Ulcerative colitis (UC) is a type of inflammatory bowel disease (IBD) characterized by diffuse, continuous inflammation of the colon. This study will assess how safe and effective mesalamine delayed-release capsules are in treating pediatric participants with UC. Adverse events and change in disease activity will be assessed. Delzicol (Mesalamine) is an approved drug being developed for the treatment of Ulcerative Colitis (UC). Study doctors put the participants in 1 of 2 groups, called treatment arms. Each group receives a different treatment. Around 80 Pediatric participants aged 5 to 17 years with a diagnosis of UC will be enrolled in approximately 45 sites in the United States. Participants will receive oral mesalamine capsules twice daily for 26 weeks and followed for 30 days. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Oral Capsules
Oral Capsule
Childrens National /ID# 243379
Washington D.C., District of Columbia, United States
Angel Kids Pediatrics /ID# 244874
Jacksonville, Florida, United States
Treken Primary Care /ID# 241302
Atlanta, Georgia, United States
Eagle Clinical Research /ID# 242045
Chicago, Illinois, United States
Virgo Carter Pediatrics /ID# 241556
Silver Spring, Maryland, United States
UH Cleveland Medical Center /ID# 243375
Cleveland, Ohio, United States
Children's Hospital Oklahoma /ID# 242614
Oklahoma City, Oklahoma, United States
Carilion Medical Center /ID# 244398
Roanoke, Virginia, United States
San Juan Bautista School of Medicine /ID# 243377
Caguas, Puerto Rico
Centro de Investigaciones Clinicas San Jorge Children's and Women's Hospital /ID# 244595
San Juan, Puerto Rico
Percentage of Participants Maintaining Clinical Remission Responder Status Based on the modified Mayo Score (mMS)
Clinical remission responder based on the mMS is defined as Endoscopy subscore = 0 or 1, AND Rectal bleeding subscore = 0, AND Stool frequency subscore \<= 1.
Time frame: Week 26
Percentage of Participants Maintaining Endoscopic Remission Responder Status Based on the mMS
Endoscopic remission responder based on the mMS is defined as Endoscopy subscore = 0 or 1.
Time frame: Week 26
Percentage of Participants Maintaining Symptomatic Remission Responder Status Based on the mMS
Symptomatic remission responder based on the mMS s defined as Rectal bleeding subscore = 0 AND Stool frequency subscore \<= 1.
Time frame: Week 26
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