Early Parkinson's Disease Monotherapy With CVN424

Exclusion Criteria

• •Diagnosis of secondary or atypical parkinsonism.
• •Diagnosis of parkinsonian motor signs or symptoms ≥ 4 years before Screening Visit.
• •Previous surgical procedure for PD.
• •Prior treatment with a dopamine agonist, levodopa, monoamine oxidase B (MAOB) inhibitor, or adenosine A2A receptor antagonists for more than 28 total days prior to screening. Additional exclusionary parameters around PD treatment include:
• •Treatment with a dopamine agonist within 14 days of Screening.
• •Treatment with a MAOB inhibitor within 90 days of Screening.
• •Current use of any antipsychotic, metoclopramide, or reserpine. If previously used, this may not have been within 28 days of Screening or 5 elimination half-lives (whichever one is longer).
• •Current use of potent Cytochrome P450 (CYP) 3A4/5 inhibitors or inducers.
• •Clinically significant orthostatic hypotension.
• •Clinically significant hallucinations requiring antipsychotic use.
• •Known autoimmune, malignancy (except basal cell carcinoma) or hematologic disease (prior or current) likely to interfere with the safe participation of the participant or interfere with assessment of safety or efficacy based on the opinion of the investigator and the medical monitor.
• •Any clinically significant medical, surgical, or psychiatric abnormality that, in the judgment of the Investigator, is likely to interfere with study compliance, the safe participation of the participant or the assessment of safety or efficacy.
• •Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels greater than 2 times the upper limit of normal (ULN), and total bilirubin greater than 1.5 times ULN.
• •Participants with Gilbert's syndrome may have direct bilirubin measured and would be eligible for this study provided that direct bilirubin is ≤ 1.5 times ULN.
• •Significant renal impairment as determined by estimated glomerular filtration rate (eGFR) using creatinine clearance (CrCL) as per the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation of ≤ 50 milliliters per minutes (mL/min).
• •Participant has an ECG, prior documentation history, or clinical evidence of potentially unstable heart disease, including, but not limited to the following:
• •1. QT interval corrected using Fridericia's formula (QTcF) \> 470 milliseconds (msec) for female participants; \> 450 msec for male participants
• •2. Complete right or left bundle branch block
• •3. Myocardial infarction within 1 year prior to screening, unstable angina within 6 months, or a current concern for symptomatic ischemic heart disease in the opinion of the investigator
• •4. Clinically significant atrial or ventricular dysrhythmia; the heart must be in predominantly normal sinus rhythm
• •5. Second- or third-degree atrioventricular (AV) block
• •6. New York Heart Association (NYHA) Class II or higher congestive heart failure
• •7. Clinically significant cardiomyopathy or cardiac structural abnormality, in the opinion of the investigator
• •8. Any other cardiac condition that the Investigator feels may predispose the participant to ischemia or arrhythmia
• •Current (or within past 12 months) diagnosis or history of substance abuse (excluding nicotine or caffeine) by Diagnostic and Statistical Manual of Mental Disorders 5 criteria.
• •Positive urine drug screen for tetrahydrocannabinol or any drugs that may affect participant safety or interfere with efficacy assessments.
• •Medical or recreational use of marijuana within 2 months of the Screening Visit. Use of cannabidiol (CBD) is prohibited after the Screening Visit and throughout the study.
• •Currently active major depression as determined by Beck Depression Inventory (BDI)-II score of \> 19.
• •Active suicidal ideation within 1 year prior to Screening Visit as determined by a positive response to Question 4 or 5 on the C-SSRS.
• •Currently lactating or pregnant, or planning to become pregnant during the study.
• •Current participation in another investigational clinical study and/or receipt of any investigational drug within 90 days prior to Screening.
• •Prior use of CVN424 investigational product.
• •Positive test for coronavirus disease 2019 (COVID-19). A participant who tests positive for COVID-19 will be eligible to be rescreened once result is negative.
• •Positive test for human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) consistent with current infection.