drugset / Trial / NCT03016884

Safety and Tolerability of Herpes Zoster Vaccine Rheumatologic Patients

NCT03016884

Phase 4 Unknown 87 enrolled HaEmek Medical Center, Israel
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The reactivation of varicella zoster virus (VZV) (herpes zoster (HZ)) is of substantial public health concern. Updated ACR recommendations for RA treatment suggest that RA patients aged ≥ 50 years should be vaccinated before receiving biologic or tofacitinib therapy. The Investigators therefore propose a prospective study to evaluate the safety, tolerability, and immunogenicity of a zoster vaccine (Zostavax) in patients with RA, administered at least 2 weeks prior to initiation of anti-TNF biologic and tofacitinib therapy for RA. This is a 6-week open-label prospective multi-center study evaluating the safety, tolerability, and immunogenicity of Zostavax vaccine in the RA population prior to initiation of biologic/tofacitinib therapy for RA. VZV-specific immune response to vaccine in RA patients will be compared to healthy control subjects ≥ 50 years immunized with Zostavax.

Timeline

Start
2017-01
Primary completion
2019-09
Completion
2020-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Varivax Vaccine 19400 unknown Subcutaneous

Indications