Clinical Trials Study

Phase 4

Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Budesonide Extended-release Tablets in Pediatric Subjects Aged 5 to 17 Years With Active, Mild to Moderate Ulcerative Colitis

Conditions: Ulcerative Colitis

Study #:
NCT04314375
Last Updated:
09/16/2025
Recruitment Status:
Recruiting
Estimated Study Completion Date:
06/01/2027

Summary

This is a randomized, double-blind, placebo-controlled, multicenter, study to evaluate the efficacy, safety, and pharmacokinetics (PK) of budesonide extended-release tablets for the induction of remission in pediatric subjects, with active, mild to moderate ulcerative colitis (UC). Subjects will be permitted to continue taking background oral or rectal 5-aminosalicylate (5-ASA) products.

Age: 5 Years to 17 Years old

Gender: All

Start Date: 09/29/2023

Primary Completion Date (Estimated): 12/01/2026

Study Completion Date (Estimated): 06/01/2027

Accepts Healthy Volunteers: No

Trial Purpose and Description

Eligibility Criteria

Age: 5 Years to 17 Years old

Gender: All

Accepts Healthy Volunteers: No

Inclusion criteria:

* Established diagnosis of UC is based on:

* Clinical history

* Characteristic endoscopic findings

* Histopathology results from biopsies

* Age 5 to 17 years, inclusive, at Screening. Subjects should weigh greater than 13.6 kg at Baseline.

* Active UC of mild or moderate severity, defined as a total Mayo score between 4 and 10, inclusive, with rectal bleeding subscore of ≥ 1, stool frequency subscore of ≥1 and an endoscopy subscore of ≥ 1.

* If on a background oral or rectal 5-ASA, the dose and formulation have remained unchanged for at least 6 weeks prior to Visit 2 (randomization), Baseline and the subject is willing to remain on the same formulation and dose for the duration of the study.

Exclusion criteria:

1. Current or prior diagnosis of Crohn's disease or indeterminate colitis.

2. Limited distal proctitis (disease involving only the first 15 centimeters or less proximal to the anal verge.

3. Severe UC, defined as total Mayo score \>10.

4. Not currently in an active phase or flare, defined as a total Mayo score \<4, or Mayo score between 4 and 10, but Mayo subscore of 0 for rectal bleeding, stool frequency or endoscopy.

5. Infectious colitis (based on positive microbiologic tests at Screening) or any recent history of infectious colitis (within 30 days prior to Screening).

6. Prior gastrointestinal surgery, except appendectomy or hernia (e.g., inguinal, umbilical).

NOTE: Prior cholecystectomy is not exclusionary if more than 1 year prior to Screening.

7. Evidence or history of toxic megacolon or bowel resection.

Principal Investigator

Gitit Tomer, MD

For more information about this study, contact:

Gitit Tomer

718-741-2332

gitomer@montefiore.org