Multiple Sclerosis (MS) Clinical Trials

Find Multiple Sclerosis (MS) Clinical Trials Near You

From Genetics to Transcriptomics to Unravel the Mechanisms Behind a Poor Outcome in Multiple Sclerosis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

MS is a heterogeneous disease either in its response to treatment or clinical manifestation. Indeed, the natural history of MS is varying from a benign condition to a devastating and rapidly incapacitating disease. Clinical heterogeneity could also be cellular and / or molecular. The aim is to identify from OMIC analyses, at the early stage of the disease, differentially expressed molecules and / or cell subpopulations derived from CD8 + T lymphocytes and / or CD4 + T lymphocytes and / or B lymphocytes and monocytes from patients with aggressive versus non-aggressive, compared to a cohort of healthy controls

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ Common criteria for retrospective MS patients:

• Patients aged 18 years or older

• Clinical isolated syndrome (CIS) with or without dissemination in space

• Patients affiliated to an appropriate health insurance

⁃ Criteria for Aggressive MS group

⁃ • Start of a 2nd line therapy within the two years following the CIS

⁃ Criteria for Non aggressive MS group

• No conversion according to McDonald criteria from clinical isolated syndrome to multiple sclerosis within 2 years or

• Conversion based to McDonald criteria treated or not with first line disease modifying therapy within 2 years.

• Have a minimum of least 2 years of follow-up.

⁃ Healthy volunteers

• Aged 18 years or older

• No history of clinically isolated syndrome or MS

⁃ Pairing criteria :

• Age +/- 5 years

• Sex

⁃ Prospective MS Patients

• Patients aged 18 years or older

• Clinical isolated syndrome (CIS) with or without dissemination in space

• Patients affiliated to an appropriate health insurance

Locations
Other Locations
France
Nantes University Hospital
RECRUITING
Nantes
Contact Information
Primary
David LAPLAUD, PhD
david.laplaud@chu-nantes.fr
33 2 40 16 52 00
Time Frame
Start Date: 2022-01-24
Estimated Completion Date: 2029-07-24
Participants
Target number of participants: 130
Treatments
Other: Retrospective Aggressive MS patients
Patients from who the clinical outcome is already known and classified as poor based on study definition detailed in inclusion criteria (retrospective arm). Blood sample collected after first event is available and used to characterize OMIC profile of T and B cells involve in MS.
Other: Retrospective Non Aggressive MS patient
Patient from who the clinical outcome is already known and classified as non-aggressive based on study definition detailed in inclusion criteria (retrospective arm). Blood sample collected after first event is available and used to characterize OMIC profile of T and B cells involve in MS.
Other: Healthy volunteers
Prospective arm use as comparator.
Other: Prospective MS patients
MS patients from who the clinical outcome will be established at the end of the follow up. Blood sample will be collected after the first event to validate molecules of interest from OMIC results by using FACS a different technology and classify MS patient.
Related Therapeutic Areas
Sponsors
Leads: Nantes University Hospital

This content was sourced from clinicaltrials.gov