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A recombinant subunit vaccine used for active immunization against hepatitis B virus (HBV) infection. The vaccine is composed of the hepatitis B surface antigen (HBsAg), which is produced using recombinant DNA technology in yeast cells. It works by stimulating the immune system to produce specific antibodies (anti-HBs) that provide protection against all known subtypes of HBV. This specific entry is associated with a Phase 4 clinical trial conducted by the Pontificia Universidad Catolica de Chile, which evaluates the serological response to an accelerated vaccination schedule (doses at 0, 1, and 2 months) in Haitian immigrants residing in Chile, a population identified as having a high prevalence of HBV exposure.
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