Authorised Therapeutic use (Phase IV) Incident dementia

A phase IV trial of Shingrix on incident dementia diagnosis in adults aged ≥76 years in Finland

EU CTIS ID: 2025-524598-17-00

What this study is testing

1. To assess the effect of Shingrix on the risk reduction of an incident dementia diagnosis among adults ≥ 76 years, compared to placebo.

  • Therapeutic use (Phase IV)

A plain-language read of the study's public EU CTIS listing. The study team confirms the details.

Who can take part

You may be able to join if

  • Participants are eligible to be included in the study only if ALL of the following criteria apply: 1. Citizens living permanently in Finland, who, in the opinion of the investigator, can and will comply with the requirements of the protocol (e.g., return for follow-up visits).
  • 2. Written or witnessed informed consent obtained from the participant prior to performance of any study-specific procedure.
  • 3. Age 76 years or older at the time of signing the informed consent.

You likely can't join if

  • Participants will be excluded from the study if any of the following criteria apply: 1. History of vaccination against HZ
  • 2. History of dementia prior to enrolment, including confirmed cases or those under investigation. This includes: a) History of a confirmed clinical diagnosis of dementia prior to enrolment b) Prior or current use of medications intended to treat dementia c) Current or recent history of cognitive assessments for any memory deficit or suspected dementia before enrollment including investigations that are ongoing or were inconclusive (but not those for which dementia was conclusively ruled out); MCI on its own without any other information to indicate cognitive decline or dementia will not result in exclusion
  • 3. Severely immunocompromised individuals (i.e., those with haematological cancer or have had stem cell transplant or organ transplant)
  • 4. Concurrently participating in another clinical trial, in which the participant has been or will be exposed to an investigational product
  • 5. Known systemic hypersensitivity to any of the vaccine components, or history of a life-threatening reaction to the vaccines used in the study or to a vaccine containing any of the same substances
  • 6. Living in a nursing facility

The study team makes the final eligibility decision.

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 65+ years. The study team makes the final eligibility decision.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.