CompletedPhase 2NCT04008355
A Study to Assess Tolerability, Safety, Pharmacokinetics and Effect of AZP2006 in Patients With PSP
Studying Classic progressive supranuclear palsy syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- AlzProtect SAS
- Principal Investigator
- Philippe Verwaerde, PhDAlzProtect SAS
- Intervention
- AZP2006 oral solution(drug)
- Enrollment
- 36 enrolled
- Eligibility
- 40-80 years · All sexes
- Timeline
- 2020 – 2024
Study locations (3)
- Hôpital Salengro, Lille, Hauts-de-France, France
- Hôpital de la Fondation Adolphe de Rothschild, Paris, France
- Hôpitaux Universitaires Pitié Salpêtrière - Charles Foix, Paris, Île-de-France Region, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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