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Trial intelligence / Profile preview
NCT00067327Phase 2
Key facts
Phase 2, randomised trial of inosine in multiple sclerosis (MS), sponsored by National Center for Complementary and Integrative Health. Primary endpoints: Cumulative number of newly active lesions on MRI and Safety and tolerability of inosine. Started Feb 2002; status: completed.
Inosine
Patients receiving daily oral administration of inosine to raise serum uric acid levels.
Patients with clinically definite RRMS or probable MS with recent relapse and MRI lesions, EDSS <= 5.0, and low serum uric acid (< 5 mg/dl), excluding those on recent immune-modifying treatments or corticosteroids.
Cumulative number of newly active lesions on MRI
Safety and tolerability of inosine
Beyond the preview
Full results, competitive context and analysis are in the Gosset platform.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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