E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Vaccination against HZ and its related complications in adults older than 50 years (at the time of primary vaccination). |
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E.1.1.1 | Medical condition in easily understood language |
Herpes zoster (Shingles) disease. |
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E.1.1.2 | Therapeutic area | Diseases [C] - Virus Diseases [C02] |
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 19.1 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10019982 |
E.1.2 | Term | Herpes zoster NOS |
E.1.2 | System Organ Class | 100000004862 |
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E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
To assess the Vaccine Efficacy (VE) in the prevention of Herpes Zoster (HZ) over the total duration of the ZOSTER-049 (Z49) study overall as measured by the reduction in HZ risk in subjects ≥50 years of age at the time of first vaccination in the ZOSTER-006/022 (Z6/22) studies. |
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E.2.2 | Secondary objectives of the trial |
VE in HZ prevention in subjects of each age*: 1 During Z49 VE in HZ prevention in subjects ≥50Y & each age*: 2 From 1 month p-Dose2 in Z6/22 to Z49 end 3 Over each Y from 1 month p-Dose2 in Z6/22 VE in PHN prevention in subjects ≥50Y & each age*: 4 During Z49 5 From 1 month p-Dose2 in Z6/22 to Z49 end Immuno at Y 5, 6, 7, 8, 9 & 10 & beyond Z6/22 p-1’ vacc. in subjects ≥50Y & in each age*: 6 HI 7 CMI Immuno at Y 5, 6, 7, 8, 9 & 10 & beyond Z6/22 p-1’ vacc. in subjects ≥50Y with conf. HZ: 8 HI 9 CMI Immuno 1 month p-1st additional HZ/su dose (1AdD** & Rev & Ctrl): 10 HI 11 CMI Immuno 1 month p-2nd additional HZ/su dose (Rev & Ctrl): 12 HI 13 CMI Immuno at Y 1, 2, 3, 4, 5 & 6 of Z49 (1AdD, Rev & Ctrl): 14 HI 15 CMI 16 Safety & reacto (1AdD & Rev) 17 Safety (LTFU & Ctrl)
*Ages: 50-59, 60-69, ≥60 & ≥70Y at Day 1 in Z6/22. Y=year; p-=post; 1’=primary; HI=Humoral Immuno; CMI=Cell-Mediated Immuno. **Groups: 1AdD=1-Additional Dose; Rev=Revaccination; Ctrl=Control. |
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
•Subjects who, in the opinion of the investigator, can and will comply with the requirements of the protocol (e.g., completion of the diary cards, return for follow-up visits, ability to have scheduled contacts to allow evaluation during the study). Or subjects with a caregiver who, in the opinion of the investigator, can and will comply with the requirements of the protocol (e.g., completion of the diary cards, availability for follow-up contacts); •Written informed consent obtained from the subject prior to performance of any study specific procedure; •Subject who participated in ZOSTER-006 or ZOSTER-022 studies and received at least one dose of HZ/su vaccine.
Additional inclusion criteria for the 1-Additional Dose, Revaccination and Control groups, ONLY: •Female subjects of non-childbearing potential may be enrolled in this study. -Non-childbearing potential is defined as pre-menarche, current tubal ligation, hysterectomy, ovariectomy or post-menopause. •Female subjects of childbearing potential may be enrolled in this study, if the subject: -has practiced adequate contraception for 30 days prior to vaccination, and -has a negative pregnancy test on the day of vaccination and -has agreed to continue adequate contraception during the entire treatment period and for 2 months after com-pletion of the vaccination series. |
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E.4 | Principal exclusion criteria |
•Use of any investigational or non-registered product (pharmaceutical product or device) at the time of enrolment or planned use during the study period; •Previous vaccination against VZV or HZ and/or planned administration during the study of a VZV or HZ vaccine (including an investigational or non-registered vaccine other than the HZ/su vaccine administered in studies ZOSTER-006/022); •Chronic administration (defined as > 14 consecutive days in total) of immunosuppressants or other immune-modifying drugs during the period starting six months prior to Visit Month 0 of study ZOSTER-049 or expected administration at any time during the study period. For corticosteroids, this will mean prednisone ≥ 20 mg/day or equivalent. A prednisone dose of < 20 mg/day is allowed. Inhaled, topical and intra-articular corticosteroids are allowed; •Administration of long-acting immune-modifying drugs (e.g., infliximab, rituximab) within 6 months prior to Visit Month 0 of study ZOSTER-049 or expected administration at any time during the study period; •Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease (e.g., malignancy, human immunodeficiency virus [HIV] infection) or immunosuppressive/cytotoxic therapy (e.g., medications used during cancer chemotherapy, organ transplantation or to treat autoimmune disorders); •Administration of immunoglobulins and/or any blood products within 3 months prior to Visit Month 0 of study ZOSTER-049 or planned administration during the study period; •Prolonged use (> 14 consecutive days) of oral and/or par-enteral antiviral agents that are active against VZV (acyclovir, valacyclovir, famciclovir, etc. ) and planned to be used during the study period for an indication other than to treat suspected or confirmed HZ or an HZ-related complication (topical use of these antiviral agents is allowed). •Important underlying illness that in the opinion of the investigator would be expected to interfere significantly during the study;
