drugset / Trial / NCT01002040
Rapid Evaluation of Pandemic H1N1 Influenza Vaccine in Adults With HIV
Phase 4
Completed
150 enrolled
University of British Columbia
Canadian Institutes of Health Research (CIHR) · collabGlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelPrevention
Summary
The purpose of this study is to assess the safety and effectiveness (immune response) to a licensed H1N12009 influenza vaccine in HIV-infected adults. The study will enroll 150 adults (ages 20-59 years). Participants will be randomized into 2 groups and will receive either one dose or two doses of a licensed H1N1 vaccine. Study procedures include: medical history, blood samples and completing a memory aid. Participants will be involved in study related procedures for approximately 6 days.
Timeline
- Start
- 2010-02
- Primary completion
- 2010-07
- Completion
- 2010-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Arepanrix | Vaccine | — | — |