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Clinical Trials associated with pERIG FavirabVerorab® Immunogenicity and Safety After a One-week, 4-site, Intradermal (ID) Post-exposure Prophylaxis Regimen (4-4-4-0-0) Followed by a One-visit, 4-site, ID Booster at Five Years
The purpose of this study is to assess the 4-site "one-week" post-exposure prophylaxis (PEP) regimen as a possible alternative to the 2-site updated Thai Red Cross (TRC) PEP regimen.
Primary objective:
To demonstrate that PEP using the new "one-week, 4-site" (4-4-4-0-0) intradermal (ID) vaccination regimen is non-inferior to PEP using the updated TRC (2-2-2-0-2) ID vaccination regimen.
Secondary objectives:
Primary immunization: To describe the immune response in each group at Day 0, Day 14 and Day 90.
Antibody persistence: To describe rabies virus-neutralizing antibody persistence during the 5 years after completion of PEP in each group.
Booster vaccination: To describe the immune response induced by a single-visit 4-site intradermal booster vaccination in each group at Year 5.
Safety: To describe the safety profile of each group after the primary and booster vaccinations.
100 Clinical Results associated with pERIG Favirab
100 Translational Medicine associated with pERIG Favirab
100 Patents (Medical) associated with pERIG Favirab
100 Deals associated with pERIG Favirab