A Safety and Efficacy Study of a Bowel Cleansing Preparation (BLI800) in Pediatric Subjects Undergoing Colonoscopy

The objective of this study is to compare the safety, tolerance and efficacy of BLI800 to a PEG based preparation prior to colonoscopy in adolescent patients.

Study Overview

• Status: Completed
• Conditions: Colonoscopy
• Intervention / Treatment: Drug: BLI800; Drug: PEG-ELS

• Study Type: Interventional
• Enrollment (Actual): 91
• Phase: Phase 3

Contacts and Locations

Study Locations

• United States
  • Alabama
    • Mobile, Alabama, United States, 36582
      • Braintree Research Site 27
  • Arizona
    • Tucson, Arizona, United States, 85724
      • Braintree Research Site 30
  • California
    • Orange, California, United States, 92868
      • Braintree Research Site 23
    • San Francisco, California, United States, 94158
      • Braintree Research Site 16
  • Florida
    • Gainesville, Florida, United States, 32610
      • Braintree Research Site 5
    • Jacksonville, Florida, United States, 32207
      • Braintree Research Site 24
    • Orlando, Florida, United States, 32806
      • Braintree Research Site 21
  • Georgia
    • Atlanta, Georgia, United States, 30342
      • Braintree Research Site 2
  • Illinois
    • Chicago, Illinois, United States, 60611
      • Braintree Research Site 13
    • Park Ridge, Illinois, United States, 60068
      • Braintree Research Site 3
  • Indiana
    • Indianapolis, Indiana, United States, 46202
      • Braintree Research Site 26
  • Minnesota
    • Minneapolis, Minnesota, United States, 55454
      • Braintree Research Site 25
    • Rochester, Minnesota, United States, 55905
      • Braintree Research Site 18
  • Mississippi
    • Flowood, Mississippi, United States, 39232
      • Braintree Research Site 1
  • New York
    • Bronx, New York, United States, 10467
      • Braintree Research Site 32
    • Buffalo, New York, United States, 14222
      • Braintree Research Site 9
    • New York, New York, United States, 10021
      • Braintree Research Site 28
    • New York, New York, United States, 10032
      • Braintree Research Site 19
  • Pennsylvania
    • Pittsburgh, Pennsylvania, United States, 15224
      • Braintree Research Site 6
  • Tennessee
    • Memphis, Tennessee, United States, 38103
      • Braintree Research Site 20
  • Texas
    • Plano, Texas, United States, 75093
      • Braintree Research Site 34
  • Utah
    • Salt Lake City, Utah, United States, 84118
      • Braintree Research Site 22
  • Vermont
    • Burlington, Vermont, United States, 05401
      • Braintree Research Site 10
  • Virginia
    • Norfolk, Virginia, United States, 23507
      • Braintree Research Site 17
    • Roanoke, Virginia, United States, 24013
      • Braintree Research Site 4
  • Washington
    • Seattle, Washington, United States, 98105
      • Braintree Research Site 11
  • Wisconsin
    • Milwaukee, Wisconsin, United States, 53226
      • Braintree Research Site 14

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 12 years to 16 years (CHILD)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Male or female between the ages of 12 to 16 (inclusive)

2. Undergoing colonoscopy for routinely accepted indications, including (but not limited to):

   • Subjected inflammatory bowel disease (IBD) or IBD follow-up
   • Lower gastrointestinal bleeding
   • Suspected colitis (allergic or other)
   • Abdominal pain
   • Chronic diarrhea
   • Cancer surveillance
   • Anemia of unknown etiology
   • Abnormal endosonography or manometry
   • Evaluation of barium enema results
3. If female, and of child-bearing potential, subject must use an acceptable form of birth control or remain abstinent for the duration of the study.
4. Negative pregnancy test at screening, if applicable
5. In the Investigator's judgment, caregiver is mentally competent to provide informed consent for their child to participate in the study.

Exclusion Criteria:

1. Subjects with known or suspected ileus, impaction, severe ulcerative colitis, acute peritonitis, gastrointestinal obstruction, gastric retention (gastroparesis), bowel perforation, toxic colitis or megacolon.
2. Subjects who had previous significant gastrointestinal surgeries.
3. Subjects with increased risk of bowel perforation, including connective tissue disorders, toxic dilation of the bowel or recent bowel surgery.
4. Subjects with uncontrolled pre-existing electrolyte abnormalities, or those with clinically significant electrolyte abnormalities based on Visit 1 laboratory results, such as hypernatremia, hyponatremia, hyperphosphatemia, hypokalemia, hypocalcemia, uncorrected dehydration, or those secondary to the use of diuretics or angiotensin converting enzyme (ACE) inhibitors.
5. Subjects with bleeding disorders and/or impaired platelet function, or neutropenia.
6. Subjects with a prior history of renal, liver or cardiac insufficiency (including congestive heart failure or other significant cardiac abnormality)
7. Subjects with estimated glomerular filtration rate (GFR) below normal range (less than 70 ml/min/1.73m2)
8. Subjects required to take any other oral medication within 3 hours of dosing until completion of both doses.
9. Subjects with impaired consciousness that predisposes them to pulmonary aspiration.
10. Subjects with tendency for nausea and/or vomiting, or that have known swallowing disorders.
11. Subjects for whom intake of substances is likely to affect gastrointestinal motility or urinary flow rate.
12. Subjects undergoing colonoscopy for foreign body removal and/or decompression.
13. Subjects with an abnormal ECG result at Visit 1.
14. Subjects who are pregnant or lactating, or intending to become pregnant during the study.
15. Subjects of childbearing potential who refuse a pregnancy test.
16. Subjects with a history of hypersensitivity to any preparation components.
17. Subjects who, in the opinion of the Investigator, should not be included in the study for any reason, including inability to follow study procedures and history of major medical/psychiatric conditions that would compromise the safety of the study.
18. Subjects who have participated in an investigational surgical, drug, or device study within the past 30 days.
19. Subjects who withdraw consent before completion of Visit 1 procedures.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: SINGLE

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: BLI800 high dose; BLI800 bowel preparation (high dose)	Drug: BLI800; BLI800 bowel preparation
EXPERIMENTAL: BLI800 low dose; BLI800 bowel preparation (low dose)	Drug: BLI800; BLI800 bowel preparation
ACTIVE_COMPARATOR: PEG-ELS; PEG based bowel preparation	Drug: PEG-ELS; polyethylene glycol based bowel preparation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number and Percentage of Subjects With Successful Bowel Cleansing	Cleansing is rated by a blinded colonoscopist on a 4 point scale (1=poor to 4 = excellent)	2 days

Collaborators and Investigators

• Sponsor: Braintree Laboratories

Study record dates

Study Major Dates

• Study Start: June 1, 2016
• Primary Completion (ACTUAL): March 27, 2018
• Study Completion (ACTUAL): March 27, 2018

Study Registration Dates

• First Submitted: June 28, 2016
• First Submitted That Met QC Criteria: June 28, 2016
• First Posted (ESTIMATE): June 30, 2016

Study Record Updates

• Last Update Posted (ACTUAL): May 3, 2021
• Last Update Submitted That Met QC Criteria: April 29, 2021
• Last Verified: April 1, 2021

More Information

Terms related to this study

• Other Study ID Numbers: BLI800-502

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO