drugset / Trial / NCT01543087

Duration of hSBA Response After a Primary Series of Bivalent rLP2086 Followed by a Booster Dose

NCT01543087

Phase 3 Completed 698 enrolled Pfizer
Open-labelOther

Summary

This study is to assess the longevity of immune response in adolescents for approximately 48 months after receipt of a primary series of bivalent rLP2086 vaccination, which is then followed by a booster dose and an assessment of immune response for 12 or 26 months post booster vaccination.

Timeline

Start
2012-09-07
Primary completion
2018-01-05
Completion
2018-01-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Bivalent rLP2086 Vaccine