A Phase 2 Study and Open-Label Extension of NEU-411 in Companion Diagnostic-Positive Participants With Early Parkinson's Disease

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age40-80
SponsorNeuron23 Inc.

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

Treatment groups

150 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Neuron23 Inc.

Lead sponsor

Qiagen Manchester Limited

Collaborator

Roche Diagnostic Ltd.

Collaborator