About this trial
The goal of this Phase 2 clinical trial is to investigate the efficacy and safety of NEU-411 in men and women aged 40-80 years with early Parkinson's Disease (PD) who have predicted elevations in the activity of the "leucine-rich repeat kinase 2" ("LRRK2" for short) pathway based on their genetic profile. A DNA test will be used to identify the "LRRK2-driven" population with predicted elevation in the LRRK2 pathway.
Eligibility criteria
Qualifiers
Aged 40-80 years at time of screening, inclusive
Diagnosis of clinically established or clinically probable Parkinson's Disease (PD)
LRRK2-driven PD using the investigational companion diagnostic genetic test (CDx)
Modified Hoehn and Yahr (mH&Y) of 1 to 2.5
Disqualifiers
Secondary or atypical parkinsonian syndromes
Uncontrolled diabetes mellitus with hemoglobin A1c (HbA1c) >8%
Other significant medical conditions (as determined by medical history, examination, or clinical investigations at screening)
Trial design
Treatments tested in this trial
- NEU-411
- Placebo