Clinical Trials Directory

Trials / Completed

CompletedNCT00067327

Treatment of Multiple Sclerosis Using Over the Counter Inosine

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
30 (planned)
Sponsor
National Center for Complementary and Integrative Health (NCCIH) · NIH
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether raising low levels of the natural antioxidant uric acid by the administration of a precursor, inosine, has any therapeutic effect on the progression of Relapsing Remitting Multiple Sclerosis (RRMS) and secondary progressive Multiple Sclerosis (MS).

Detailed description

Uric acid is a natural inhibitor of certain chemistries associated with peroxynitrite, a product of inflammation. In animal models of multiple sclerosis (MS), these chemical reactions have been associated with breakdown of the blood-brain barrier and CNS tissue damage. In addition, MS patients have serum uric acid levels that are lower than age- and sex- matched healthy individuals. The primary purpose of this study to determine whether raising low serum uric acid levels by daily oral administration of its precursor inosine has an effect on the cumulative number of newly active lesions on magnetic resonance imaging (MRI) and to evaluate the safety and tolerability of inosine in patients diagnosed with relapsing remitting and secondary progressive MS.

Conditions

Interventions

TypeNameDescription
DRUGInosine

Timeline

Start date
2002-02-01
Completion
2005-09-01
First posted
2003-08-19
Last updated
2006-03-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00067327. Inclusion in this directory is not an endorsement.