Study future

RSV (Respiratory Syncytial Virus)

ANIMA Research is conducting research into a study vaccine for Respiratory Syncytial Virus (RSV). RSV is a contagious virus that can affect anyone and can lead to serious respiratory diseases, especially in older adults.

What is RSV?
RSV (Respiratory Syncytial Virus) causes respiratory infections. In mild cases, the symptoms resemble those of a common cold, but RSV can be more serious in older people.

Common symptoms in older adults include:

  • Coughing, runny nose and sore throat
  • Shortness of breath or wheezing
  • Fatigue and general feeling of sickness
  • Fever and chills

Please note: RSV is different from influenza. Even if you have been vaccinated against influenza, you can still get an RSV infection.

Purpose of the study
The purpose of this study is to test an RSV study vaccine in adults aged 60 years and older. The study will investigate:

  • whether the vaccine is effective in preventing RSV infections
  • how safe and well tolerated the vaccine is
  • what the impact is on health and daily functioning

Participants receive optimal medical supervision and support from the ANIMA research center.

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Target

  • Men and women
  • Age: 60+ years

During a screening interview, we will assess whether you are eligible.

Program

  1. Screening visit
  2. Treatment period
  3. Follow-up visits

This study has been postponed until 2027 at the earliest!

Location

ANIMA Research
Alkerstraat 28-30-30A-32Z
3570 Alken, Belgium

or

ANIMA Research
Science Park 11-13
3590 Diepenbeek, Belgium

Reimbursement

There are no additional costs associated with participation.
All participants in a clinical study will receive compensation. The exact amount of compensation will be explained during the intake interview.

All personal data will be processed confidentially in accordance with applicable privacy legislation (GDPR). Your data will only be used for this study and will not be shared without legal or ethical grounds.

Approved by the UZA/UAntwerp Ethics Committee (reference 2026-8484, project ID 8370)