Last reviewed · How we verify
Safety and Immunogenicity of Recombinant Zoster Vaccine for Transplant Recipients (SIR ZOSTER)
The goal of this clinical trial is to compare responses to Varicella Zoster vaccination between transplant patients on different medication regimens, and their healthy co-habitants. The main questions it aims to answer are: 1. Are there differences in vaccination immunological responses in transplant patients on different immunosuppression regimens? 2. Are there differences in vaccination immunological responses between transplant patients and their healthy co-habitants? Participants will all receive a 2-dose course of SHINGRIX recombinant Zoster vaccination, and have immunological responses measured and compared at 5 timepoints between 1 week to 1 year post-vaccination.
Details
| Lead sponsor | Central Adelaide Local Health Network Incorporated |
|---|---|
| Phase | NA |
| Status | RECRUITING |
| Enrolment | 160 |
| Start date | 2024-03-20 |
| Completion | 2027-12 |
Conditions
- Immunosuppression
- Vaccine Response Impaired
Interventions
- Recombinant zoster vaccine adjuvanted (SHINGRIX)
Primary outcomes
- Functional T cell memory — 3 weeks following second vaccine dose
ELISpot measurement of interferon gamma spot-forming units following 18-hour stimulation of peripheral blood mononuclear cells with Zoster gE protein-derived peptide array
Countries
Australia