Copernicus Podmiot Leczniczy Sp. z o.o.
Verified
Gdansk, Poland
Rare diseases
Investigational molecules
Locations
A plain-language summary of the goals, design and what participants do
This study involves people with Parkinson's Disease or Multiple System Atrophy, which are conditions that affect movement and other body functions due to problems with certain brain cells. The study uses a treatment called AB-1005, which is a gene therapy designed to deliver a protective protein to specific areas of the brain. During the treatment procedure, Carbidopa tablets are given by mouth and Fluorodopa (18F) is given through a vein as an injection. AB-1005 is given as a single injection directly into a part of the brain called the putamen.
The purpose of this study is to learn more about the long-term safety and how well AB-1005 works in people with these movement disorders. This is a follow-up study for people who are currently taking part in or have previously taken part in another study testing AB-1005. The study will track participants over many years to watch for any side effects and to see how their symptoms change over time.
During the study, participants will have regular check-ups where doctors will look for any unwanted effects of the treatment and measure how well participants can move and perform daily activities. For people with Parkinson's Disease, the study will track their motor symptoms, how much medication they need, and will use a special brain scan called 18F-DOPA PET to see how the brain is working. For people with Multiple System Atrophy, the study will measure movement abilities and quality of life using standard rating scales. The study will continue for several years to gather information about the long-term effects of this gene therapy treatment.
The trial runs in 6 steps – from screening to follow-up. Each step says what happens and what the team monitors.
5 criteria
3 criteria
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Gdansk, Poland
Katowice, Poland
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AB-1005 is a gene transfer therapy being studied for people with Parkinson's Disease or Multiple System Atrophy. This treatment works by delivering genetic material into the body to help manage the symptoms and progression of these movement disorders. The therapy is designed to provide long-term benefits by modifying how certain cells in the brain function.
Parkinson's Disease is a progressive disorder of the nervous system that affects movement control. The disease develops when certain nerve cells in the brain gradually break down or die, leading to a shortage of a chemical messenger called dopamine. Common symptoms include trembling of the hands, arms, legs, or face, stiffness of the limbs and trunk, slowness of movement, and problems with balance and coordination. As the disease progresses, symptoms become more pronounced and may interfere with daily activities. People with this condition may also experience changes in speech, writing difficulties, and reduced automatic movements such as blinking or swinging arms while walking. The progression of symptoms varies from person to person, and the disease typically worsens gradually over many years.
Multiple System Atrophy is a rare progressive disorder that affects multiple parts of the nervous system, including areas that control movement, blood pressure, and other automatic body functions. The disease occurs when certain brain cells deteriorate and die, particularly those involved in coordinating movement and regulating involuntary body processes. The Parkinsonian subtype of this condition primarily affects movement, causing symptoms similar to Parkinson's Disease such as slow movement, stiff muscles, tremors, and balance problems. As the disease advances, people may develop difficulties with coordination, speech, swallowing, and bladder control. Blood pressure may drop significantly when standing up, causing dizziness or fainting. The condition progresses more rapidly than Parkinson's Disease, with symptoms becoming increasingly severe over time.
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