Actively Recruiting
4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 Yrs
Led by Ardelyx · Updated on 2026-05-12
72
Participants Needed
20
Research Sites
96 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a randomized, double-blind, placebo-controlled dose-ranging study to assess the safety and efficacy of tenapanor for treatment of the IBS-C in pediatric patients 6 to less than 12 year old.
CONDITIONS
Official Title
4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 Yrs
Who Can Participate
Eligibility Criteria
You may qualify if you...
- ≥6 and <12 years old at the Screening visit (Visit 1)
- Confirmation of negative pregnancy test and use of appropriate contraceptive (including abstinence) in female subjects that have experienced menarche and are of child-bearing potential.
- Meet the Modified Diagnostic Rome IV criteria for child/adolescent diagnosis of IBS-C
- Patient is willing to discontinue any laxatives used in favor of the protocol-permitted rescue medicine (which will only be allowed after 72 hours with no bowel movement)
- Meet the entry criteria assessed during the 2-week Screening period
- Ability of both the patient and parent/guardian/LAR to communicate with the Investigator and to comply with the requirements of the entire study, including an understanding of the assessments in the eDiary and how to use the eDiary device
- Patient must provide verbal assent and the parent/guardian/LAR must provide written informed consent before the initiation of any study-specific procedures
You will not qualify if you...
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Functional diarrhea as defined by Modified Rome IV child/adolescent criteria
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IBS with diarrhea (IBS-D), mixed IBS (IBS-M), or unsubtyped IBS as defined by Modified Rome IV child/adolescent criteria
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History of non-retentive fecal incontinence;
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Required manual disimpaction any time prior to randomization (after consent)
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Currently has both unexplained and clinically significant alarm symptoms (lower gastrointestinal [GI] bleeding [rectal bleeding or heme-positive stool], iron-deficiency anemia, or any unexplained anemia, or weight loss) and systemic signs of infection or colitis, or any neoplastic process.
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Patient has any of the following conditions:
- Celiac disease, or positive serological test for celiac disease and the condition has not been ruled out by endoscopic biopsy;
- Cystic fibrosis;
- Hypothyroidism that is untreated or treated with thyroid hormone at a dose that has not been stable for at least 3 months prior to the Screening Visit;
- Down's syndrome or any other chromosomal disorder;
- Active anal fissure (Note: History of anal fissure is not an exclusion);
- Anatomic malformations (eg, imperforate anus, anal stenosis, anterior displaced anus);
- Intestinal nerve or muscle disorders (eg, Hirschprung disease, visceral myopathies, visceral neuropathies);
- Neuropathic conditions (eg, spinal cord abnormalities, neurofibromatosis, tethered cord, spinal cord trauma);
- Lead toxicity, hypercalcemia;
- Neurodevelopmental disabilities
- Inflammatory bowel disease
- Childhood functional abdominal pain syndrome
- Childhood functional abdominal pain
- Poorly treated or poorly controlled psychiatric disorders that might influence his or her ability to participate in the study;
- Lactose intolerance that is associated with abdominal pain or discomfort and could confound the assessments in this study
- History of cancer other than treated basal cell carcinoma of the skin;
- History of diabetic neuropathy.
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Use of medications that are known to affect stool consistency (Prohibited Medications), including fiber supplements, anti-diarrheals, cathartics, antacids, opiates, prokinetic drugs, laxatives, enemas, antibiotics during the Screening period; unless specified as rescue medication, and used accordingly as directed by the Investigator.
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Patient has had surgery that meets any of the following criteria:
- Surgery to remove a segment of the GI tract at any time before the Screening Visit;
- Surgery of the abdomen, pelvis, or retroperitoneal structures during the 6 months before the Screening Visit;
- An appendectomy or cholecystectomy during the 60 days before the Screening Visit;
- Other major surgery during the 30 days before the Screening Visit
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History of alcohol or substance abuse
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Participation in other clinical trials within 1 month prior to Screening
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Patient and/or parent/guardian/LAR is involved in the conduct and/or administration of this trial as an investigator, sub-investigator, trial coordinator, or other staff member, or the patient is a first-degree family member, significant other, or relative residing with one of the above persons involved in the trial
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If, in the opinion of the Investigator, the patient is unable or unwilling to fulfill the requirements of the protocol or has a condition, which would render the results uninterpretable
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 20 locations
1
Applied Research Center of Arkansas
Little Rock, Arkansas, United States, 72205
Actively Recruiting
2
Connecticut Children's Medical Center
Hartford, Connecticut, United States, 06106
Actively Recruiting
3
Waterway Research & Associates Corp.
Miami, Florida, United States, 33155
Actively Recruiting
4
Valencia Medical and Research Center
Miami, Florida, United States, 33165
Actively Recruiting
5
Orlando Health, Inc.- APH Center for Digestive Health and Nutrition
Orlando, Florida, United States, 32806
Actively Recruiting
6
Florida Pharmaceutical Research and Associates, Inc.
South Miami, Florida, United States, 33143
Actively Recruiting
7
OSF Saint Francis Medical Center
Peoria, Illinois, United States, 61637
Actively Recruiting
8
Mankato Clinic Children's Health Center
Mankato, Minnesota, United States, 56001
Actively Recruiting
9
Boys Town National Research Hospital
Boys Town, Nebraska, United States, 68010
Actively Recruiting
10
SUNY Downstate Medical Center
Brooklyn, New York, United States, 11203
Actively Recruiting
11
Wilmington Health
Wilmington, North Carolina, United States, 28401
Actively Recruiting
12
Akron Children's Hospital
Akron, Ohio, United States, 44308
Actively Recruiting
13
Prisma Health Children's Hospital
Greenville, South Carolina, United States, 29615
Actively Recruiting
14
Maspons Pediatric Gastro
El Paso, Texas, United States, 79902
Actively Recruiting
15
Proactive El Paso, LLC
El Paso, Texas, United States, 79902
Actively Recruiting
16
Texas Digestive Specialists
Harlingen, Texas, United States, 78550
Actively Recruiting
17
Sun Research Institute
San Antonio, Texas, United States, 78215
Actively Recruiting
18
Pioneer Research Solutions Inc
Sugar Land, Texas, United States, 77479
Actively Recruiting
19
Clinical Research Partners, LLC
Richmond, Virginia, United States, 23226
Actively Recruiting
20
University Physicians and Surgeons, Inc
Huntington, West Virginia, United States, 25701
Actively Recruiting
Research Team
S
Shannon Song
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
7
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