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RT001 in Patients With Progressive Supranuclear Palsy (PSP) PROGRESSIVE SUPRANUCLEAR PALSY

Progressive Supranuclear Palsy Clinical Trial

Official title:
A Randomized, Double-blind, Controlled, Phase 2 Study to Assess Efficacy, Long Term Safety and Tolerability of RT001 in Subjects With Progressive Supranuclear Palsy

Clinical Trial Summary

This is a randomized, placebo-controlled trial of RT001 in patients with PSP.

Clinical Trial Description

This is a randomized, placebo-controlled trial of RT001 in patients with PSP to assess the efficacy, safety and tolerability of RT001. Subjects will be randomized to RT001 or placebo and will receive study drug for 48 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04937530
Study type Interventional
Source Retrotope, Inc.
Contact Mark G. Midei, MD
Phone (650) 437-0700
Email mark@retrotope.com
Status Recruiting
Phase Phase 2
Start date June 23, 2021
Completion date August 30, 2022
View Details
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