Efficacy, Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of BIA 28-6156 in GBA-PD
The purpose of this randomized, double-blind, placebo-controlled study is to assess the
efficacy of BIA 28-6156 over placebo in delaying clinical meaningful motor progression over
78 weeks in subjects with Parkinson's disease who have a pathogenic variant in the
g...
Age: 35 - 80 years
Gender: All
The Effect of a Lighting Intervention on Sleep in Parkinson Disease
50 participants with Parkinson's disease will be recruited to complete actigraphy studies to assess sleep disturbances. For this, participants will wear an Actigraph for seven days. Thirty of these participants with sleep disturbance will go on to receive a tailored lig...
Age: 18 years - 66+
Gender: All
Lighting Intervention to Improve Sleep
50 participants with Parkinson's disease will be recruited to complete actigraphy studies to assess sleep disturbances. For this, participants will wear an Actigraph for seven days. Thirty of these participants with sleep disturbance, will go on to receive a tailored li...
Age: 18 years - 66+
Gender: All
A Study to Assess if BIIB122 Tablets Are Safe and Can Slow Worsening of Early-Stage Parkinson's Disease in Participants With Specific LRRK2 Genetic Variants Between the Ages of 30 and 80 Using the Movement Disorder Society-Unified Parkinson's Disease Rating Scale
In this study, researchers will learn more about a study drug called BIIB122 in participants
with early-stage Parkinson's disease (PD). The study will focus on participants with a
specific genetic variant in their LRRK2 gene.
The main question researchers are tr...
Age: 30 - 80 years
Gender: All
Noninterventional Study Evaluating Parkinson's Disease Diary Use
This study aims to evaluate the impact of the frequency of assessments on the variability
over time, reliability, and compliance for the Parkinson's disease (PD) diary in patients
with PD in whom medications do not provide adequate control of symptoms.
Age: 39 - 70 years
Gender: All
A Study to Assess the Safety of BIIB122 Tablets and if it Can Slow the Worsening of Early-Stage Parkinson's Disease in Participants Between the Ages of 30 and 80
In this study, researchers will learn more about a study drug called BIIB122 in participants
with early-stage Parkinson's disease (PD). In this study:
- Participants will take 225 milligrams (mg) of BIIB122 or a placebo as tablets by mouth.
A placebo looks like ...
Age: 30 - 80 years
Gender: All
Open-label Safety Study of Dipraglurant (ADX48621) in Patients With Parkinson's Disease Receiving Levodopa-based Therapy
This open-label study is designed to assess the long-term safety and tolerability of
dipraglurant in PD patients for up to 52 weeks (at doses of 150-300 mg per day) for patients
that have completed an Addex sponsored double-blind clinical trial of dipraglurant.
Age: 30 - 85 years
Gender: All
Dipraglurant (ADX48621) for the Treatment of Patients With Parkinson's Disease Receiving Levodopa-based Therapy
This study is designed to evaluate the safety and efficacy of dipraglurant in PD patients
with dyskinesia (randomized 1:1 to receive active or placebo) for 12 weeks (1 week at 150 mg
per day and 11 weeks at 300 mg per day). The primary efficacy assessment will be ba...
Age: 30 - 85 years
Gender: All
STEM-Parkinson's Disease
This is a double-blinded, controlled, randomized clinical trial (RCT) to establish the safety
and efficacy of a non-invasive neuromodulation device for treating symptoms associated with
Parkinson's disease.
Age: 18 - 85 years
Gender: All
LRRK2, GBA and Other Genetic Biomarkers in Eastern European (Ashkenazi) Jews With and Without Parkinson's Disease
Single site observational study focused on elucidating the genes and biochemical pathways
involved in causing Parkinson disease.
Age: 30 years - 66+
Gender: All
PPMI Clinical - Establishing a Deeply Phenotyped PD Cohort
The Parkinson Progression Marker Initiative (PPMI) is a longitudinal, observational,
multi-center natural history study to assess progression of clinical features, digital
outcomes, and imaging, biologic and genetic markers of Parkinson's disease (PD) progression
...
Age: 30 years - 66+
Gender: All
Phase 1/2a Clinical Trial of PR001 (LY3884961) in Patients With Parkinson's Disease With at Least One GBA1 Mutation (PROPEL)
Study J3Z-MC-OJAA is a Phase 1/2a, multicenter, open-label, ascending dose, first in-human
study that will evaluate the safety of intracisternal LY3884961 administration in patients
with moderate to severe Parkinson's disease with at least 1 pathogenic GBA1 mutation...
Age: 35 - 80 years
Gender: All
A Clinical Trial Investigating the Efficacy, Safety and Tolerability of Continuous Subcutaneous ND0612 Infusion in Comparison to Oral IR-LD/CD in Subjects With Parkinson's Disease Experiencing Motor Fluctuations (BouNDless).
This is a multi-center, randomized, double blind, active controlled clinical Study. Following
a screening period, eligible subjects will be enrolled to an open-label oral IR LD/CD
adjustment period; then an open-label ND0612 conversion period; then after optimizatio...
Age: 30 - 80 years
Gender: All
Nilotinib in Parkinson's Disease
This study will assess the safety and tolerability of daily oral administration of nilotinib
(150-300mg once daily) in Parkinson's Disease.
Age: 40 - 79 years
Gender: All