LM11A-31 for Progressive Supranuclear Palsy
What You Need to Know Before You Apply
What is the purpose of this trial?
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. Regimen B will evaluate the safety and efficacy of a single study drug, LM11A-31, in participants with PSP.
Who Is on the Research Team?
Anne-Marie Wills, MD
Principal Investigator
Massachusetts General Hospital
Adam Boxer, MD, PhD
Principal Investigator
University of California, San Francisco
Irene Litvan, MD
Principal Investigator
University of California, San Diego
Julio Rojas-Martinez, MD, PhD
Principal Investigator
University of California, San Francisco
Are You a Good Fit for This Trial?
This trial is for people diagnosed with possible or probable Progressive Supranuclear Palsy (PSP) Richardson's Syndrome, who have had symptoms for 5 years or less. Participants must be able to walk at least 10 steps with minimal help, live at home or in the community, and have good enough vision, hearing, and thinking skills to take part.Inclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- LM11A-31
Trial Overview
The study is testing a new drug called LM11A-31 compared to a placebo (inactive pill) in people with PSP. The goal is to see if LM11A-31 is safe and effective. Participants are randomly assigned to receive either the drug or placebo.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Find a Clinic Near You
Who Is Running the Clinical Trial?
Adam Boxer
Lead Sponsor
Alzheimer's Therapeutic Research Institute
Collaborator
PharmatrophiX Inc.
Industry Sponsor
Massachusetts General Hospital
Collaborator
University of Southern California
Collaborator
University of California, San Diego
Collaborator
Alzheimer's Clinical Trials Consortium
Collaborator
National Institute on Aging (NIA)
Collaborator
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