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Clinical Trials/NCT05526664
NCT05526664
Active, not recruiting
Not Applicable

Omics Gaucher Study: Multiomic Approach To Describe The Gaucher Disease Treatment Dynamics In Comparison To Untreated Healthy Volunteers

CENTOGENE GmbH Rostock1 site in 1 country25 target enrollmentOctober 6, 2022
ConditionsGaucher Disease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gaucher Disease
Sponsor
CENTOGENE GmbH Rostock
Enrollment
25
Locations
1
Primary Endpoint
OMICS DATA
Status
Active, not recruiting
Last Updated
10 months ago

Overview

Brief Summary

The study aims to investigate the transcriptomic and metabolomic changes in blood, plasma and isolated monocytes from Gaucher patients and healthy controls.

Detailed Description

Gaucher disease is one of the most common lysosomal storage disorders (LSD) and is an autosomal recessive inherited disorder, primed by mutation in the GBA1 gene which leads to a deficiency in β-glucocerebrosidase (GCase) activity and accumulation of its substrate glucosylceramide (GluCer)/-sphingosine (GluSph). The macrophages are the main cell type exhibiting a Gaucher disease phenotype. The large accumulation of GluCer and to a lesser extent that of GluSph lead to dysfunction in organs such as spleen, liver, bone marrow, and lungs. However, a validated, reproducible, and broadly applicable tool to classify Gaucher Disease at any stage of the disease is still missing. The development of new technologies, such as genomic analysis by next generation sequencing (NGS) and other "omics technologies," has advanced the molecular understanding and diagnosis of Rare Diseases The current study will analyze the transcriptional and metabolomic profiles in blood, plasma and isolated monocytes from Gaucher patients and healthy controls with the aim to compare these profiles and to define how much a patient profile differs from a healthy one.

Registry
clinicaltrials.gov
Start Date
October 6, 2022
End Date
December 1, 2025
Last Updated
10 months ago
Study Type
Observational
Sex
All

Investigators

Sponsor
CENTOGENE GmbH Rostock
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Gaucher Type 1 participants:
  • Informed consent
  • The participant is older than 18 years old
  • The participant was diagnosed with Gaucher Type 1 disease
  • Gaucher Type 3 participants:
  • Informed consent
  • The participant is older than 18 years old
  • The participant was diagnosed with Gaucher type 3 disease
  • Healthy participants:
  • Informed consent

Exclusion Criteria

  • Gaucher Type I participants:
  • The participant had any other clinically significant disease
  • The participant had a recent (within 14 days) acute infection and/or vaccination
  • Gaucher Type 3 participants:
  • Diagnosis of a significant CNS disease or cardiovascular disease other than Gaucher type 3
  • The participant had a recent (within 14 days) acute infection and/or vaccination
  • Healthy participants:
  • The participant had a recent (within 14 days) acute infection and/or vaccination

Outcomes

Primary Outcomes

OMICS DATA

Time Frame: 12 months

investigate the transcriptomic and metabolomic changes in blood, plasma and isolated monocytes from Gaucher patients and healthy controls.

Study Sites (1)

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