Clinical Trial

Boostability Assessment of Three Rabies Pre-Exposure Regimens in Healthy Volunteers 5 Years Following Priming.

Study acronym: BAZOOKA_221
Not Yet Recruiting Phase 3
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Summary
A multicentre, open label trial in healthy volunteers to assess the boostability of three different rabies pre-exposure prophylaxis regimens (2 x 1IM regimen, 2 x 2 ID regimen, 1 x 2 ID regimen) when administering a single-dose, intramuscular vaccination as simulated post-exposure prophylaxis at least five years following priming.
Trial Details
NCT Number NCT07455318
Lead Sponsor Institute of Tropical Medicine, Belgium
Conditions Rabies (Healthy Volunteers)
Enrollment 561 participants
Start Date 2026-05-15
Primary Completion 2027-06 (estimated)
Study Completion 2027-06 (estimated)
Updated on ClinicalTrials.gov 2026-03-06