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Healthy Adult Volunteers clinical trials

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NCT ID: NCT01354379 Completed - Clinical trials for Healthy Adult Volunteers

Safety and Immunogenicity Study of Inactivated Nasal Influenza Vaccine NB-1008 Administered by Sprayer

Start date: May 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety and immune response of a new intranasal vaccine against influenza, called NB-1008. The vaccine is composed of a licensed vaccine that is normally given as an injection, called Fluzone, and an adjuvant (additive that helps a vaccine work better), called W805EC. In a prior clinical study this vaccine showed promising results in terms of being well tolerated and eliciting mucosal and systemic immune responses after administration by a dropper. In this study NB-1008 is being administered by dropper as well as a nasal sprayer to determine if the sprayer further enhances the immune response.

NCT ID: NCT01333462 Completed - Clinical trials for Healthy Adult Volunteers

Safety and Immunogenicity Study of Inactivated Nasal Influenza Vaccine NB-1008

Start date: March 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety and immune response of a new intranasal vaccine against influenza, called NB-1008. The vaccine is composed of a licensed vaccine that is normally given as an injection, called Fluzone, and an adjuvant (additive that helps a vaccine work better), called W805EC.

NCT ID: NCT01129466 Completed - Clinical trials for Healthy Adult Volunteers

Effects of 2 Different Broccoli Sprout Containing Supplements on Nasal Cells in Healthy Volunteers

Broccosprout
Start date: May 2010
Phase: N/A
Study type: Interventional

Purpose: To compare the change in nasal cell HO-1 expression induced by two different preparations of sulforaphane (SFN)-containing nutritional supplements Participants: Healthy nonsmoking young adults, age 18-35 Procedures (methods): This pilot study will use a randomized crossover design. Subjects will be randomized to receive either the equivalent of 4 ounces/day of fresh broccoli sprouts (FBS) in food and tea, or the equivalent amount as broccoli sprout homogenates (BSH), for 3 consecutive days. Nasal lavage and blood samples will be obtained before, during and after this 3-day period. After at least a 2-week washout interval, the protocol will be repeated with the alternate supplement. The primary analysis will test the hypothesis that broccoli sprouts in food will increase HO-1 expression to a similar degree as the equivalent amount of sprouts in BSH

NCT ID: NCT01094834 Completed - Clinical trials for Healthy Adult Volunteers

A Multiple Dose Study of DWP05195 in Healthy Adult Subjects

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

The purpose of this study is to evaluate safety, tolerability, pharmacokinetics and pharmacodynamics of multiple administered DWP05195 in healthy volunteers