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Herpes Zoster clinical trials

View clinical trials related to Herpes Zoster.

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NCT ID: NCT01165203 Completed - Herpes Zoster Clinical Trials

Study to Evaluate GSK Biologicals' Herpes Zoster Vaccine GSK1437173A in Human Immunodeficiency Virus (HIV)-Infected Subjects

Start date: September 30, 2010
Phase: Phase 2
Study type: Interventional

This observer-blind study will evaluate the safety and immunogenicity of GlaxoSmithKline (GSK) Biologicals' investigational Herpes Zoster (HZ) vaccine GSK1437173A in Human Immunodeficiency Virus (HIV) infected subjects, firstly enrolling subjects treated with antiretroviral therapy (ART) and with high CD4 T cell counts, and subsequently ART-treated subjects with low CD4 T cell counts, and ART-naïve subjects with high CD4 T cell counts. This Protocol Posting has been updated following Amendment 1 of the Protocol, August 2010. The impacted sections is exclusion criteria.

NCT ID: NCT01165177 Completed - Herpes Zoster Clinical Trials

Study to Evaluate Efficacy, Safety and Immunogenicity of GSK Biologicals' Herpes Zoster (HZ) Vaccine GSK1437173A in Adults Aged 50 Years and Older

Start date: August 2, 2010
Phase: Phase 3
Study type: Interventional

The purpose of this observer-blind study is to evaluate the efficacy, safety and immunogenicity of GSK Biologicals' candidate Herpes Zoster (HZ) vaccine in adults aged ≥ 50 years. Two studies [ZOSTER-006 (NCT01165177) and ZOSTER-022 (NCT01165229)] are being conducted concurrently to evaluate efficacy of GSK1437173A vaccine. A pooled analysis of data from both studies combined will be conducted contingent on each study achieving its objectives. The protocol posting of study ZOSTER-022 also deals with the outcome measures related to the pooled analysis.

NCT ID: NCT01160081 Completed - Hepatitis A Clinical Trials

Seroprevalence Study of Hepatitis A, Varicella-Zoster, Cytomegalovirus, Herpes Simplex and Bordetella Pertussis

Start date: March 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine the seroprevalence of Hepatitis A Virus (HAV), Varicella-Zoster virus (VZV), Cytomegalovirus (CMV), Herpes Simplex (HSV) and Bordetella pertussis (BP)infections in Mexico.

NCT ID: NCT01138215 Completed - HIV Infections Clinical Trials

The Immunogenicity of Varicella-zoster Virus Vaccine in HIV-infected Children

Start date: June 2009
Phase: Phase 4
Study type: Interventional

To study about the immunogenicity, safety and efficacy of varicella-zoster virus vaccine in HIV-infected children.

NCT ID: NCT01137669 Completed - Herpes Zoster Clinical Trials

ZOSTAVAX® in Renal Transplant Patients

Start date: September 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety of a licensed zoster vaccine, ZOSTAVAX® (Zoster Vaccine Live) in 40 subjects, age 18 years or older, with chronic kidney disease (CKD) who are scheduled to receive a living donor kidney transplant. ZOSTAVAX® is not licensed for use in immunosuppressed persons and in the United States for individuals less than 50 years of age. Subjects will receive either ZOSTAVAX® vaccine or placebo (inactive substance) no less than 4 weeks prior to their kidney transplant. Study procedures include: physical exam, blood samples and documentation of daily temperatures and/or side effects in a diary following vaccination. Participants may be involved in study related procedures for up to 18 months.

NCT ID: NCT01132729 Completed - Herpes Zoster Clinical Trials

Bioequivalency Study of Valacyclovir Hydrochloride 1000 mg Under Fasting Conditions

Start date: September 2006
Phase: N/A
Study type: Interventional

The objective of this study was to prove the bioequivalence of Valacyclovir Hydrochlorothiazide Caplet under fasting conditions.

NCT ID: NCT01132716 Completed - Herpes Zoster Clinical Trials

Bioequivalency Study of Valacyclovir Hydrochloride 1000 mg Under Fed Conditions

Start date: September 2006
Phase: N/A
Study type: Interventional

The objective of this study was to prove the bioequivalence of Valacyclovir Hydrochlorothiazide Caplet under fed conditions.

NCT ID: NCT01086449 Completed - Herpes Zoster Clinical Trials

Safety and Immunogenicity of GSK Biologicals' Herpes Zoster Vaccine 1437173A in Healthy Ethnic Japanese Adults

Start date: March 4, 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety, reactogenicity and immunogenicity of GSK Biologicals' candidate Herpes Zoster (HZ) vaccine in healthy ethnic Japanese adults.

NCT ID: NCT01077804 Completed - Herpes Zoster Clinical Trials

A Study to Evaluate Long-term Impact of VARIVAX Among Children and Adolescents (V210-036)(COMPLETED)

Start date: June 1995
Phase: N/A
Study type: Observational

The purpose of these continuing post-licensure studies is to evaluate the long-term effectiveness of VARIVAX® [Varicella Virus Vaccine Live (Oka/Merck)] and to assess the impact of the vaccine on the epidemiology of varicella and herpes zoster.

NCT ID: NCT00986232 Completed - Measles Clinical Trials

ProQuad Dose Selection Study (V221-011)(COMPLETED)

Start date: April 1999
Phase: Phase 2
Study type: Interventional

A Study comparing three different doses of ProQuad to concomitant administration of M-M-R II and PUVV (Process Upgrade Varicella Vaccine) vaccines.