RecruitingPhase 3NCT07498426

A Study to Evaluate the Efficacy of NIO752 in Participants With Progressive Supranuclear Palsy

Studying Classic progressive supranuclear palsy syndrome

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Key facts

Sponsor
Novartis Pharmaceuticals
Intervention
NIO752(other)
Enrollment
300 enrolled
Eligibility
41-81 years · All sexes
Timeline
20262031

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.

Open NCT07498426 on ClinicalTrials.gov

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