Safety and Efficacy of MMX Mesalamine/Mesalazine in Pediatric Subjects With Mild to Moderate Ulcerative Colitis

Completed · Phase 3

Conditions studied: Ulcerative Colitis

In brief

To assess clinical response to MMX mesalamine/mesalazine between a low and high dose in children and adolescents aged 5-17 years with mild to moderate Ulcerative Colitis (UC) or who are in remission.

Key facts

Study ID

NCT02093663

Run by

Shire

People needed

107

Starts

2014-12-12

Expected to finish

2018-11-28

Last updated by the study team

2021-06-09

Who can join

Age: 5 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ability to voluntarily provide written, signed, and dated (personally or via a legally authorized representative [LAR]) informed consent or assent as applicable to participate in the study.
• Subject's parent/LAR demonstrates an understanding, ability, and willingness to fully comply with study procedures and restrictions.
• Male and female children and adolescents aged 5-17 years, inclusive.
• Body weight 18-90kg.
• Male, or non-pregnant, non-lactating female who agrees to comply with any applicable contraceptive requirements of the protocol or females of non-childbearing potential.
• Diagnosed with mild to moderate UC, established by sigmoidoscopy or colonoscopy with compatible histology. Screened subjects may also have an unconfirmed diagnosis of mild to moderate UC; however the diagnosis of mild to moderate UC must have been established by sigmoidoscopy or colonoscopy with compatible histology prior to baseline visit.
• Subject is able to swallow the investigational product whole.
• Double-blind Acute Phase:
• Partial UC-DAI score ≥2 (a combined rectal bleeding and stool frequency score ≥1 and PGA=1 or 2) at the Baseline Visit, for which 5-ASA would be used as part of normal treatment.
• If the subject is on 5-ASA treatment prior to study entry, then the dose must be stable. Stable therapy is defined as no change in dose, or no initiation of 5-ASA, from the onset of the current acute flare through discontinuation of therapy (required at the Baseline Visit).
• Double-blind Maintenance Phase:
• Partial UC-DAI ≤1 (rectal bleeding=0, stool frequency ≤1, and PGA=0) at the Baseline Visit.

You may not qualify if…

• Severe UC (defined by PGA=3).
• Crohn's disease, bleeding disorders, active peptic ulcer disease, or UC known to be confined to the rectum (isolated rectal proctitis).
• Asthma, only if known to be 5 ASA sensitive.
• Positive stool culture for enteric pathogens (including Salmonella, Shigella, Yersinia, Aeromonas, Plesiomonas, or Campylobacter). Clostridium difficile toxin, ova, or parasites present.
• Systemic or rectal corticosteroid use within 4 weeks prior to the Screening Visit. Topical, intranasal, or inhaled use is not exclusionary.
• Immunomodulator (6-mercaptopurine, azathioprine) use within 6 weeks prior to the Screening Visit.
• History of biologic (eg, anti-tumor necrosis factor agents, integrin receptor antagonists) use at any time.
• Antibiotic use within 7 days prior to the Screening Visit.
• Any anti-inflammatory drugs, not including 5-ASA treatment but including non-steroidal anti-inflammatory drugs such as aspirin, COX-2 inhibitors or ibuprofen, within 7 days prior to the Screening Visit unless used at over-the-counter levels for <3 days. However, prophylactic use of a stable dose of aspirin up to 325mg/day for cardiac disease is permitted.
• Prebiotic/probiotic use within 7 days prior to the Screening Visit. Yogurt products are permitted.

Where it is running

• University of Maryland Children's Hospital — Baltimore, Maryland, United States
• John Hopkins — Baltimore, Maryland, United States
• Massachusetts General Hospital — Boston, Massachusetts, United States
• Newton Wellesley Hospital — Newton, Massachusetts, United States
• University of Minnesota Children's Hospital — Minneapolis, Minnesota, United States
• Mayo Clinic Gastroenterology — Rochester, Minnesota, United States
• Penn State Milton S. Hershey Medical Center — Hershey, Pennsylvania, United States
• Texas Digestive Disease Consultants — Southlake, Texas, United States
• Carilion Medical Center — Roanoke, Virginia, United States
• University of Alberta Pediatric Gastroenterology & Nutrition — Edmonton, Alberta, Canada
• Szent Janos Korhaz És Észak-budai Egyesitett Korha — Budapest, Hungary
• Bekes Megyei Pandy Kalman Korhaz — Gyula, Hungary
• Baz Megyei Korhaz Es Egyetemi Oktatokorhaz — Miskolc, Hungary
• Szabolcs-Szatmar-Bereg Megyei Korhazak es Egyetemi Oktato Korhaz — Nyíregyháza, Hungary
• Szegedi Tudomanyegyetem Szent-Gyorgyi Albert Klinikai Kozpont — Szeged, Hungary
• Soroka Medical Center — Beersheba, Israel
• Rambam Health Corporation — Haifa, Israel
• Shaare Zedek Medical Center — Jerusalem, Israel
• Schneider Medical Centre — Petah Tikva, Israel
• Uniwersytecki Dzieciecy Szpital Kliniczny im. Ludwika Zamenhofa — Bialystok, Poland
• Klinika Pediatrii Gastroenterologii I Zywienia — Krakow, Poland
• Klinika Gastroenterologii I Pediatrii — Lodz, Poland
• Wojewodzki Specjalistyczny Szpital Dzieciecy — Olsztyn, Poland
• Gabinet Lekarski-Bartosz Korczowski — Rzeszów, Poland
• Oddzial Gastroenterologii I Hepatologii — Warsaw, Poland

Full record on ClinicalTrials.gov

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