Safety, Tolerability and Exploratory Efficacy of EC5026 in Parkinson's Disease (STEP Study)

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age50-80
SponsorEicOsis Human Health Inc.

About this trial

The goal of this clinical trial is to learn if the oral drug candidate EC5026 is safe and targets the correct pathways to treat Parkinson's Disease in adults. It will also learn about the levels of drug that are achieved in blood and in the fluid surrounding the brain (spinal fluid). The main questions it aims to answer are:

* Is EC5026 safe in adults with Parkinson's Disease? * What are the levels of EC5026 achieved after oral administration for 28 days? * What molecules or pathways does EC5026 target, and to what extent?

In addition, although it is not one of the primary aims of the study, this clinical trial will also explore if oral administration of EC5026 improves the symptoms of Parkinson's Disease.

Researchers will compare EC5026 to a placebo (a look-alike substance that contains no drug).

Participants will:

* Take EC5026 or a placebo every day for 28 consecutive days * Visit the clinic for frequent checkups, blood tests, spinal fluid tests, and questionnaires

Eligibility criteria

Qualifiers

Adult males and females, 50 to 80 years of age (inclusive) at the time of Screening.

Able to understand the consent form, and to provide voluntary written informed consent.

Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study-related procedures to complete the study.

Confirmed diagnosis of idiopathic Parkinson's Disease according to 2015 Movement Disorder Society (MDS) clinical diagnostic criteria.

Disqualifiers

Participants must have a negative urinary drug screen (UDS) for illicit drugs and a negative alcohol breath test.

Abstention from use of other investigative or non-approved drugs for the duration of the trial

Male participants who are not surgically sterile (vasectomized) and their female sexual partners must agree to use contraception during the study period and for 2 months after receiving the last dose of study drug.

Male participants must not donate sperm during the study and for 12 months after receiving the last dose of study drug.

Trial design

Treatments tested in this trial

  • EC5026 oral tablet
  • Placebo

Treatment groups

18 Participants
are divided into 3 treatment groups

Sponsors and collaborators

EicOsis Human Health Inc.

Lead sponsor

University of California, Davis

Collaborator

Michael J. Fox Foundation for Parkinson's Research

Collaborator