Cross-vaccination Study of GSK Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine (GSK 1437173A) in Subjects Who Previously Received Placebo in ZOSTER-006 (NCT01165177) and ZOSTER-022 (NCT01165229) Studies.

Completed · Phase 3

Conditions studied: Herpes Zoster

In brief

The purpose of this study is to cross-vaccinate and collect safety data in terms of unsolicited Adverse Events (AEs), Serious Adverse Events (SAEs) and potential Immune Mediated Disease (pIMD) from subjects \>= 50 Years of age (YOA) who previously received placebo in ZOSTER-006 (NCT01165177) and ZOSTER-022 (NCT01165229).

Key facts

Study ID: NCT02690207
Run by: GlaxoSmithKline
People needed: 8687
Starts: 2016-03-16
Expected to finish: 2019-03-15
Last updated by the study team: 2021-03-04

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 diary cards, vaccination visits, follow-up contacts). Or subjects' Legally Acceptable Representative(s) [LAR(s)]/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, vaccination visits, availability for follow-up contacts).
Written informed consent obtained from the subject/Legally Acceptable representative(s) [LAR(s)] of the subject prior to performing any study specific procedure. If the subjects is not capable of giving consent, his/her assent to participate should be obtained to the extent possible.
Subject who previously participated in ZOSTER-006 or ZOSTER-022 studies and received at least one dose of placebo.
Female subjects of non-childbearing potential may be enrolled in the 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 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.
treatment period refers to vaccination days and the interval between them.

You may not qualify if…

Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine during the period starting 30 days before the first dose of study vaccine (Day -29 to Day 0), or planned use up to 30 days post Dose 2.
Previous vaccination against Varicella Zoster virus (VZV) or HZ.
Planned administration of VZV or HZ vaccination during the study (including an investigational or non-registered vaccine), with the exception of the study vaccine.
Planned administration/administration of a vaccine/product not foreseen by the study protocol in the period starting 30 days before the first dose and ending 30 days after the last dose of vaccine administration, with the exception of licensed non-replicating vaccines (i.e. inactivated and subunit vaccines, including inactivated and subunit influenza vaccines, with or without adjuvant for seasonal or pandemic flus). These may be administered up to 8 days prior to dose 1 and/or dose 2 and/or at least 14 days after any dose of study vaccine
Chronic administration (defined as more than 14 days in total) of immunosuppressants or other immune-modifying drugs during the period starting six months prior to the first vaccine dose and up to 30 days post Dose 2. For corticosteroids, this will mean prednisone ≥ 20 mg/day or equivalent. Inhaled, topical and intra-articular corticosteroids are allowed.
Administration of long-acting immune-modifying drugs (e.g. infliximab, rituximab) within six months prior to the first vaccine dose up to 30 days post Dose 2.
Concurrently participating in another clinical study, at the time of enrolment or planned participation up to the 30 days post second dose, in which the subject has been or will be exposed to an investigational or a non-investigational vaccine/product (pharmaceutical product or device).
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).
History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccine.
Active HZ infection at the time of enrolment (i.e. HZ lesions not completely crusted over).
Pregnant or lactating female.
Any condition which, in the opinion of the investigator, prevents the subject from participating in the study.
Any condition which in the judgment of the investigator would make intramuscular injection unsafe.

Where it is running

GSK Investigational Site — Phoenix, Arizona, United States
GSK Investigational Site — Phoenix, Arizona, United States
GSK Investigational Site — Phoenix, Arizona, United States
GSK Investigational Site — Tucson, Arizona, United States
GSK Investigational Site — Spring Valley, California, United States
GSK Investigational Site — Clearwater, Florida, United States
GSK Investigational Site — DeLand, Florida, United States
GSK Investigational Site — Jacksonville, Florida, United States
GSK Investigational Site — Jacksonville, Florida, United States
GSK Investigational Site — West Palm Beach, Florida, United States
GSK Investigational Site — Meridian, Idaho, United States
GSK Investigational Site — Wichita, Kansas, United States
GSK Investigational Site — Columbia, Maryland, United States
GSK Investigational Site — Elkridge, Maryland, United States
GSK Investigational Site — Kansas City, Missouri, United States
GSK Investigational Site — Las Vegas, Nevada, United States
GSK Investigational Site — Somers Point, New Jersey, United States
GSK Investigational Site — Cary, North Carolina, United States
GSK Investigational Site — Charlotte, North Carolina, United States
GSK Investigational Site — Hickory, North Carolina, United States
GSK Investigational Site — Salisbury, North Carolina, United States
GSK Investigational Site — Wilmington, North Carolina, United States
GSK Investigational Site — Winston-Salem, North Carolina, United States
GSK Investigational Site — Cleveland, Ohio, United States
GSK Investigational Site — Mesa, Arizona, United States

Full record on ClinicalTrials.gov

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