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Completed NCT00385710

Trial of Valproic Acid in Patients With Progressive Supranuclear Palsy (Depakine)

Conditions: Progressive Supranuclear Palsy

Sex: All
Ages: 45 Years – 75 Years
Healthy volunteers: No
Phase: PHASE2
Enrollment: 28
Sponsor: Nantes University Hospital

Location: Service de Neurologie A, Hôpital Gabriel Montpied-BP Clermont-Ferrand

Summary

Progressive Supranuclear Palsy (PSP) is a relentlessly progressive neurodegenerative disorder, clinically characterized by parkinsonism with prominent axial involvement and postural instability, bulbar symptoms, supranuclear ophthalmoplegia, and executive dysfunction. Abnormal neuronal and glial tau aggregations affecting the basal ganglia and selective brainstem structures result in dysfunction of the five frontosubcortical circuits and brainstem functions. There is no effective treatment for PSP. One of the key feature in the aggregation of tau is its phosphorylation by kinases such as glycogen synthase kinase 3b (GSK3b). Recent reports have shown that valproic acid was able to inhibit the activity of GSK3b and could exert a neuroprotective effect through this inhibition. The investigators thus decided to conduct this controlled study to assess the putative neuroprotective effects in patients with PSP.

Eligibility Criteria

Inclusion Criteria: * Patients with possible or probable PSP * from 45 to 75 year of age

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT00385710). StuddyBuddy aggregates publicly available trial information.