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Herpes Zoster clinical trials

View clinical trials related to Herpes Zoster.

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NCT ID: NCT00802464 Completed - Herpes Zoster Clinical Trials

Immunogenicity and Safety Study of GSK Biologicals' Herpes Zoster Vaccine With Various Formulations in Adults >= 50 Years

Start date: January 12, 2009
Phase: Phase 2
Study type: Interventional

The goal of this randomized observer-blind trial is to further refine the formulation of vaccines containing GSK1437173A in older adults by comparing the cellular and humoral immune responses and the safety profiles of the different formulations.

NCT ID: NCT00792623 Completed - Varicella Clinical Trials

Immunogenicity and Safety of GSK Biologicals' Live Attenuated Varicella Vaccine (VARILRIXTM).

Start date: September 8, 2003
Phase: Phase 2
Study type: Interventional

This study aims to assess the immunogenicity and safety of varicella vaccination in a population of autologous peripheral stem cell/ bone marrow transplantation recipients who have reached at least four months post-transplantation.

NCT ID: NCT00751348 Completed - Measles Clinical Trials

Immunogenicity & Safety Study of GSK Biologicals' Combined Measles-mumps-rubella-varicella Vaccine 208136

Start date: October 1, 2008
Phase: Phase 3
Study type: Interventional

This Phase 3b study is being conducted for the purpose of registration of the GSK208136 vaccine in Korea.

NCT ID: NCT00696709 Completed - Herpes Zoster Clinical Trials

A Study to Test the Safety and Antibody Response of V212 in Healthy Adults (V212-004)(COMPLETED)

Start date: December 12, 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study was to assess the safety and tolerability of gamma-irradiated varicella-zoster virus (VZV) vaccine A (Part 1) and gamma-irradiated VZV vaccine B and C (Part 2) and to determine if they were immunogenic when administered to healthy individuals, as measured by VZV-specific antibody responses by glycoprotein enzyme-linked immunosorbent assay (gpELISA). The primary hypothesis was that gamma-irradiated VZV vaccine A (Part 1) and gamma-irradiated VZV vaccine B and C (Part 2) would elicit an acceptable VZV-specific immune response. The secondary hypothesis for Part 1 of the study was that heat-treated VZV vaccine would elicit an acceptable VZV-specific immune response.

NCT ID: NCT00689013 Completed - Herpes Zoster Clinical Trials

The Effect of Pharmacist Intervention on the Use of Zostavax in a Community Pharmacy Setting

Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether pharmacist-driven patient interventions can have an effect on the number of herpes zoster (Zostavax) vaccinations given in a community pharmacy setting.

NCT ID: NCT00681031 Completed - Herpes Zoster Clinical Trials

Zostavax® at Minimum Release Specification Approaching Expiry (V211-044)

Start date: May 14, 2008
Phase: Phase 4
Study type: Interventional

Primary objective: To demonstrate whether or not ZOSTAVAX® at minimum release specification approaching expiry potency elicits an acceptable Varicella-Zoster Virus (VZV) antibody fold rise (measured by glycoprotein Enzyme Linked ImmunoSorbent Assay [gpELISA]) from pre-vaccination to 4 weeks post-vaccination. Secondary objectives: To describe the safety profile of ZOSTAVAX® at minimum release specification approaching expiry potency.

NCT ID: NCT00679796 Completed - Chickenpox Vaccines Clinical Trials

The Effectiveness of Varicella Vaccination in Children in Germany

Start date: February 2008
Phase: N/A
Study type: Observational

This study is undertaken to evaluate the effectiveness of currently licensed varicella vaccines under conditions of routine use in a setting where varicella vaccine is included in the childhood immunization calendar.

NCT ID: NCT00642785 Completed - Herpes Zoster Clinical Trials

Activation of Alternative Cellular Energy (ACE) Pathway in the Therapy of Herpes Virus Infections

Start date: January 2008
Phase: N/A
Study type: Observational

The research question to be addressed is whether indirect phototherapy based activation of the body's alternative cellular energy (ACE) pathway will lead to expedited healing of active herpes simplex virus (HSV) and herpes zoster virus (HZV)skin lesions, and also possibly inhibit both latent HSV infections and residual HZV infections.

NCT ID: NCT00578175 Completed - Measles Clinical Trials

Immunogenicity and Safety of GlaxoSmithKline Biologicals' MMRV Vaccine vs. ProQuad® in Children 12-14 Months of Age

Start date: November 20, 2007
Phase: Phase 2
Study type: Interventional

The purpose of this observer blinded study is to provide information on vaccine immunogenicity and reactogenicity in comparison with the US standard of care (ProQuad®) when administered with Hepatitis A vaccine and Pneumococcal vaccine.

NCT ID: NCT00576108 Completed - Neuropathic Pain Clinical Trials

A 2 Week Study of Topical KD7040 in the Treatment of Postherpetic Neuralgia (PHN)

Start date: November 2007
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety and efficacy of 2 weeks of topical KD7040 versus placebo in the treatment of postherpetic neuralgia.