Clinical Trials Directory

Trials / Unknown

UnknownNCT03493776

Safety and Immunogenicity of Non-live, Recombinant Subunit Herpes Zoster Vaccine Before and After Lung Transplantation

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Deepali Kumar · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

The investigators plan to study the immunogenicity of the vaccine before and after lung transplantation. Patients (at least 50 years old) before and after lung transplantation will be enrolled. The investigators hypothesize that the recombinant varicella-zoster subunit vaccine is able to induce cellular immunogenicity after transplantation.

Detailed description

Solid organ transplant recipients receive lifelong immunosuppression and are at increased risk for reactivation of all herpesviruses including VZV. Epidemiologic studies show the cumulative incidence in lung transplant recipients of reactivation to be 15-20%. A non-live, recombinant subunit vaccine (Shingrix; GSK vaccines) was recently licensed for the prevention of shingles in people aged 50 years or older. The investigators plan to study the immunogenicity of the vaccine before and after lung transplantation. Patients (at least 50 years old) before and after lung transplantation will be enrolled. The investigators hypothesize that the recombinant varicella-zoster subunit vaccine is able to induce cellular immunogenicity after transplantation.

Conditions

Interventions

TypeNameDescription
BIOLOGICALVZV subunit vaccineVZV subunit vaccine

Timeline

Start date
2018-04-15
Primary completion
2019-09-05
Completion
2021-04-01
First posted
2018-04-10
Last updated
2020-10-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03493776. Inclusion in this directory is not an endorsement.