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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00505778
Other study ID # 2007021
Secondary ID
Status Completed
Phase Phase 3
First received July 20, 2007
Last updated April 15, 2013
Start date July 2007
Est. completion date July 2009

Study information

Verified date April 2013
Source Warner Chilcott
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the efficacy in maintaining remission of ulcerative colitis between a once daily (QD) Asacol regimen and a divided, twice daily (BID) Asacol dosing regimen.


Description:

Currently, in the US, Asacol therapy is indicated in divided doses for the maintenance of remission of ulcerative colitis at 1.6 g/day. A once daily dose is potentially beneficial to patients and physicians alike. This study will answer the following questions about once daily dosing: (1) does efficacy differ between once daily and twice daily dosing, (2) do patients prefer a once daily dosing regimen, and (3) is compliance better? This study will confirm whether there are benefits to once daily dosing beyond increased convenience. In order to understand how the QD regimen compares to BID in a "real life" practice setting, the patient will remain on the total daily dose of Asacol (1.6 g/day to 2.4 g/day) on which they were maintained in remission, but will be assigned to either a QD or BID regimen. This is an investigator-blinded study.


Recruitment information / eligibility

Status Completed
Enrollment 1027
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Documented history of ulcerative colitis that has been successfully maintained in remission for at least 3 months prior to study entry

- At least one flare in the past 18 months

- Utilizing a stable maintenance dose of oral Asacol of 1.6 g/day up to 2.4 g/day (stable dose is defined as the same dose for the past 3 months)

- Females must be postmenopausal or surgically sterile or have a negative urine pregnancy test and practice acceptable contraception

Exclusion Criteria:

- History of or current renal disease

- History of hepatic disease

- History of allergy or hypersensitivity to salicylates, aminosalicylates

- Treatment with immunomodulatory therapy, biologic therapy or corticosteroids within 90 days of screening

- Received any antidiarrheals, antispasmodics, or antibiotic within 1 month of screening

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Mesalamine Once-Daily
Mesalamine tablets, 1.6-2.4 g/day taken orally once a day for 52 weeks
Mesalamine Twice-Daily
Mesalamine tablets, 1.6-2.4 g/day, taken twice daily for 52 weeks

