This is a study to understand if taking VTX3232 is safe in participants diagnosed with early stage idiopathic Parkinson's Disease (PD). Approximately 10 patients will take VTX3232 Dose A. The study consists of a 30-day Screening Period (to see if a participant qualifies for the study), a 7-day Pre-Baseline Period, a 28-day Open Label Treatment period (a participant receives active Dose A), and a 14-day Follow-Up Period.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
11
Dose A
Local Site #840001
New Haven, Connecticut, United States
Adverse Event (AE) / Serious Adverse Event (SAE) Incidence Rate and Severity through study completion
Incidence of AEs and SAEs
Time frame: Day 1 of treatment period through study completion, up to 6 weeks
Pharmacokinetics (PK) of VTX3232 in plasma and Cerebrospinal Fluid (CSF) at Day 28
Concentration of VTX3232 in plasma and CSF through 28 days of study treatment
Time frame: Day 1 of treatment period to Day 28 of treatment period
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.