KARMET (ENT-01-030) - Efficacy of Orally Administered ENT-01 for the Treatment of Parkinson’s Disease-Related Constipation

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Multiple Dose Study to Evaluate Safety, Tolerability and Efficacy of Orally Administered ENT-01 for the Treatment of Parkinson’s Disease-Related Constipation

Recruitment Information:

Seeking volunteers with following diagnosis: PD, Control Volunteers Accepted Study Type: Interventional
Eligible Ages: 30 - 86 Status: No Longer Recruiting
Time Since Diagnosis: 6 years or more Study Focus: Constipation/Bladder Problems

Study Purpose:

To evaluate the safety, tolerability, and efficacy of repeated oral doses of ENT-01 for up to 25 days in subjects with Parkinson’s Disease-related constipation.

More Details

Patients will be randomized to active investigational treatment or placebo, and followed for approximately 70 days. Patients will have 6 visits to the clinic.

Phase: Phase 2 Lead Sponsor: Enterin, Inc
Trial ID: 006158 Sponsor Type: Industry
Primary Country: United States Additional Collaborators or Sponsors: N/A
Estimated Enrollment: 72 Study Start Date:
Estimated Study Completion Date: July 2019 Source:
Study Website:

More Inclusion & Exclusion Criteria

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