drugset / Trial / NCT07170475

A Phase Ib Trial of Combined Febuxostat and Inosine Therapy in Patients With Parkinson's Disease

NCT07170475

Phase 1 Recruiting 24 enrolled Fujita Health University
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will test the safety of twice-daily oral dosing of combined febuxostat and inosine in 24 patients with Parkinson's disease. Participants will receive one of the four regimens, taken twice daily for 12 weeks: Who can join: Adults with early-stage Parkinson's disease on stable medication regimens. What participants do: * Take their assigned dose twice daily (morning and evening) for 12 weeks. * Visit the clinic at baseline and weeks 4, 8, and 12 for blood tests (including hypoxanthine), exams, and questionnaires. * Keep a simple diary of any side effects or changes in daily activities. Risks and benefits: Possible side effects include mild gastrointestinal upset, headache, or elevated uric acid levels. While direct benefit is not guaranteed, this safety data will inform future Parkinson's disease treatments. Learn more: Contact \[site-specific contact info\] for details on eligibility and enrollment.

Timeline

Start
2025-06-27
Primary completion
2026-03-31
Completion
2026-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Febuxostat Small molecule Oral
Subject Inosine Unknown Oral

Indications