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NCT Number: NCT06676644

Estimate the Safety and Effectiveness of Adjuvanted Influenza Vaccine Among Asian Elderly People When Compared to Non-adjuvanted Vaccines

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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Taiwan University Hospital

Taipei, 100225, Taiwan

Location status: Recruiting

Location contact

Jann-Tay Wang, PhD

CONTACT

[email protected]

+886-2312-3456 ext. 263517

Jann-Tay Wang, PhD

PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital Research Ethics Committee

CONTACT

[email protected]

+886-2312-3456 ext. 288576

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 65 years or above
  • Presence of at least 1 chronic medical condition associated with increased risk of complicated influenza, including hypertension, chronic obstructive pulmonary disease (group A, B, E), asthma, congestive heart failure (ACC/AHA stage A, B, C, D), coronary arterial disease, diabetes mellitus, chronic liver disease (Child-Pugh score A, B, C) or chronic kidney disease (stage 1~4), neuromuscular disorders, hematological or solid organ malignancies, recipient of hematopoietic stem cell transplantation or solid organ transplantation.

Exclusion criteria

  • Contraindications to influenza vaccination including history of severe adverse event after vaccination, such as anaphylaxis or Guillain-Barré Syndrome, or a severe bleeding tendency
  • Prior receipt of influenza vaccination during the current flu season.
  • Determination by the Principal Investigator (PI) that the participant is ineligible for enrollment based on clinical assessment.

Treatment and study plan

adjuvanted

Drug

adjuvanted (aIIV4) influenza vaccine in the Taiwanses elderly with chronic medical conditions

non-adjuvanted

Drug

non-adjuvanted (IIV4) influenza vaccine in the Taiwanses elderly with chronic medical conditions

Primary outcomes

  1. 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.

    Time frame: Measured through 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.

Secondary outcomes

  1. The geometric mean titer (GMT), seroprotection rate (SPR), cellular immune responses on Day1, Day 29 (±3), Day 181 (±7), and Day 361 (±7)

    Time frame: Measured through Day 361

    The geometric mean titer (GMT), seroprotection rate (SPR), cellular immune responses on Day1, Day 29 (±3), Day 181 (±7), and Day 361 (±7)

  2. Incidence of severe adverse reactions within 28 days after immunization.

    Time frame: Measured through Day 28

    Incidence of severe adverse reactions within 28 days after immunization.

  3. Incidence of laboratory-confirmed influenza during the study period.

    Time frame: Measured through Day 361

    Incidence of laboratory-confirmed influenza during the study period.

  4. Incidence of emergency department visits and hospitalizations related to respiratory illness, all-cause mortality during the study period.

    Time frame: Measured through Day 361

    Incidence of emergency department visits and hospitalizations related to respiratory illness, all-cause mortality during the study period.

Study contacts

Contact information is provided by the study sponsor or research team.

Jann-Tay Wang Clinical Professor, M. D., Ph.D.

CONTACT

[email protected]

+886-2-2312-3456 ext. 263517

Un-In Wu Clinical Associate Professor, M. D.

CONTACT

[email protected]

+886-2-2312-3456 ext. 265054

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

A Comparative Study on the Immunogenicity and Safety of Adjuvanted Versus Non-Adjuvanted Influenza Vaccines in the Elderly

Acronym: influenza

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Nov 6, 2024
Registry last updated
Feb 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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