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A Phase II, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of CVN424 in Parkinson’s Disease Patients With Motor Fluctuations


Brief Summary:

This is a phase 2 study, randomized, double-blind, placebo-controlled, multicenter study of
oral CVN424 at two dose levels (low-dose and high-dose) in Parkinson’s disease (PD) patients
with motor fluctuations.


Inclusion Criteria:

– Male or female adult who is 30 to 80 years of age inclusive at study entry.

– Has idiopathic Parkinson’s disease, Hoehn and Yahr stages 2-4, and is on a stable
dosage of levodopa.

– Experiences an average of at least 2 h total OFF time/day, and at least 1 h each day,
per Patient Motor Diary over 2 days during Screening assessment.

– The subject signs and dates a written informed consent form (ICF) and any required
privacy authorization prior to the initiation of any study procedures.

Exclusion Criteria:

– Has atypical parkinsonism, severe disabling dyskinesia, or severe motor fluctuations
that the investigator considers likely to interfere with study participation or
assessments, or history of implant for Deep Brain Stimulation.

– Poor concordance (<75%) of self-report with site rater on in-clinic Screening period Patient Motor Diary. Subjects with low concordance may be retested after further instruction, at investigator's discretion. - Screening period Patient Motor Diary scored at-home over 2 days demonstrates unacceptable quality of the diary, with more than 4 errors per day. (Assistance from caregivers is permitted if they also will be providing assistance with home Patient Motor Diary entries for Day 15 and 27 efficacy assessments.) Subjects with more than 4 errors per day may be retested after further instruction, at investigator's discretion. - Body mass index (BMI) at Screening <18.0 or >35.0 kg/m2, inclusive.

– Subject has evidence of Clinically significant neurologic or other disorder or
impairment that, in opinion of Investigator, is reasonably expected to impact the
ability of the subject to participate or to confound the study results.

– Subject has current or recent (within 6 months) gastrointestinal disease that would be
expected to influence the absorption of drugs (i.e., a history of malabsorption, any
surgical intervention known to impact absorption [e.g., bariatric surgery or bowel

– Subject has a history of cancer or other malignancy, with the exception of low-grade
cervical intraepithelial neoplasia, low-grade (low-risk) prostate cancer, or 5-year
cancer-free survivors of basal or squamous cell carcinoma, higher-grade cervical
intraepithelial neoplasia or prostate cancer.

– Has a history of human immunodeficiency virus (HIV) infection.

– Subject has a supine blood pressure outside the ranges of 80 to 160 mm Hg for systolic
and 50 to 100 mm Hg for diastolic, confirmed with up to two repeat tests, at the
Screening Visit; or symptomatic orthostatic hypotension, in the opinion of the

– Subject has a resting heart rate outside the range 50 to 100 bpm, confirmed with up to
two repeat tests, at the Screening Visit.

– Positive urine result for illegal drugs (except cannabis) at Screening, or history of
illegal drug use (except cannabis) or alcohol abuse within 1 year prior to the
Screening Visit.

– Subject has received any investigational compound (defined as a drug that has not been
FDA-approved) within 30 days prior to the first dose of study medication, or within 5
half-lives of the investigational compound, whichever is greater.

– Subject has, within the prior month, ingested any excluded medication, supplements, or
food products listed in the Excluded Medications and Dietary Products table as listed
in Table 2.

– Male subjects who do not agree to all the following rules: when sexually active with
female partner(s) of childbearing potential during the study and for 12 weeks after
the last dose of study drug: a) use an acceptable method of birth control (condom with
spermicide or surgical sterilization) and b) refrain from sexual activity with female
partners who do not use an acceptable method of birth control. Barrier contraception
(condom with spermicide) must be used by all male subjects who were not surgically
sterilized at least 90 days prior to screening. Male subjects must also agree to
refrain from sperm donation during the study and until 12 weeks after the last dose of
study drug.

– Female subjects who are pregnant or breastfeeding or plan to become pregnant or donate
ova during the study or for 30 days after the last dose of study drug. Women of
childbearing potential (WOCBP) also must be practicing an adequate method of birth
control (e.g., oral or parenteral contraceptives, intrauterine device, barrier,

– Risk of suicide according to the investigator’s clinical judgment or has made a
suicide attempt in the previous 3 years.

– Subject is a study site employee or an immediate family member of a study site


  • Collaborative Neuroscience Network, LLC, Long Beach, California, United States, 90806
  • SC3 Research – Pasadena, Pasadena, California, United States, 91105
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