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Clinical Trial Summary

A phase 2 study to assess tolerability, safety, pharmacokinetics and effect of AZP2006 at different doses versus placebo on cerebrospinal fluid biomarkers in 36 patients with progressive supranuclear palsy. The patient study duration is 29 weeks including a washout period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04008355
Study type Interventional
Source AlzProtect SAS
Contact
Status Active, not recruiting
Phase Phase 2
Start date June 22, 2020
Completion date July 1, 2024

See also
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