Trials / Completed
CompletedNCT01147068
Safety and Immunogenicity of PanBlok Influenza Vaccine in Healthy Adults
A Two-Part Placebo-Controlled Evaluation of the Safety and Immunogenicity of an A/Indonesia/5/05 Recombinant Hemagglutinin Influenza H5N1 Vaccine With and Without Glucopyranosyl Lipid A (GLA-SE) in Healthy Adults 18-49
- Status
- Completed
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 392 (actual)
- Sponsor
- Protein Sciences Corporation · Industry
- Sex
- All
- Age
- 18 Years – 49 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to investigate the safety and immunogenicity of a recombinant hemagglutinin (rHA) influenza vaccine derived from A/Indonesia/05/2005 (H5N1) administered at 4 dose levels in adjuvanted (GLA-SE) rHA formulations and 2 dose levels in unadjuvanted rHA formulations.
Detailed description
All currently licensed influenza vaccines in the United States are produced in embryonated hen's eggs. There are several well-recognized disadvantages to the use of eggs as the substrate for influenza vaccine. Eggs require specialized manufacturing facilities and could be difficult to scale up rapidly in response to an emerging need such as a pandemic. It is usually necessary to adapt candidate vaccine viruses for high-yield growth in eggs, a process that can be time consuming, is not always successful, and can select receptor variants that may have suboptimal immunogenicity. In addition, agricultural diseases that affect chicken flocks, and that might be an important issue in a pandemic due to an avian influenza virus strain, could easily disrupt the supply of eggs for vaccine manufacturing. Therefore, development of alternative substrates for influenza vaccine production has been identified as a high-priority objective. One potential alternative method for production of influenza vaccine is expression of the influenza virus hemagglutinin (HA) using recombinant DNA techniques. This alternative avoids dependence on eggs and is very efficient because of the high levels of protein expression under the control of the baculovirus polyhedrin promoter.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | 0.5mL Intramuscular Injection | 0.5mL intramuscular injection on day 0 and day 21 in the deltoid muscle |
Timeline
- Start date
- 2010-06-01
- Primary completion
- 2011-10-01
- Completion
- 2011-10-01
- First posted
- 2010-06-22
- Last updated
- 2012-11-26
- Results posted
- 2012-11-26
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01147068. Inclusion in this directory is not an endorsement.