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To compare the immunogenicity, cellular immune response, and safety between adjuvanted (aIIV4) and non-adjuvanted (IIV4) seasonal influenza vaccines in the Taiwanese elderly population with chronic medical conditions.
Annual influenza vaccination is the most important and cost-effective intervention in reducing the impact of influenza, and a key component of the WHO response and preparedness efforts for influenza of pandemic potential. Reduced effectiveness of conventional egg-based vaccination was observed among risk group, such as elderly and people on with chronic medical conditions, which may result from their impaired immunogenicity. WHO, as well as ACIP of the USA, Europe, and Australia suggested adjuvanted influenza vaccines as one of alternatives for those people, which could decrease the disease burden significantly in several analyses. An adjuvanted commercial vaccine has been approved in Taiwan recently, but the local data of safety and effectiveness analysis is limited. This 1-year randomized control trial is designed to estimate the safety and effectiveness of adjuvanted influenza vaccine among Asian elderly people when compared to non-adjuvanted vaccines.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| adjuvanted | Experimental | adjuvanted (aIIV4) influenza vaccine |
|
| non-adjuvanted | Active Comparator | non-adjuvanted (IIV4) influenza vaccine |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| adjuvanted | Drug | adjuvanted (aIIV4) influenza vaccine in the Taiwanses elderly with chronic medical conditions |
|
| Measure | Description | Time Frame |
|---|---|---|
| The seroconversion rate (SCR) measured by the change in hemagglutination inhibition (HI) titer against the vaccine strains in serum between Day 1 (pre-vaccination) and Day 29. | The seroconversion rate (SCR) measured by the change in hemagglutination inhibition (HI) titer against the vaccine strains in serum between Day 1 (pre-vaccination) and Day 29. | Measured through Day 29 |
| Measure | Description | Time Frame |
|---|---|---|
| The geometric mean titer (GMT), seroprotection rate (SPR), cellular immune responses on Day1, Day 29 (±3), Day 181 (±7), and Day 361 (±7) | The geometric mean titer (GMT), seroprotection rate (SPR), cellular immune responses on Day1, Day 29 (±3), Day 181 (±7), and Day 361 (±7) | Measured through Day 361 |
| Incidence of severe adverse reactions within 28 days after immunization. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jann-Tay Wang Clinical Professor, M. D., Ph.D. | Contact | +886-2-2312-3456 | 263517 | wangjt1124@ntuh.gov.tw |
| Un-In Wu Clinical Associate Professor, M. D. | Contact | +886-2-2312-3456 | 265054 | uninwu@gmail.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Taiwan University Hospital | Recruiting | Taipei | 100225 | Taiwan |
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| non-adjuvanted | Drug | non-adjuvanted (IIV4) influenza vaccine in the Taiwanses elderly with chronic medical conditions |
|
Incidence of severe adverse reactions within 28 days after immunization. |
| Measured through Day 28 |
| Incidence of laboratory-confirmed influenza during the study period. | Incidence of laboratory-confirmed influenza during the study period. | Measured through Day 361 |
| Incidence of emergency department visits and hospitalizations related to respiratory illness, all-cause mortality during the study period. | Incidence of emergency department visits and hospitalizations related to respiratory illness, all-cause mortality during the study period. | Measured through Day 361 |
| ID | Term |
|---|---|
| D007251 | Influenza, Human |
| ID | Term |
|---|---|
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D009976 | Orthomyxoviridae Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D012140 | Respiratory Tract Diseases |
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| ID | Term |
|---|---|
| C000718742 | GBP510 vaccine |
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