Last updated: 04/20/2021 12:10:08
Consistency, immunogenicity and safety study of GlaxoSmithKline (GSK) Biologicals’ Herpes Zoster (HZ) vaccine GSK1437173A in adults ≥ 50 years of age
EudraCT ID
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: Consistency, immunogenicity and safety study of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A in adults 50 years of age or older
Trial description: The purpose of this study is to demonstrate lot-to-lot consistency in terms of immunogenicity, and evaluate safety of the Herpes Zoster subunit (HZ/su) vaccine. The study is designed as a randomized, double-blind study with three parallel groups.
Primary purpose:
Prevention
Trial design:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Allocation:
Randomized
Primary outcomes:
Number of subjects with anti-gE antibody concentrations equal to or above the cut-off value
Timeframe: At Month 3
Secondary outcomes:
Anti-gE humoral immunogenicity
Timeframe: At Month 0 and Month 3
Number of vaccine responders for anti-gE concentrations as determined by ELISA
Timeframe: At Month 3
Number of subjects with any and Grade 3 solicited local symptoms
Timeframe: Within 7 days (Days 0-6) after each vaccine dose and across doses
Number of days with any solicited local symptoms
Timeframe: During the 7 days (Days 0-6) after each vaccine dose
Number of subjects with any, Grade 3 and related solicited general symptoms
Timeframe: Within 7 days (Days 0-6) after each vaccine dose and across doses
Number of days with any solicited general symptoms
Timeframe: During the 7 days (Days 0-6) after each vaccine dose
Number of subjects with any potential Immune-Mediated Diseases (pIMDs)
Timeframe: From first vaccination up to 30 days post last vaccination (Month 0-Month 3) and from Month 4 until study end (Month 14)
Number of subjects with any, Grade 3 and related unsolicited adverse events (AEs)
Timeframe: During 30 days (Days 0-29) after each vaccination
Number of subjects with any Serious Adverse Events (SAEs)
Timeframe: From first vaccination up to 30 days post last vaccination (Month 0-Month 3) and from Month 4 to study end (Month 14)
Interventions:
Biological/vaccine: Herpes Zoster vaccine (GSK 1437173A)
Enrollment:
651
Observational study model:
Not applicable
Primary completion date:
2015-29-04
Time perspective:
Not applicable
Clinical publications:
Strezova A et al. (2017) A randomized lot-to-lot immunogenicity consistency study of the candidate zoster vaccine HZ/su. Vaccine. 35(48 Pt B):6700-6706.
Medical condition
Herpes Zoster
Product
GSK1437173A
Collaborators
Not applicable
Study date(s)
August 2014 to April 2016
Type
Interventional
Phase
3
Participation criteria
Sex
Female & Male
Age
50+ years
Accepts healthy volunteers
Yes
- Subjects who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
- A male or female aged 50 years or older at the time of the first vaccination.
- Use of any investigational or non-registered product other than the study vaccine within 30 days preceding the first dose of study vaccine, or planned use during the study period.
- Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first vaccine dose. A prednisone dose of < 20 mg/day is allowed. Inhaled, topical and intra-articular corticosteroids are allowed.
Inclusion and exclusion criteria
Inclusion criteria:
- A male or female aged 50 years or older at the time of the first vaccination.
- Written informed consent obtained from the subject.
- Female subjects of non-childbearing potential may be enrolled in the study.
- Female subjects of childbearing potential may be enrolled in the 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 completion of the vaccination series.
Subjects who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
Non-childbearing potential is defined as pre-menarche, current tubal ligation, hysterectomy, ovariectomy or post-menopause.
Exclusion criteria:
- Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first vaccine dose. A prednisone dose of < 20 mg/day is allowed. Inhaled, topical and intra-articular corticosteroids are allowed.
- Administration or planned administration of a live vaccine in the period starting 30 days before the first dose of study vaccine and ending 30 days after the last dose of study vaccine, or, administration or planned administration of a non-replicating vaccine (E.g. inactivated and subunit vaccines) within 8 days prior to or within 14 days after either dose of study vaccine.
- Administration of long-acting immune-modifying drugs within six months prior to the first vaccine dose or expected administration at any time during the study period.
- Concurrently participating in another clinical study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product.
- Previous vaccination against HZ or varicella.
- Planned administration during the study of an HZ or varicella vaccine other than the study vaccine.
- History of HZ.
- Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease or immunosuppressive/cytotoxic therapy.
- History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccine.
- Acute disease and/or fever at the time of enrollment.
- Fever is defined as temperature ≥ 37.5°C (99.5°F) on oral, axillary or tympanic route, or ≥ 38.0°C (100.4°F) on rectal route. The preferred route for recording temperature in this study will be oral.
- Administration of immunoglobulins and/or any blood products within 3 months preceding the first dose of study vaccine or planned administration during the study period.
- Pregnant or lactating females.
- Females planning to become pregnant or planning to discontinue contraceptive precautions (if of childbearing potential) before Month 4.
- Any condition which, in the opinion of the investigator, prevents the subject from participating in the study.
- Any other condition that, in the opinion of the investigator, might interfere with the evaluations required by the study.
- Any condition which, in the judgment of the investigator would make intramuscular injection unsafe.
Use of any investigational or non-registered product other than the study vaccine within 30 days preceding the first dose of study vaccine, or planned use during the study period.
Subjects with a minor illness without fever may be enrolled at the discretion of the investigator.
Trial location(s)
Location
GSK Investigational Site
Coquitlam, British Columbia, Canada, V3K 3P4
Status
Study Complete
Location
GSK Investigational Site
Milford, Massachusetts, United States, 01757
Status
Study Complete
Study documents
Protocol
Available language(s): English
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Completed
Actual primary completion date
2015-29-04
Actual study completion date
2016-25-04
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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Additional information
IPD for this study will be made available via the Clinical Study Data Request site.
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