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NCT Number: NCT04024774

Diagnostic Research in Patients With Rare Diseases -Solving the Unsolved Rare Diseases

Most diagnostically unsolved rare disease have a genetic cause. These causes have not been found applying the current methodologies due to technical limitations (e.g. repeat expansions, changes in non-coding (intronic) regions) or, although methodically recorded, their pathophysiological significance but not classified as clinically relevant. A re- and meta-analysis of existing data sets with new algorithms and statistical models as well as the complementation with other omics technologies followed by functional follow-up studies in appropriate disease models (e.g. patient cell lines) allows to elucidate additional causes of diseases and improve the diagnosis of hereditary diseases. In addition to the direct examination of persons affected, the analysis of healthy family members, for example of parents, plays an important role in a so-called trio analysis, especially in the efficient filtering of the extensive data sets for newly created changes, so-called de novo- Variants (new mutations). In the context of the outlined analyzes, new disease genes can be found and validated. The gain of scientific knowledge due to a better understanding of basic cell biological mechanisms can contribute to the development of targeted therapeutic approaches.

In this context, the Solve-RD project has been built and financed by the European Union with the ambitions to solve large numbers of rare disease, for which a molecular cause is not known yet by sophisticated combined omics approaches, and to improve diagnostics of rare disease patients. Solve-RD fully integrates with the newly formed European Reference Networks (ERNs) for rare diseases, and in particular the ERN-RND, -EURO-NMD, -ITHACA, and -GENTURIS. The AnDDI-Rares network is fully affiliated to the ERN ITHACA network and will actively contribute to the project, by the ambition of sharing knowledge about genes, genomic variants and phenotypes.

The project will first reanalyse 18.000 negative exomes from the different ERNs performed in a diagnostic or research context (collection of biomaterial, clinical/phenotypic data plus next-generation sequencing has already been performed, and the patient/family has agreed previously in writing that their sample could be used for research related to their disease, with no study related presence required. The project will also propose new multi-omics analyses with new samples needed in 500 patients and their parents in total, justifying the AnDDI-Solve-RD project.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU de Dijon

Dijon, 21079, France

Location status: Recruiting

Location contact

Laurence OLIVIER-FAIVRE

CONTACT

[email protected]

03.80.29.53.13

laurence OLIVIER-FAIVRE

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Persons or legal guardian who have given their written informed consent
  • Unclear molecular cause of the disease corresponding to the list of diseases selected by the Solve-RD data interpretation force (principal investigator part of the team)
  • Suspected genetic cause of the disease with negative exome reanalysis
  • Healthy parents available for trio analysis

Exclusion criteria

  • Person not affiliated to a national health insurance scheme

Treatment and study plan

biological samples

Biological

blood samples, urine samples, tissue samples

Genetic Test

Genetic

anamnesis and NGS sequencing

Primary outcomes

  1. Molecular genetic

    Time frame: Day 1

    Verification of the genetic causes of unclear genetic diseases

Secondary outcomes

  1. Number of diagnoses

    Time frame: Day 1

    Improve number of diagnoses of unclear syndromes

  2. Characterization of gene defects

    Time frame: Day 1

    Further characterization of the identified gene defects

  3. Number of patients receiving appropriate therapy after successful diagnosis

    Time frame: Day 1

Study contacts

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

Laurence OLIVIER-FAIVRE

CONTACT

[email protected]

03.80.29.53.13 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Dijon

Other

Registry information

Acronym: AnDDI-Solve-RD

Important dates

Study start
2019
Primary completion
2026
Study completion
2026
First posted
Jul 18, 2019
Registry last updated
Apr 2, 2025

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

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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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