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| ID | Type | Description | Link |
|---|---|---|---|
| 2009-014767-40 | EudraCT Number |
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| Name | Class |
|---|---|
| Quintiles, Inc. | INDUSTRY |
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A controlled, double-blind study to determine the immunogenicity and safety of influenza cell derived vaccine in elderly subjects.
This current phase II study is to pursue objectives similar to those of the ongoing adult phase II trial, but to expand into the elderly population who are more than 60 years of age. The results of this randomized, double blind, egg derived influenza vaccine (Influvac) - controlled, parallel-trial, in healthy elderly subjects are to be conducted over two consecutive years in multiple centers in Europe. At study initiation 600 subjects will be randomly allocated to receive the cell-derived or egg-derived influenza vaccine. At start of the second year subjects will be randomly re-allocated following stratification based upon the initial drug they were allocated and had received.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | 15 mcg hemagglutinin (HA) per viral strain; 0.5 mL single dose |
|
| 2 | Active Comparator | 15 mcg hemagglutinin (HA) per viral strain; 0.5 mL single dose |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Influenza Vaccine | Biological | surface antigen, inactivated, prepared in cell cultures |
| |
| Measure | Description | Time Frame |
|---|---|---|
| To assess the immunogenicity of the cell-derived subunit vaccine three weeks after vaccination, by applying the CHMP criteria for immunogenicity. | 3 weeks | |
| To assess the safety and tolerability of the cell-derived vaccine and compare to an egg-derived influenza vaccine. | 6 months | |
| To assess the safety and tolerability of the cell-derived vaccine following revaccination. | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| To assess the immunogenicity of the cell-derived subunit vaccine three weeks after revaccination, by applying the CHMP criteria for immunogenicity. | 3 weeks | |
| To assess the long-term immunogenicity (6 months) of the cell-derived subunit vaccine. | 6 months |
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Inclusion Criteria
Exclusion Criteria
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| Name | Affiliation | Role |
|---|---|---|
| Hanka de Voogd, MD | Abbott Healthcare Products B.V | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Site Reference ID/Investigator# 45005 | Benátky nad Jizerou | 294 71 | Czechia | |||
| Site Reference ID/Investigator# 45004 |
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| ID | Term |
|---|---|
| D007251 | Influenza, Human |
| ID | Term |
|---|---|
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D009976 | Orthomyxoviridae Infections |
| D012327 | RNA Virus Infections |
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| ID | Term |
|---|---|
| D007252 | Influenza Vaccines |
| ID | Term |
|---|---|
| D014765 | Viral Vaccines |
| D014612 | Vaccines |
| D001688 | Biological Products |
| D045424 | Complex Mixtures |
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| Influenza Vaccine |
| Biological |
surface antigen, inactivated, prepared in egg (influvac ®) |
|
| Hradec Králové |
| 500 03 |
| Czechia |
| Site Reference ID/Investigator# 45007 | Paide | 72713 | Estonia |
| Site Reference ID/Investigator# 45012 | Saku | 75501 | Estonia |
| Site Reference ID/Investigator# 45009 | Tallinn | 10617 | Estonia |
| Site Reference ID/Investigator# 45010 | Tallinn | 10617 | Estonia |
| Site Reference ID/Investigator# 45013 | Tartu | 51014 | Estonia |
| Site Reference ID/Investigator# 45017 | Kaunas | 47144 | Lithuania |
| Site Reference ID/Investigator# 45015 | Kaunas | 48259 | Lithuania |
| Site Reference ID/Investigator# 45016 | Kaunas | 49456 | Lithuania |
| Site Reference ID/Investigator# 45018 | Kaunas | 50009 | Lithuania |
| Site Reference ID/Investigator# 45019 | Klaipėda | 92231 | Lithuania |
| D014777 | Virus Diseases |
| D012140 | Respiratory Tract Diseases |