Orally Administered ENT-01 for Parkinson's Disease-Related Constipation Follow-on Safety "Roll-over" Study (Rollover)

Stopped early · Phase 2

Conditions studied: Parkinson Disease, Constipation

In brief

This study will be conducted as an open-label safety follow-on to a multi-center, double-blind, randomized study. All subjects who participated in the randomized study will be offered participation in this unblinded, single-arm, safety study. Approximately 50 subjects will be entered into the study and ENT-01 will be administered daily in escalating doses followed by a fixed dose for 12 weeks. Each subject will participate for approximately 20 weeks; dosing duration will be approximately 14 weeks.

Key facts

Study ID

NCT04483479

Run by

Enterin Inc.

People needed

27

Starts

2020-07-30

Expected to finish

2022-02-17

Last updated by the study team

2024-03-19

Who can join

Age: 30 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All subjects who participated in the randomized study ENT-01-030 (KARMET Stage 2 Extension subjects) and who completed the dosing period.
• Subjects aged 30-90 years at the time of screening for the ENT-01-030 study, both genders
• Subjects must provide informed consent and be willing and able to comply with study procedures.
• Subjects must be able to read, understand, and accurately record data into the diary to guarantee full participation in the study.
• Female subjects must have negative serum or urine pregnancy tests and must not be lactating. For females able to bear children, a hormonal (i.e., oral, implantable, or injectable) and single-barrier method, or a double-barrier method of birth control must be used throughout the study. A vasectomized partner will be allowed as one in conjunction with another single-barrier method.
• Female subjects unable to bear children must have this documented in the CRF (i.e., tubal ligation, hysterectomy, or postmenopausal [defined as a minimum of one year since the last menstrual period]). Post-menopausal status will be confirmed by follicle stimulating hormone (FSH) in women less than 60 years of age.

You may not qualify if…

• Unable or unwilling to provide informed consent or to comply with study procedures.
• Unable to withdraw proton pump inhibitors.
• Unable or unwilling to withdraw from laxatives, opiates, clonazepam, or any medications which may cause constipation 2 weeks prior to the dose adjustment period and throughout the rest of the study.
• Diagnosis of secondary constipation beyond that of Parkinson's disease.
• A compromised gastrointestinal system which includes:
• Structural, metabolic, or functional GI diseases or disorders.
• Acute GI illness within 2 weeks of the screening visit.
• History of major GI surgery within 30 days of the screening visit (a history of cholecystectomy, polypectomy, hernia repair or appendicectomy are not exclusionary as long as they were performed more than 30 days before the screening visit).
• Neurological disorder other than Parkinson's disease that in the opinion of the investigator might interfere with the conduct of the study.
• On treatment with intra-jejunal dopamine or carbidopa/levodopa (i.e. Duopa).
• Subjects starting a new Parkinson's disease medication or modifying an existing medication within 2 weeks prior to enrollment.
• Unable to maintain a stable diet regimen.
• Subjects with a cognitive impairment that preclude them from understanding the informed consent.
• Subjects placed under legal guardianship.
• History of excessive alcohol use or substance abuse.
• Any clinically significant abnormalities on screening laboratories or physical examination requiring further evaluation or treatment.
• Females who are pregnant or breastfeeding.
• Subject or caregiver unable to administer daily oral dosing of study drug.
• Participation in a non-Enterin investigational drug trial within the month prior to dosing in the present study.
• Any other reason, which in the opinion of the investigator would confound proper interpretation of the study.

Where it is running

• The Parkinson's and Movement Disorder Institute — Fountain Valley, California, United States
• SC3 Research - Pasadena — Pasadena, California, United States
• Rocky Mountain Movement Disorders Center — Englewood, Colorado, United States
• Georgetown Universtiy, Department of Neurology — Washington D.C., District of Columbia, United States
• JEM Research Institute — Atlantis, Florida, United States
• Parkinson's Disease and Movement Disorders Center of Boca Raton — Boca Raton, Florida, United States
• Parkinson's Disease Treatment Center of SWFL — Port Charlotte, Florida, United States
• Intercoastal Medical Group — Sarasota, Florida, United States
• USF Health Byrd Parkinson's Disease Movement Disorders Center of Excellence — Tampa, Florida, United States
• Premiere Research Institute at Palm Beach Neurology — West Palm Beach, Florida, United States
• Dartmouth Hitchcock Medical Center — Lebanon, New Hampshire, United States
• Albany Medical College — Albany, New York, United States
• Icahn School of Medicine at Mount Sinai — New York, New York, United States
• Cleveland Clinic — Cleveland, Ohio, United States
• University of Toledo Medical Center — Toledo, Ohio, United States
• Penn State University — Hershey, Pennsylvania, United States
• Evergreen Health - Booth Gardner Parkinson's Care Center — Kirkland, Washington, United States
• University Physicians & Surgeons, Inc. dba Marshall Health — Huntington, West Virginia, United States

Full record on ClinicalTrials.gov

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