An Efficacy and Safety Study of Omega-3 Free Fatty Acids (Epanova™) for the Maintenance of Symptomatic Remission in Subjects With Crohn's Disease

Last updated: February 20, 2007
Sponsor: Tillotts Pharma AG
Overall Status: Completed

Phase

3

Condition

Crohn's Disease

Ulcerative Colitis

Colic

Treatment

N/A

Clinical Study ID

NCT00074542
Protocol TP0308 (EPIC-2)
  • Ages > 16
  • All Genders

Study Summary

The purpose of this study is to see if Epanova™ is able to maintain the symptomatic remission in subjects with Crohn's Disease who are responding to steroid induction therapy.

Patient safety and quality of life will also be monitored throughout the study.

Eligibility Criteria

Inclusion

Key Inclusion Criteria:

  • symptomatic active Crohn's disease (requiring a 16-week course of induction steroidtherapy at a starting dose of prednisone 40 mg or budesonide 9 mg daily)

  • respond to induction therapy (CDAI<150) following 8 weeks of steroid tapering regimento prednisone 20 mg or budesonide 6 mg daily

  • Crohn's disease of at least 3 months duration

  • 16 years of age or older

Exclusion

Key Exclusion Criteria:

  • intolerance of omega-3 free fatty acid (FFA)

  • intolerance of both prednisone and budesonide

  • ongoing therapy for Crohn's disease with: 5-ASA compounds, immune modifiers, systemicantibiotics, tube feeding

  • received in the past 3 months: systemic steroid therapy (other than study prednisoneor budesonide induction therapy), azathioprine, 6-mercaptopurine, methotrexate,cyclosporine, probiotic products, preparations containing omega-3 fatty acids

  • received in the past 6 months: biologicals e.g. enbrel, infliximab, monoclonalantibody, mycophenolate, tacrolimus, thalidomide, other immune modifiers and/orinvestigational products

  • chronic narcotic analgesics for pain control

  • short bowel syndrome, ostomy or need for bowel surgery for Crohn's disease, bowelobstruction or resection in the past 3 months

  • malignancy, clinically significant impairment or conditions which could interfere withthe evaluation of the trial medication

  • clinically relevant hematology, liver and renal function laboratory tests

  • known allergy to fish or fish products

Study Design

Total Participants: 364
Study Start date:
September 01, 2002
Estimated Completion Date:
January 31, 2005

Study Description

Crohn's disease is a chronic inflammatory disorder that frequently involves the colon and small bowel. Patients commonly experience abdominal pain, diarrhea, and malaise which result in decreased quality of life and an increased risk of chronic disability and unemployment.

Currently available therapeutic options for the maintenance of remission in Crohn's disease are inadequate. Patients' quality of life is often severely diminished. A clear need exists for well-tolerated drugs that can reliably reduce the risk of a disease relapse.

In recent years considerable attention has been focused on dietary marine fish oils as a means of treating several chronic inflammatory disorders including Crohn's disease. Fish oils have been found to reduce the inflammation and the severity of lesions in animal models of inflammatory bowel disease.

Commercially available fish oils are supplied as fatty acid triglycerides or ethyl esters and are often associated with unpleasant side effects such as nausea, flatulence, diarrhea and belching. These adverse effects limit administration of high doses of these preparations. Several studies have demonstrated the superior absorption across intestinal membranes of free fatty acids in comparison with triglycerides and ethyl esters. Epanova™ is being developed as a well-tolerated means of delivering a high concentration of marine fish oils as free fatty acids. Additionally, the gelatin coating of the capsules consists of a permeable polymer that results in a delayed release of the active compounds thus reducing the frequency of adverse events.

