A Safety Study to Assess a DNA Vaccine Administered by Particle Mediated Delivery to the Skin in Healthy Subjects
Completed · Phase 1
Conditions studied: HSV-2
In brief
The purpose of this study is to evaluate how well the vaccine is tolerated at sites where administrations are given and any effects it may have on subjects' wellbeing. The study will also test the ability of vaccine to cause particular immune responses in the body.
Key facts
- Study ID
- NCT00310271
- Run by
- PowderMed
- People needed
- 42
- Starts
- 2006-04-01
- Expected to finish
- 2006-12-01
- Last updated by the study team
- 2008-11-21
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
Where it is running
- CPC Phase I Unit — Lenexa, Kansas, United States
Full record on ClinicalTrials.gov
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