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Natural History of Type 1 Interferonopathies: Insights From a European Cohort (EU-IFNp)

I

Imagine Institute

Status

Not yet enrolling

Conditions

Immune Dysfunction
Genetic Disease
Autoimmune Diseases
Neurological Diseases or Conditions

Study type

Observational

Funder types

Other

Identifiers

NCT07040774
HJ-24- EU-IFNp

Details and patient eligibility

About

Type I interferonopathies are rare autoinflammatory disorders caused by genetic defects and associated with significant morbidity and mortality. These diseases are refractory to conventional immunosuppressive therapies. They typically occur in childhood, although disease onset in adulthood has been observed. The clinical spectrum is wide and mainly involves the central nervous system. Joint involvement is also common, and more rarely, haematological features such as cytopenias or immunodeficiency may be observed.

Nearly all patients show consistent over-activation of the type I IFN pathway, as evidenced, the expression of IFN-stimulated genes, the so-called 'interferon signature'. To date, the natural history of interferonopathies remains unclear.

In this context, the establishment of a natural history of type I interferonopathy in patients is proposed to elucidate the pathophysiological mechanisms and identify biomarkers for diagnosis, prognosis, and disease activity, with the aim of better characterising the diversity of interferonopathies.

The main objective is to characterise the evolution of the pathology in paediatric and adult patients with type I interferonopathies.

The overall aim of this research is to propose therapeutic options tailored to patient phenotypes and to better define patient sub-groups in order to optimise the preparation of future clinical trials.

Enrollment

500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Genetically confirmed patient with type I interferonopathy
  • Patient affiliated to a social security scheme or beneficiary of such a scheme.

Exclusion criteria

  • Opposition of the patient and/or parental authority if the patient is a minor, to participation in the study.

Trial design

500 participants in 1 patient group

Patients
Description:
Patients with genetically confirmed type I interferonopathy

Trial contacts and locations

16

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Central trial contact

Marie-Louise FREMOND, Pr

Data sourced from clinicaltrials.gov

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