups of 2 doses compared with the control of 3 doses. It is concluded that between the first and the second dose there may be a period of time from 2 to 6 months with no need to reinitiate the schedule. This information will serve as a basis for a population based study to determine which schedule is the best to be used.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial
  • English Abstract

MeSH terms

  • Adolescent
  • Adult
  • Cuba
  • Dose-Response Relationship, Immunologic
  • Hepatitis B Antibodies / blood
  • Hepatitis B Vaccines / administration & dosage*
  • Hepatitis B Vaccines / immunology
  • Humans
  • Immunization Schedule
  • Male
  • Time Factors
  • Vaccines, DNA / administration & dosage*
  • Vaccines, DNA / immunology

Substances

  • Hepatitis B Antibodies
  • Hepatitis B Vaccines
  • Vaccines, DNA
  • heberbiovac-HB