Supranuclear Ophthalmoplegia Clinical Trials

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The Progressive Supranuclear Palsy Clinical Trial Platform

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Biological, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The Progressive Supranuclear Palsy Clinical Trial Platform (PTP) is a multi-center, multi-regimen clinical trial evaluating the safety and efficacy of investigational products for the treatment of PSP.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 41
Maximum Age: 86
Healthy Volunteers: f
View:

• Clinical diagnosis of possible or probable PSP Richardson's Syndrome as defined by the 2017 Movement Disorder Society (MDS) criteria.

• Presence of PSP symptoms for ≤5 years at screening (based on the best judgment of the site PI).

• Mini-Mental State Examination (MMSE) score at screening of ≥25.

• Able to walk at least 10 steps with minimal assistance (e.g., one arm for safety, but not postural support).

• Stable doses of permitted medications as described per protocol for 30 days prior to screening.

• Resides at home or in the community (assisted living is acceptable).

• As assessed by the site PI, participant is likely to be able to comply with the protocol for the duration of the study, and has adequate vision, hearing (hearing aid permitted), and literacy (English or Spanish) sufficient for compliance with the required testing procedures.

Locations
United States
California
Stanford University
NOT_YET_RECRUITING
Palo Alto
University of California, San Diego
NOT_YET_RECRUITING
San Diego
University of California, San Francisco
RECRUITING
San Francisco
Massachusetts
Massachusetts General Hospital
NOT_YET_RECRUITING
Boston
New York
Albany Medical College
NOT_YET_RECRUITING
Albany
Rhode Island
Butler Hospital
NOT_YET_RECRUITING
Providence
Texas
Houston Methodist
NOT_YET_RECRUITING
Houston
Washington
University of Washington
NOT_YET_RECRUITING
Seattle
Contact Information
Primary
PSP Trial Platform Team
psptrialplatform@ucsf.edu
415-514-9420
Time Frame
Start Date: 2026-07-29
Estimated Completion Date: 2030-09-28
Participants
Target number of participants: 440
Treatments
Experimental: Regimen A: AADvac1
Participants are randomized to receive either active AADvac1 or matching placebo.
Experimental: Regimen B: LM11A-31
Participants are randomized to receive either active LM11A-31 or matching placebo.
Sponsors
Collaborators: University of Southern California, University of California, San Diego, Alzheimer's Clinical Trials Consortium, Massachusetts General Hospital, Alzheimer's Therapeutic Research Institute, National Institute on Aging (NIA)
Leads: Adam Boxer

This content was sourced from clinicaltrials.gov