drugset / Trial / NCT02642393

Summary

A multicenter, randomized, double-blind, placebo-controlled, phase 3 trial to determine whether oral inosine dosed to moderately elevate serum urate (from ≤5.7 mg/dL to 7.1-8.0 mg/dL) over 2 years slows clinical decline in early PD. Clinical decline will be assessed as change in the primary outcome variable of the Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS), a composite scale comprising patient- and clinician-reported outcomes.

Timeline

Start
2016-06
Primary completion
2019-06
Completion
2019-06

Outcome

Missed primary endpoint

registry analysis (other test); Inosine vs Placebo; p = 0.183; Slope 1.256 (95% CI -0.594 to 3.106); Mixed Models Analysis NCT02642393 ↗

paper did not result in a significant difference in the rate of clinical disease progression. PMID 34519802 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Inosine Unknown 500 mg Oral

Indications