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Influenza, Human clinical trials

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NCT ID: NCT00633074 Completed - Influenza Clinical Trials

Non-inferiority Study of GSK Biologicals' Influenza Vaccine GSK576389A Using Different Formulations

Start date: March 3, 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to show the non-inferiority of different formulations of GlaxoSmithKline Biologicials' influenza vaccine.

NCT ID: NCT00630331 Completed - Influenza Clinical Trials

Efficacy Study of Two Influenza Vaccines and Placebo in Healthy Adult Subjects

Start date: October 2007
Phase: Phase 3
Study type: Interventional

The present study will evaluate clinical efficacy, safety, tolerability and immunogenicity of both Novartis Vaccines' cell-derived influenza vaccine and egg-derived influenza vaccine in healthy adults 18 to 49 years of age.

NCT ID: NCT00620815 Completed - Influenza Clinical Trials

Safety and Immunogenicity of Two Doses of a Tetravalent Influenza Vaccine in Adults Aged 18 Years and Above

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

Evaluate the immune response and reactogenicity of H5N1 vaccination in adults aged 18 years and above (as part of a tetravalent vaccine)

NCT ID: NCT00617851 Completed - Influenza Clinical Trials

Study to Evaluate the Consistency of Three Consecutive Production Lots of Influenza Vaccine in Healthy Subjects 18 to 49 Years Old

Start date: November 2007
Phase: Phase 3
Study type: Interventional

The purpose of this research is to demonstrate immunologic equivalence of three consecutive production lots of the subunit influenza vaccine compared to egg-derived inactivated influenza vaccine in healthy subjects 18 to 49 years of ages. In addition, this study is to show how safe and well tolerated a conventional inactivated subunit influenza vaccine, licensed in many countries outside the United States, is compared to an inactivated influenza vaccine, licensed in the United States.

NCT ID: NCT00617331 Completed - Influenza Clinical Trials

H9 Priming Study in Healthy Adults

Start date: February 2008
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to determine whether prior exposure to A/H2N2 viruses is associated with better antibody (part of the immune system that fights infection) responses after vaccination with an A/H9N2 flu vaccine. The study will evaluate how much antibody is made to the influenza virus after H9N2 flu vaccination and how the body reacts to different strengths of the H9N2 flu vaccine. This information may guide vaccine development for this virus as well as other bird flu viruses that have infected humans. Study participants will include 120 healthy subjects, age 18-38 or 44-59 years. Two different dosages of vaccine will be given in the muscle of the upper arm about 1 month apart. The assignment of vaccines to participants is governed by chance. Study procedures may include medical history, physical exam, and blood samples. Study participation duration is about 7 months.

NCT ID: NCT00617318 Completed - Influenza Clinical Trials

Pomegranate Products for Prevention of Common Cold

Start date: January 2007
Phase: Phase 3
Study type: Interventional

Pomegranate has a long history of use in folk medicine. There is vast data on the health benefits of pomegranate fruit and juice. Multiple studies have established the strong antioxidative effects of pomegranate polyphenols (primarily the ellagitannin punicalagin) and their health effects. A vast number of animal and human clinical studies have provided evidence on effect of pomegranate products on improving blood lipid profile, reducing blood pressure, improving endothelial function, anti-tumor activity, and its anti-atherosclerotic activity. We studied the protective effect of a pomegranate concentrate (POM Flu and Cold Formula®) in decreasing the incidence and duration of influenza-like illnesses and common cold among healthy adults.

NCT ID: NCT00616928 Completed - Influenza Clinical Trials

Immunogenicity & Safety of GSK's Influenza Vaccine 1557484A Given to Adults Aged ≥18 Years

Start date: January 23, 2008
Phase: Phase 3
Study type: Interventional

The purpose of this Phase 3, observer-blind, placebo-controlled, multi-center study is to characterize the immunogenicity & safety of the investigation vaccination regimen of GSK 1557484A vaccine given to adults aged ≥18 years.

NCT ID: NCT00606359 Completed - Influenza Clinical Trials

Immunogenicity of the Inactivated Split-Virion Influenza Vaccine in Renal Transplant Subjects

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

Primary Objective: To describe the immunogenicity of an injection of the investigational inactivated, split-virion influenza vaccine 21 days after vaccination in 18 to 60 years old renal transplant subjects identified as non-responder to previous vaccination with the IM reference vaccine (Vaxigrip®). Secondary Objective: To describe the safety of an injection of the investigational inactivated, split-virion influenza vaccine in 18 to 60 years old renal transplant subjects identified as non-responder to previous vaccination with the IM reference vaccine

NCT ID: NCT00603811 Completed - Influenza Infection Clinical Trials

Phase I Safety and Immunogenicity Study of VAX102 [Flagellin.HuM2e] Influenza Vaccine in Healthy Adults

Start date: September 2007
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety and immunogenicity of VAX102 [Flagellin.HuM2e], a recombinant, inactivated, subunit influenza vaccine given as a two dose regimen at a range of doses.

NCT ID: NCT00593970 Completed - Pregnancy Clinical Trials

Influenza Vaccine in Pregnancy Part 2

Start date: November 2007
Phase:
Study type: Observational

Pregnant women have limited knowledge regarding influenza, its implications during pregnancy, and recommendations for vaccination during pregnancy. The researchers plan to distribute an information pamphlet to women in a prenatal clinic, offer the vaccine during prenatal visits, and then give a questionnaire on the postpartum floor assessing knowledge. The researchers hypothesize that with education intervention, knowledge scores on the questionnaire will be higher than those from last year, when no education was provided.