Study to Evaluate the Impact of Reactogenicity on Quality of Life (QoL), After Administration of GlaxoSmithKline (GSK) Biologicals' Candidate Herpes Zoster Subunit (HZ/su) Vaccine (GSK1437173A) in Adults ≥ 50 Years of Age

Completed · Phase 3

Conditions studied: Herpes Zoster

In brief

The purpose of this study is to evaluate the impact of reactogenicity of GSK Biologicals' HZ/su vaccine on Quality of Life (QoL) in adults ≥ 50 years of age

Key facts

Study ID

NCT02979639

Run by

GlaxoSmithKline

People needed

404

Starts

2017-01-16

Expected to finish

2018-05-24

Last updated by the study team

2019-10-08

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects who, in the opinion of the investigator, can and will comply with the requirements of the protocol (e.g., completion of the questionnaires and diary cards).
• Written informed consent obtained from the subject prior to performance of any study specific procedure.
• A male or female aged ≥ 50 YOA at the time of consent.
• Female subjects of non-childbearing potential may be enrolled in the study.
• For this study population, non-childbearing potential is defined as current tubal ligation, hysterectomy, ovariectomy or post-menopause.
• 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.

You may not qualify if…

• Any condition which, in the judgment of the investigator, would make intramuscular (IM) injection unsafe.
• Use or planned use of any investigational or non-registered product (drug or vaccine) other than the study vaccine or current participation or planned concurrent participation in another clinical study, in which the subject has been or will be exposed to an investigational or a non-investigational product (pharmaceutical product or device) during the period starting 30 days before the first dose of study vaccine and the study end.
• Use or anticipated use of immunosuppressants or other immune-modifying drugs during the period starting 180 days prior to study start and during the whole study period. This includes chronic administration of corticosteroids (> 14 consecutive days of prednisone at a dose of ≥ 20 mg/day [or equivalent]), long-acting immune-modifying agents (e.g., infliximab) or immunosuppressive/cytotoxic therapy (e.g., medications used during cancer chemotherapy, organ transplantation or to treat autoimmune disorders). Inhaled, topical and intra-articular corticosteroids are allowed.
• 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 in the period starting 90 days preceding the first dose of study vaccine or planned administration during the study period.
• 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 in the period starting 15 days prior to and ending 14 days after either dose of study vaccine.
• Previous or planned administration of a vaccine against HZ (including an investigational or non-registered vaccine) other than the study vaccine, during the entire study period.
• History of HZ.
• History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccine.
• Female planning to become pregnant or planning to discontinue contraceptive precautions.
• Pregnant or lactating female.
• Significant underlying illness requiring medications that might confound the evaluation of general/ local AEs, or in the opinion of the investigator, would be expected to prevent completion of the study.
• Any other condition that, in the opinion of the investigator, might interfere with the evaluations required by the study.

Where it is running

• GSK Investigational Site — Oakland, California, United States
• GSK Investigational Site — Aurora, Colorado, United States
• GSK Investigational Site — Colorado Springs, Colorado, United States
• GSK Investigational Site — Colorado Springs, Colorado, United States
• GSK Investigational Site — Meridian, Idaho, United States
• GSK Investigational Site — Kansas City, Missouri, United States
• GSK Investigational Site — Durham, North Carolina, United States
• GSK Investigational Site — Corvallis, Oregon, United States
• GSK Investigational Site — Uniontown, Pennsylvania, United States
• GSK Investigational Site — Spartanburg, South Carolina, United States
• GSK Investigational Site — Norfolk, Virginia, United States

Full record on ClinicalTrials.gov

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