RecruitingPhase 4NCT06928753

Real-world Effectiveness, Safety and Immunogenicity of Chikungunya Vaccination in Populations at Risk of Severe or Complicated Forms: Prospective Study in La Réunion


Sponsor

Centre Hospitalier Universitaire de la Réunion

Enrollment

1,800 participants

Start Date

Apr 18, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Against the backdrop of a growing chikungunya epidemic in La Réunion, this prospective study will assess the real-life efficacy, safety and immunogenicity of IXCHIQ® vaccine in vulnerable individuals (seniors, comorbid patients), defined by the French Health Autority (HAS) as at risk of severe or complicated forms and/or chronic disabling forms (chronic arthritis, chronic fatigue phenotypes). This study will also provide input for the preparation of a cluster randomized trial on a population scale.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Eligible for anti-chikungunya vaccination according to french Health Authority (HAS)
  • Beneficiary of social security coverage
  • Signature of informed consent form

Exclusion Criteria4

  • Pregnant women
  • Vaccine contraindication for patients undergoing medical treatment
  • Persons under guardianship, curatorship or safeguard of justice
  • Anyone who has received immunoglobulin or a blood or plasma transfusion 3 months prior to vaccine administration

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Interventions

BIOLOGICALIXCHIQ

Group of vaccinated arm will be with the IXCHIQ vaccine


Locations(1)

CHU La Réunion

Saint-Denis, France

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NCT06928753