Canadian Active & Maintenance Modified Pentasa Study

Last updated: April 21, 2016
Sponsor: Ferring Pharmaceuticals
Overall Status: Completed

Phase

3

Condition

Inflammatory Bowel Disease

Crohn's Disease

Treatment

N/A

Clinical Study ID

NCT00603733
CLN 35.3.11
  • Ages 18-75
  • All Genders

Study Summary

The purpose of this study is to demonstrate that the new modified oral extended-release Pentasa® 500mg tablet is at least as efficacious as the currently marketed Pentasa® 500mg tablet in active mild to moderate Ulcerative Colitis (UC) and also in maintenance of quiescent disease.

Eligibility Criteria

Inclusion

Inclusion Criteria for Active phase:

  • Newly diagnosed or recurrent, mild to moderate Ulcerative Colitis patients.

  • Extent of colonic involvement confirmed within the past 36 months

  • UCDAI score of at least 3 but not greater than 8 and a score of at least 1 forendoscopy

  • Screening tests to rule out any abnormalities in stool, heart or kidney.

  • Male or non-pregnant females between 18 to 75 years.

  • Women of childbearing potential to use efficacious contraception as judged by theinvestigator.

  • Written informed consent given. Inclusion Criteria for Maintenance phase:

  • Newly recruited subjects with documented mild to moderate UC entering the Run-inPhase: in clinical remission for at least 1 month and for a maximum of 3 years, andreceiving 5-ASA 1.4 to 2.5 g/day for maintenance of quiescent disease

  • Subjects from Active Phase: meeting remission criteria after the 8-week active period

  • Extent of colonic involvement confirmed within the past 36 months by colonoscopy

  • In complete remission at entry into the Maintenance Phase, defined as i) a score of 0or 1 for stool frequency; ii) a score of 0 for rectal bleeding; iii) a score of 0 forendoscopy findings; and iv) a Physician's Global Assessment (PGA) score of 0 or 1

  • Screening tests to rule out any abnormalities in stool, heart or kidney.

Exclusion

Exclusion Criteria:

  • Use of 5-ASA products at a dose >2.5g/day within 7 days prior to entry.

  • Proctitis, short bowel syndrome, prior bowel surgery, severe UC, other forms ofInflammatory Bowel Disease

  • Infectious diseases, parasites, bacterial pathogens

  • Allergy to aspirin or salicylate

  • Liver or kidney abnormalities

  • Alcohol or drug abuse

  • Pregnancy

  • Cancer

  • Bleeding disorders, ulcers, autoimmune diseases

  • Mental disorders

  • Participation in clinical trial in last 30 days

  • Inability to fill in diary cards / comply with protocol requirements

Study Design

Total Participants: 288
Study Start date:
October 01, 2007
Estimated Completion Date:
May 31, 2011

Study Description

A multi-centre, randomized, double-blind, non-inferiority trial comparing the efficacy and safety of a new modified oral extended release Pentasa® (mesalamine) 500 mg tablet to the currently marketed Pentasa® (mesalamine) 500 mg tablet in subjects with active mild to moderate ulcerative colitis treated with 4 g/day for 8 weeks and in maintenance of remission of ulcerative colitis in subjects treated with 2 g/day for 24 weeks. The study involves male or non-pregnant female subjects aged 18 to 75 years.

Subjects were randomised on entry into the trial, and if they were in remission at the end of the 8-week Active Phase or the 4-week Run-in Phase, they were eligible for enrolment into the 24-week Maintenance Phase, remaining on the original randomised treatment.

Connect with a study center

  • University of Calgary, Faculty of Medicine

    Calgary, Alberta
    Canada

    Site Not Available

  • Castledowns Medicentre

    Edmonton, Alberta
    Canada

    Site Not Available

  • Investigational site

    Brandon, Manitoba
    Canada

    Site Not Available

  • Hilyard Place Building A

    Saint John, New Brunswick
    Canada

    Site Not Available

  • Barrie GI Associates

    Barrie, Ontario
    Canada

    Site Not Available

  • Investigational site

    Guelph, Ontario
    Canada

    Site Not Available

  • St. Joseph's Healthcare

    Hamilton, Ontario
    Canada

    Site Not Available

  • Investigational site

    Oshawa, Ontario
    Canada

    Site Not Available

  • Investigational site - Phenix Building

    Ottawa, Ontario
    Canada

    Site Not Available

  • Ottawa General Hospital

    Ottawa, Ontario
    Canada

    Site Not Available

  • Digestive Health Clinic

    Richmond Hill, Ontario
    Canada

    Site Not Available

  • Investigational site

    Sarnia, Ontario
    Canada

    Site Not Available

  • Investigational site

    Sudbury, Ontario
    Canada

    Site Not Available

  • Investigational site

    Thunder Bay, Ontario
    Canada

    Site Not Available

  • JJ Dig Research Ltd

    Toronto, Ontario
    Canada

    Site Not Available

  • Keele Medical Place

    Toronto, Ontario
    Canada

    Site Not Available

  • St. Michael's Hospital

    Toronto, Ontario
    Canada

    Site Not Available

  • Toronto Digestive Disease Association (TDDA)

    Toronto, Ontario
    Canada

    Site Not Available

  • Hotel Dieu Grace Hospital

    Windsor, Ontario
    Canada

    Site Not Available

  • Investigational site

    Windsor, Ontario
    Canada

    Site Not Available

  • Investigational site

    Woodstock, Ontario
    Canada

    Site Not Available

  • Hotel Dieu de Levis

    Levis, Quebec
    Canada

    Site Not Available

  • Alpha Recherche Clinique Inc.

    Loretteville, Quebec
    Canada

    Site Not Available

  • Hopital Maissonneuve Rosemont

    Montreal, Quebec
    Canada

    Site Not Available

  • MUHC-Royal Victoria Hospital

    Montreal, Quebec
    Canada

    Site Not Available

  • Gastro Centre Hospitalier Universitaire de Québec/St-François-d'Assise Hospital

    Quebec,
    Canada

    Site Not Available

  • L'Hotel Dieu de Quebec

    Quebec,
    Canada

    Site Not Available

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