Drug intelligence / Profile preview

tetravalent dengue vaccine (purified inactivated)

Development stage
Discontinued
Lead developer
Walter Reed Army Institute of Research
Modality
Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

The tetravalent dengue purified inactivated vaccine (DPIV, also known as TDENV-PIV) is an investigational, formalin-inactivated whole-virus vaccine containing purified dengue virus types 1–4 (DENV-1 to DENV-4) propagated in Vero cells. Developed through a collaboration between the Walter Reed Army Institute of Research (WRAIR), GlaxoSmithKline (GSK), and Fiocruz, the vaccine was designed to prevent dengue fever by inducing neutralizing antibody responses against all four dengue virus serotypes. In clinical trials, formulations were evaluated with various adjuvants, including aluminum hydroxide (alum), AS01E, and AS03B, administered intramuscularly on a two-dose schedule. Although the vaccine demonstrated acceptable safety and induced robust peak neutralizing antibody titers, these responses waned relatively quickly, particularly in dengue-naive individuals. R&D has been discontinued, and no active clinical development is currently ongoing.

Other names
tetravalent dengue purified inactivated vaccinetetravalent dengue virus purified inactivated vaccine

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