Skip to main content
OpenTrials
Completed

NCT Number: NCT01737372

A Pilot Study to Assess microRNA Biomarkers in Early and Later Stage Multiple Sclerosis

This study will look at the blood and cerebrospinal fluid of consented participants who either have early stage multiple sclerosis (clinically isolated syndrome) or who have later stage (secondary progressive multiple sclerosis), or participants who do not have any neurological or autoimmune illness. Biomarkers and microRNA will be assessed for group differences.

Completed

Looking for future studies?

Notify Me

Key information

About this study

Multiple Sclerosis is a chronic autoimmune disorder of the central nervous system. While there are current immunomodulatory therapies that have been shown to be efficacious in the early stages of MS, these therapies are less potent in the later phases of MS. We can look at magnetic resonance imaging with gadolinium to measure active disease but it does not detect axonal degeneration. Therefore, there is a need to identify other biomarkers that may be used to diagnose MS and predict disease progression. Biomarkers found in the cerebrospinal fluid (CSF) are in closer proximity to the inflammatory lesion sites and are more sensitive.

This pilot study seeks to characterize differences in microRNA profiles and cell products in the early and later stages of MS, with the hope that that microRNA profiles could then be correlated to clinical and CSF inflammation indexes. CSF will be obtained from 45 participants.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • able to understand and agree to informed consent;
  • male or female patients 18-68 years of age
  • no disease modifying therapy 60 days prior to Baseline
  • EDSS score of less than or equal to 3.0 if a CIS patient; or less than or equal to 7.5 if SPMS patient
  • Labs within normal range no greater than 2 times the ULN or at the discretion of the PI
  • weight 46 kilograms to 127 kilograms inclusive
  • no active systemic infection
  • not currently pregnant or breast feeding
  • no history of corticosteroid treatment or relapse within 60 days prior to Baseline.

Exclusion criteria

  • not able to understand informed consent
  • if any of the inclusion criteria is not met
  • HIV infection, or current active Hepatitis B or C infection, positive HCVAb or HBsAG or HBcAB
  • positive pregnancy test
  • patient withdraws consent
  • Coumadin use within 60 days prior to Baseline

Treatment and study plan

Primary outcomes

  1. To characterize differences in microRNA profile and cell product patterns between early and later stage multiple sclerosis.

    Time frame: baseline

Secondary outcomes

  1. Correlate microRNA profiles with clinical and CSF inflammation indexes

    Time frame: baseline

Sponsors and collaborators

Lead sponsor

John F. Foley, MD

Other

Collaborators

  • Genzyme, a Sanofi Company

Registry information

Important dates

Study start
2012
Primary completion
2016
Study completion
2016
First posted
Nov 29, 2012
Registry last updated
Nov 9, 2016

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

View the official ClinicalTrials.gov record (opens in a new tab)

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.

Published trials that share one or more normalized conditions with this study.