The objectives of this clinical trial are as follows:

Primary Objective:

  • To assess the ability of Epanova™ to maintain symptomatic remission in subjects with Crohn's Disease who are responding to steroid induction therapy

Secondary objectives:

  • To assess the safety and tolerability of Epanova™

  • To assess the ability of Epanova™ to maintain the quality of life in subjects with Crohn’s Disease who are responding to steroid induction therapy

  • To assess the efficacy of Epanova™ by Crohn’s Disease Activity Index (CDAI), Investigator and Subject Global Ratings, employment status and use of Crohn’s Disease related medical visits in subjects with Crohn’s Disease who are responding to steroid induction therapy

Connect with a study center

  • Health Sciences Centre

    Calgary, Alberta T1Y 6J4
    Canada

    Site Not Available

  • Royal Alexandra Hospital

    Edmonton, Alberta T5H 4B9
    Canada

    Site Not Available

  • University of Alberta

    Edmonton, Alberta T6G 2C8
    Canada

    Site Not Available

  • St. Paul's Hospital

    Vancouver, British Columbia V6Z 1Y6
    Canada

    Site Not Available

  • Vancouver General Hospital

    Vancouver, British Columbia V5Z 1L5
    Canada

    Site Not Available

  • Health Sciences Centre

    Winnipeg, Manitoba R3A 1R9
    Canada

    Site Not Available

  • Victoria General Hospital

    Halifax, Nova Scotia B3H 1V7
    Canada

    Site Not Available

  • London Health Sciences Centre (South Street Campus)

    London, Ontario N6A 4G5
    Canada

    Site Not Available

  • London Health Sciences Centre (University Campus)

    London, Ontario N6A 5A5
    Canada

    Site Not Available

  • The Ottawa Hospital (Civic Campus)

    Ottawa, Ontario K1Y 4E9
    Canada

    Site Not Available

  • Mount Sinai Hospital

    Toronto, Ontario M5G 1X5
    Canada

    Site Not Available

  • St. Michael's Hospital

    Toronto, Ontario M5B 1W8
    Canada

    Site Not Available

  • Sunnybrook & Women's College HSC

    Toronto, Ontario M4N 3M5
    Canada

    Site Not Available

  • CHUQ - Pavillon St-François d'Assise

    Montreal, Quebec G1L 3L5
    Canada

    Site Not Available

  • Hopital Maisonneuve-Rosemont

    Montreal, Quebec H1T 2M4
    Canada

    Site Not Available

  • Hôpital Saint-Luc

    Montreal, Quebec H2X 3J4
    Canada

    Site Not Available

  • Jewish General Hospital

    Montreal, Quebec H3T 1E2
    Canada

    Site Not Available

  • Montreal General Hospital

    Montreal, Quebec H3G 1A4
    Canada

    Site Not Available

  • Royal Victoria Hospital

    Montreal, Quebec H3A 1A1
    Canada

    Site Not Available

  • CHUQ-Hôtel-Dieu de Québec

    Québec, Quebec G1R 2J6
    Canada

    Site Not Available

  • CHUQ-Hôtel-Dieu de Québec

    Québec, Quebec G1R 2J6
    Canada

    Site Not Available

  • Hôpital St-Sacrement

    Quebec, G1S 4L8
    Canada

    Site Not Available

  • Atlanta Gastroenterology Associates

    Atlanta, Georgia 30342-5006
    United States

    Site Not Available

  • Northwestern University Medical School

    Chicago, Illinois 60611
    United States

    Site Not Available

  • University of Chicago Medical Center

    Chicago, Illinois 60637
    United States

    Site Not Available

  • Carle Clinic Association

    Urbana, Illinois 61801
    United States

    Site Not Available

  • University of Louisville, Department of Surgery

    Louisville, Kentucky 40292
    United States

    Site Not Available

  • Mayo Clinic

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Gastroenterology Specialties, P.C.

    Lincoln, Nebraska 68503
    United States

    Site Not Available

  • Long Island Clinical Research Associates

    Great Neck, New York 11021
    United States

    Site Not Available

  • University of North Carolina Chapel Hill

    Chapel Hill, North Carolina 27599-7032
    United States

    Site Not Available

  • Cleveland Clinic Foundation

    Cleveland, Ohio 44195
    United States

    Site Not Available

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