Solid Organ Transplant SHINGRIX

Terminated

• Conditions: Kidney Transplant; Complications
• Interventions: Biological: SHINGRIX

• Registration Number: NCT03993717
• Lead Sponsor: Emory University

Brief Summary

This study will assess the immune responses to the recombinant, AS01-adjuvanted varicella zoster virus subunit (HZ/su) vaccine or SHINGRIX in immunosuppressed patients, particularly those who have received a renal transplant, and aim to better understand if the vaccine and perhaps other adjuvanted vaccines are safe in these patients.

30 participants will be divided into 2 groups, one group will receive the 1st out of 2 doses of the vaccine 3-6 months after transplant per standard of care and the second group will receive the 1st out of 2 doses of the vaccine 12-36 months after the transplant per standard of care.The duration of the study is 180 days.

Detailed Description

Shingles is a viral illness caused by the same virus that causes the chicken pox. Reactivation of this virus leads to shingles which is a painful blistering rash. Around 10% of organ transplant patients get shingles. This study will help us assess the safety and efficacy of a new shingles vaccine, SHINGRIX in Kidney Transplant patients. SHINGRIX is FDA approved for the prevention of shingles.

In this study, participants will be divided into 2 groups, one group will receive the 1st out of 2 doses of the vaccine 3-6 months after transplant per standard of care and the second group will receive the 1st out of 2 doses of the vaccine 12-36 months after the transplant per standard of care.

This research is conducted at the Emory University Hospital and Emory Clinics. Additionally follow up visits might also be conducted at the Emory Hope Clinic, the clinical arm of the Emory Vaccine Center.

Subjects will be identified through review of medical records or by referral from their healthcare providers. Subjects may also self-refer from the IRB approved recruitment flyers. Following identification/referral, a coordinator or recruiter will contact the subject and tell them about the study and see if he/she is interested. If the potential subject is interested, the recruiter will obtain an oral consent and prescreen them for the study using a screening checklist. Qualified subjects will be scheduled to come into the clinic and be fully consented and proceed with screening/enrollment.

Blood specimens will be collected and stored for the research study and for future use. Subjects can opt to have their information stored in a Hope Clinic database in order to contact them for other studies they may qualify for in the future. There are no other optional studies planned at this time.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2019-06-18
• Study First Submitted QC: 2019-06-20
• Study First Posted: 2019-06-21
• Study Start: 2020-01-30
• Primary Completion: 2020-08-08
• Study Completion: 2020-08-08
• Status Verified: 2024-02
• Last Update Submitted: 2024-02-15
• Last Update Posted: 2024-02-20

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 2

Inclusion Criteria

1. Capable of informed consent and provision of written informed consent before any study procedures.
2. Capable of attending study visits according to the study schedule
3. Males or females greater than or equal to 50 years of age.
4. Oral temperature less than 38 C.
5. Are in general good health, as determined by medical history and targeted physical exam related to this history
6. Recent renal transplant (either 3-6 months or 12-36 months prior)
7. Have received maintenance immunosuppressive therapy for prevention of allograft rejection for a minimum of 30 days prior to the first vaccination
8. Have received an ABO compatible allogeneic renal transplant
9. Male subjects should agree not to contribute to conception of a child, including sperm donation, for the duration of the study.

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Exclusion Criteria

1. Have received any transplant in addition to renal transplant
2. Have an acute illness within 72 hours prior to vaccination
3. Have a severe medical condition as determined by the investigators
4. Have kidney disease related to any known immune/autoimmune phenomena including, but not limited to: systemic lupus erythematosus, glomerulonephritis (post-streptococcal, Goodpasture syndrome, granulomatosis with polyangitis, polyarteritis nodosa, etc.).
5. Be on systemic immunosuppressive agents aside from those related to their renal transplant
6. Have known HIV or primary immune deficiency
7. Have a known potential immune-mediated disorder (pIMD)
8. Have planned receipt of any unlicensed or investigational medications, biologics, or vaccines for the duration of subject study participation
9. Have a history of severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine
10. Have donated blood or blood products within 56 days before study vaccination and for the duration of the study
11. Have received the Shingrix or Zostavax injection previously
12. Have had Shingles in the past
13. Be of child-bearing potential
14. Have known recent exposure to wild-type varicella in the past 4 weeks
15. Have a history of severe reactions following other vaccinations

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Three to six months post-transplant Group	SHINGRIX	Subjects in this arm will receive the SHINGRIX vaccine three to six months after kidney transplant
Twelve to thirty-six months post-transplant Group	SHINGRIX	Subjects in this arm will receive the SHINGRIX vaccine twelve to thirty-six months after kidney transplant

Primary Outcome Measures

Name	Time	Method
Change in levels of Anti-gE antibody concentrations	Day 1, Day 61, Day 180	Anti-gE antibody concentrations will be obtained via enzyme-linked immunosorbent assay (ELISA)
Change in number of subjects with a vaccine response for anti-gE antibody	Day 61, Day 180	Vaccine response is defined as: * For initially seronegative subjects, antibody concentration at post-vaccination greater than or equal to (≥) 4 fold the cut-off for Anti-gE (4x97 milli-international units per milliliter \[mIU/ml\]); * For initially seropositive subjects (defined as ≥ 97 mIU/ml), antibody concentration at post-vaccination ≥ 4 fold the pre-vaccination antibody concentration.

Secondary Outcome Measures

Name	Time	Method
Number of subjects with changes in allograft function	Day 180	Number of subjects with changes in allograft function from first vaccination until the end of the trial.; Allograft function will be defined as increase in serum creatinine levels (≥ 1.25, ≥ 1.50, ≥ 1.75 or ≥ 2 fold increase)
Number of subjects with any related severe adverse events (SAEs)	Day 180	Number of participants with SAEs from first vaccination until the end of the trial
Number of subjects with any grade 3 related adverse events (AEs)	Day 91	Number of subjects with any grade 3 related AEs from each vaccination and until 15 days after each vaccination
Number of subjects with renal allograft rejection	Day 180	Number of subjects with renal allograft rejection from first vaccination until the end of the trial
Change in HLA antibody titers	Day 1, Day 15, Day 61, Day 75, Day 180	HLA antibody titers will be measured and analyzed at different time points

Trial Locations

Locations (4)

Emory Clinic; 🇺🇸 Atlanta, Georgia, United States

Hope Clinic; 🇺🇸 Atlanta, Georgia, United States

Emory University Hospital; 🇺🇸 Atlanta, Georgia, United States

Emory University Hospital Clinical Research Network; 🇺🇸 Atlanta, Georgia, United States