drugset / Trial / NCT01460719

A Study to Evaluate the Safety and Immunogenicity of Inactivated Varicella-Zoster Virus (VZV) Vaccine in Adults With Hematologic Malignancies (HM) Receiving Treatment With Anti-Cluster of Differentiation (CD) 20 Monoclonal Antibodies (V212-013)

NCT01460719

Phase 1 Completed 80 enrolled Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelPrevention

Summary

An open-label, multicenter study to evaluate the safety and immunogenicity of inactivated VZV vaccine (V212) in participants with hematologic malignancies (HM) who are currently receiving anti-CD20 monoclonal antibodies. The primary hypothesis is that vaccination with V212 vaccine will elicit significant VZV-specific immune responses at \~28 days after vaccination 4. The statistical criterion for significance requires that the lower bound of the 2-sided 90% confidence interval of the geometric mean fold rise in immune response in V212 recipients is \>1.0.

Timeline

Start
2012-01-24
Primary completion
2012-09-25
Completion
2012-09-25

Drugs

EvaluationDrugModalityDoseRoute
Subject V212 Vaccine 0.5 ml Subcutaneous

Indications