For more study specific information or to refer patients, please contact our research coordinators directly.
Antibodies Against Alpha-Synuclein (active; with limit anti-Parkinson's treatment)
This clinical trial is an approximately 20 week long study to evaluate whether a single dose of an investigational immunotherapy (antibody) drug given intravenously is safe and well-tolerated in PD patients. The drug is designed to bind to and remove the alpha-synuclein, which is believed to build up to abnormally high levels in the brains of subjects with PD. This is a single dose study involving a pre-dose lumbar puncture followed by 6 day / 5 night inpatient stay with 24 hour continuous heart monitoring and two post infusion lumbar punctures. Additional study activities include 3 MRIs, 1 DaTScan, clinical evaluations, neuropsychological testing, and blood sample collections. Eligible patients are between 40 - 80 years of age who have been diagnosed with Parkinson's disease for less than five years, have no motor fluctuations or dyskinesia's, are not receiving symptomatic PD treatment (no dopamine agonists/selegiline/rasagiline in last 3 months & no levadopa in last 30 days), and are willing to remain off symptomatic PD medications during study. For further information about this study, please contact our research coordinator email@example.com.
Neurodegenerative Disorders Cerebrospinal Fluid (CSF) Biorepository
The UCSD Movement Disorder Center is conducting a study to learn more about Parkinsonian diseases by collecting cerebrospinal fluid (CSF), the fluid that the brain sits in, samples for future research. Non-UCSD patients will first need to be seen at UCSD to confirm the diagnosis and medical history. Participation will include 1 study visit to complete a lumbar puncture. For more information please email: firstname.lastname@example.org
Interventional Studies: PD with Fluctuations
Dopamine Agonist for PD Patients with Fluctuations (Enrolling)
This Clinical trial is approximately 23 weeks/161 day long study comparing the effectiveness of a new D1/D5 Dopamine Agonist when taken with L-Dopa versus only taking L-Dopa alone for the management of "OFF" episodes. This new dopamine agonist may have the potential to reduce OFF time in subjects with PD who are experiencing significant OFF time despite their current dopaminergic therapy. Patients eligible for this study should have a meaningful response to L-Dopa with well- defined "OFF" time duration of >2.5 house during the waking day. Patients must be on at least 400mg/day of L- Dopa/day for 28 days prior to enrollment and should not have memory problems. For further information please contact our research coordinator email: email@example.com. See brochure
T-cell mediated autoimmune responses in PD (MJFF)
The research study's goal is to develop a biomarker of responsiveness to quantify alpha-synuclein (a-sin) responsive T cells in PD patients. Eligible participants would come in for one study visit to donate blood (250 mL).Please contact firstname.lastname@example.org for more information.
Patient Outcomes Project and Patient Registry Study
The goal of this program is to have a cohort of 500 patients followed at each center, with 200 patient data forms to be submitted within the next twelve months. This observational study only involves PD patients, whose medical history, UPDRS, H&Y, and other data will be collected. Currently enrolling established patients.
Contact Lisa Damron for more information at email@example.com.