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A Study to Assess the Efficacy, Safety, and Pharmacokinetics of FNP-223 to Slow Progression of Progressive Supranuclear Palsy (PSP)

Testing FNP-223 for safety and effectiveness in slowing PSP progression.

Recruiting
50-80 years
All
Phase 2

Study Goal: This study, called the PROSPER trial, looks at how well a medication named FNP-223 works to slow down a disease called Progressive Supranuclear Palsy (PSP). Researchers will check if it's safe and how it affects the body over a year.

Who can join: People aged 50-80 with certain types of PSP can join. They need to have had PSP symptoms for 3 years or less. They also need to be able to walk at least 10 steps with little help and have a caregiver who can attend visits.

Who cannot join: People with other brain problems or specific PSP-related genetic issues cannot join. If they have had certain brain scans or tests that show other diseases, they also cannot join.

  • The study lasts for 52 weeks (1 year).
  • Participants will have regular check-ups to see how they are doing.
  • Caregivers need to be available to provide information about the participant's condition.

Participants will be assessed using tools like the PSP Rating Scale (PSPRS) to measure how the disease progresses. This study does involve some tests like brain scans and possibly lumbar punctures (a procedure to get fluid from the spine). All procedures will be discussed with participants before starting.

Study details
    Progressive Supranuclear Palsy

NCT06355531

Ferrer Internacional S.A.

11 May 2025

Step 1 Get in touch with the nearest study center
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  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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