Minzasolmin for Parkinson's Disease
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called minzasolmin (also known as UCB0599) to observe its effects on the brain in individuals with newly diagnosed Parkinson's disease. Researchers aim to understand the differences between starting the medication immediately versus delaying it. Participants will receive either a high or low dose of minzasolmin. This trial is for individuals who have already completed a prior study with the same medication. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.
Do I have to stop taking my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study team or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that minzasolmin (UCB0599) is generally safe and well-tolerated. In one study, 94 participants, including both healthy individuals and those with Parkinson's disease, received different doses of minzasolmin. The results indicated that most participants handled the treatment well. No major safety issues arose, and the side effects were expected and manageable. These findings are promising for those considering joining a clinical trial for minzasolmin. However, consulting a healthcare professional is always important if there are questions about participating in a clinical trial.12345
Why are researchers excited about this trial's treatments?
Researchers are excited about minzasolmin (UCB0599) because it targets a new pathway in Parkinson's disease treatment. Most current treatments, like levodopa, focus on replacing dopamine or managing symptoms. However, minzasolmin aims to slow disease progression by inhibiting alpha-synuclein aggregation, a protein linked to the condition's underlying cause. This approach could potentially modify the disease itself, not just alleviate symptoms. The trial is testing both high and low doses to find the most effective treatment option.
What evidence suggests that minzasolmin could be an effective treatment for Parkinson's disease?
Research has shown that minzasolmin (UCB0599) is under study as a potential treatment for Parkinson's disease. It targets a protein called alpha-synuclein, linked to the disease. The treatment aims to slow Parkinson’s progression by preventing this protein from misfolding. Earlier studies suggested that minzasolmin might help reduce issues with alpha-synuclein, potentially protecting brain function. However, the major study ORCHESTRA did not meet its primary goals and showed no clear effect on Parkinson's symptoms. Despite these mixed results, research continues to explore minzasolmin's potential benefits. Participants in this trial will receive either a high or low dose of minzasolmin (UCB0599) to further investigate its effects.23678
Who Is on the Research Team?
UCB Cares
Principal Investigator
001 844 599 2273
Are You a Good Fit for This Trial?
This trial is for people with early-stage Parkinson's disease who completed a prior study (PD0053) and can start this one within 4 weeks of the last. Participants must agree to contraception use and not plan pregnancy or sperm donation during and after the trial. They should be able to consent and follow study rules.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive either a high or low dose of minzasolmin (UCB0599) to evaluate its long-term efficacy, safety, and tolerability
Follow-up
Participants are monitored for safety and effectiveness after treatment
Open-label extension
Participants may continue to receive the study drug to further assess long-term effects
What Are the Treatments Tested in This Trial?
Interventions
- UCB0599
Find a Clinic Near You
Who Is Running the Clinical Trial?
UCB Biopharma SRL
Lead Sponsor
Jean-Christophe Tellier
UCB Biopharma SRL
Chief Executive Officer since 2015
MD from University of Reims Champagne-Ardenne, Rheumatology specialization from University of Paris V, Executive business programs at Harvard and INSEAD
Dr. Iris Loew-Friedrich
UCB Biopharma SRL
Chief Medical Officer since 2014
MD from University of Leuven, PhD in Medical Sciences from University of Leuven