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A Study to Evaluate the Safety, Reactogenicity and Immunogenicity of Ad26.ZIKV.001 in Healthy Adult Volunteers

NCT03356561 PHASE1 COMPLETED

The purpose of this study is to assess the safety, reactogenicity, and immunogenicity of Ad26.ZIKV.001 at 2 dose levels, 5\*10\^10 viral particles (vp) and 1\*10\^11 vp, administered intramuscularly as single dose and as 2-dose schedules in healthy adults.

Details

Lead sponsorJanssen Vaccines & Prevention B.V.
PhasePHASE1
StatusCOMPLETED
Enrolment100
Start dateSun Nov 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionMon Sep 23 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

United States