Additional exclusion criteria for the 1-Additional Dose, Revaccination and Control groups, ONLY: •Subjects who experienced an SAE from first vaccination in the previous ZOSTER-006/022 studies to enrolment in study ZOSTER-049 that was considered related to study vaccine by either the investigator or the sponsor; •Subjects with a new onset of a pIMD or exacerbation of a pIMD from first vaccination in the previous ZOSTER-006/022 studies to enrolment in study ZOSTER-049; •Use of any investigational or non-registered product (pharmaceutical product or device) within 30 days preceding the first dose of study vaccine or planned use during the study period; •Administration or planned administration of any other immunizations within 30 days before the first study vaccination or scheduled within 30 days after study vaccination. However, licensed non-replicating vaccines (i.e., inactivated and subunit vaccines, including inactivated and subunit influenza vaccines for seasonal or pandemic flu, with or without adjuvant) may be administered up to 8 days prior to each dose and/or at least 14 days after any dose of study vaccine; •History of allergic disease or reactions likely to be exacerbated by any component of the vaccine. Additionally, consider allergic reactions to other material or equipment related to study participation (such as materials that may possibly contain latex -gloves, syringes, etc.). Please note, the vaccine and vials in this study do not contain latex; •Pregnant or lactating female; •Female planning to become pregnant or planning to discon-tinue contraceptive precautions (if of childbearing potential); •Previous episode/history of HZ. |
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E.5 End points |
E.5.1 | Primary end point(s) |
Confirmed HZ cases (LTFU and Control groups). |
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E.5.1.1 | Timepoint(s) of evaluation of this end point |
During the entire study period. |
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E.5.2 | Secondary end point(s) |
1. Confirmed HZ cases.
2. PHN cases.
3. Antigen-gE humoral immunogenicity (Anti-gE Ab concentrations as determined by ELISA).
4. CMI in terms of frequencies of antigen-specific CD4+ T cells (Frequencies of CD4+ T cells with antigen-specific Interferon gamma (IFN-γ) and/or Interleukin-2 (IL-2) and/or Tumour Ne-crosis Factor alpha (TNF-α) and/or CD40 Ligand (CD40L) secretion/expression to gE as determined by ICS).
5. Solicited local and general symptoms in subjects administered with 1 or 2 additional doses of HZ/su vaccine (1-Additional Dose and Revaccination groups).
6. Unsolicited AEs in subjects administered with 1 or 2 additional doses of HZ/su vaccine (1-Additional Dose and Revaccination groups).
7. Occurrence and relationship to vaccination of all SAEs (1-Additional Dose, Revaccination and Control groups).
8. Occurrence of SAEs related to investigational vaccine, related to study participation or to GSK concomitant medication/vaccine (All subjects).
9. Occurrence and relationship to vaccination of all AEs of specific interest: Potential immune-mediated diseases (pIMDs) (1-Additional Dose, Revaccination and Control groups). |
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E.5.2.1 | Timepoint(s) of evaluation of this end point |
1 and 2. 1 month post dose 2 in the previous Z-006/022 studies to study end.
3 and 4. At months 0, 12, 24, 36, 48, 60 and 72 (LTFU HI and CMI subsets, 1-Additional Dose, Revaccination and Control groups), and at Month 1 (1-Additional Dose, Revaccination and Control groups), and at Month 3 (Revaccination and Control groups).
5. 7 days (Days 0-6) after each vaccination.
6. 30 days (Days 0-29) after each vaccination.
7 and 9. From Month 0 to Month 12 (1-Additional Dose and Control groups) and from Month 0 until 12 months after last HZ/su vaccination (Revaccination group).
8. During the entire study. |
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | Yes |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | Yes |
E.6.13.1 | Other scope of the trial description |
reactogenicity, immunogenicity. |
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E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | No |
E.8.1.2 | Open | Yes |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | No |
E.8.1.5 | Parallel group | No |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | Yes |
E.8.1.7.1 | Other trial design description |
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E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | No |
E.8.2.3 | Other | Yes |
E.8.2.3.1 | Comparator description |
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E.8.2.4 | Number of treatment arms in the trial | 4 |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 99 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | No |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
Australia |
Brazil |
Canada |
Czech Republic |
Estonia |
Finland |
France |
Germany |
Hong Kong |
Italy |
Japan |
Korea, Republic of |
Mexico |
Spain |
Sweden |
Taiwan |
United Kingdom |
United States |
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E.8.7 | Trial has a data monitoring committee | No |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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Last Visit Last Subject or Last Contact Last Subject |
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 7 |
E.8.9.1 | In the Member State concerned months | 0 |
E.8.9.1 | In the Member State concerned days | 10 |
E.8.9.2 | In all countries concerned by the trial years | 7 |
E.8.9.2 | In all countries concerned by the trial months | 0 |
E.8.9.2 | In all countries concerned by the trial days | 10 |