Locations

Country Name City State
Canada Research Facility Abbotsford British Columbia
Canada Research Facility Guelph Ontario
Canada Research Facility Hamilton Ontario
Canada Research Facility Montreal Quebec
Canada Research Facility Montreal Quebec
Canada Research Facility Ottawa Ontario
Canada Research Facility Quebec
Canada Research Facility Quebec
Canada Research Facility Toronto Ontario
Canada Research Facility Toronto Ontario
Puerto Rico Research Facility Ponce
Puerto Rico Research Facility San Juan
United States Research Facility Akron Ohio
United States Research Facility Albuquerque New Mexico
United States Research Facility Alexandria Louisiana
United States Research Facility Alexandria Virginia
United States Research Facility Allentown Pennsylvania
United States Research Facility Amarillo Texas
United States Research Facility Anaheim California
United States Research Facility Anderson Indiana
United States Research Facility Arlington Heights Illinois
United States Research Facility Athens Alabama
United States Research Facility Atlanta Georgia
United States Research Facility Aventura Florida
United States Research Facility Babylon New York
United States Research Facility Bangor Maine
United States Research Facility Beaver Falls Pennsylvania
United States Research Facility Berwyn Illinois
United States Research Facility Beverly Hills California
United States Research Facility Binghamton New York
United States Research Facility Birmingham Alabama
United States Research Facility Birmingham Alabama
United States Research Facility Bismarck North Dakota
United States Research Facility Bloomington Indiana
United States Research Facility Boise Idaho
United States Research Facility Boone North Carolina
United States Research Facility Boston Massachusetts
United States Research Facility Boston Massachusetts
United States Research Facility Bowling Green Kentucky
United States Research Facility Braintree Massachusetts
United States Research Facility Brooklyn New York
United States Research Facility Brooklyn New York
United States Research Facility Camden New Jersey
United States Research Facility Canton Ohio
United States Research Facility Cape Girardeau Missouri
United States Research Facility Cedar Knolls New Jersey
United States Research Facility Charlotte North Carolina
United States Research Facility Cheektowaga New York
United States Research Facility Chesapeake Virginia
United States Research Facility Chesterfield Michigan
United States Research Facility Chevy Chase Maryland
United States Research Facility Chicago Illinois
United States Research Facility Chico California
United States Research Facility Cincinnati Ohio
United States Research Facility Cincinnati Ohio
United States Research Facility Clairton Pennsylvania
United States Research Facility Cleveland Ohio
United States Research Facility Clive Iowa
United States Research Facility College Park Maryland
United States Research Facility Columbia Missouri
United States Research Facility Columbia South Carolina
United States Research Facility Columbia South Carolina
United States Research Facility Columbus Georgia
United States Research Facility Cortland New York
United States Research Facility Davenport Iowa
United States Research Facility Dayton Ohio
United States Research Facility Dayton Ohio
United States Research Facility Decatur Georgia
United States Research Facility Detroit Michigan
United States Research Facility Dothan Alabama
United States Research Facility Egg Harbor Township New Jersey
United States Research Facility Elgin Illinois
United States Research Facility Encinitas California
United States Research Facility Englewood Colorado
United States Research Facility Fairfax Virginia
United States Research Facility Folsum California
United States Research Facility Forest Hills New York
United States Research Facility Fort Lauderdale Florida
United States Research Facility Fort Worth Texas
United States Research Facility Gainesville Florida
United States Research Facility Garden City New York
United States Research Facility Golden Colorado
United States Research Facility Great Neck New York
United States Research Facility Great Neck New York
United States Research Facility Greenbelt Maryland
United States Research Facility Greensboro North Carolina
United States Research Facility Greenville North Carolina
United States Research Facility Greenville Texas
United States Research Facility Greer South Carolina
United States Research Site Hackensack New Jersey
United States Research Facility Hagerstown Maryland
United States Research Facility Hartford Connecticut
United States Research Facility Highland Park Illinois
United States Research Facility Hoffman Estates Illinois
United States Research Facility Hollywood Florida
United States Research Facility Hollywood Maryland
United States Research Facility Homewood Illinois
United States Research Facility Houston Texas
United States Research Facility Houston Texas
United States Research Facility Houston Texas
United States Research Facility Idaho Falls Idaho
United States Research Facility Indiana Pennsylvania
United States Research Facility Indianapolis Indiana
United States Research Facility Indianapolis Indiana
United States Research Facility Jackson Tennessee
United States Research Facility Jackson Tennessee
United States Research Facility Jacksonville North Carolina
United States Research Facility Jacksonville Florida
United States Research Facility Jacksonville Florida
United States Research Facility Jefferson City Missouri
United States Research Facility Kalamazoo Michigan
United States Research Facility Kinston North Carolina
United States Research Facility La Mesa California
United States Research Facility Lafayette Colorado
United States Research Facility Lafayette Louisiana
United States Research Facility Lake Barrington Illinois
United States Research Facility Lake Success New York
United States Research Facility Lancaster California
United States Research Facility Lancaster Pennsylvania
United States Research Facility Largo Florida
United States Research Facility Las Vegas Nevada
United States Research Facility Lewisville Texas
United States Research Facility Little Rock Arkansas
United States Research Facility Long Beach California
United States Research Facility Longview Texas
United States Research Facility Los Angeles California
United States Research Facility Los Angeles California
United States Research Facility Louisville Kentucky
United States Research Facility Louisville Kentucky
United States Research Facility Lowell Arkansas
United States Research Facility Lutherville Maryland
United States Research Facility Madera California
United States Research Facility Maitland Florida
United States Research Facility Marietta Georgia
United States Research Facility Marietta Georgia
United States Research Facility Memphis Tennessee
United States Research Facility Mentor Ohio
United States Research Facility Merced California
United States Research Facility Meriden Connecticut
United States Research Facility Metairie Louisiana
United States Research Facility Mexico Missouri
United States Research Facility Milwaukee Wisconsin
United States Research Facility Mission Hills California
United States Research Facility Monroe Louisiana
United States Research Facility Monroe Wisconsin
United States Research Facility Monterey California
United States Research Facility Morganton North Carolina
United States Research Facility Morristown Tennessee
United States Research Facility Mt Airy North Carolina
United States Research Facility Murrieta California
United States Research Facility Naples Florida
United States Research Facility New Haven Connecticut
United States Research Facility New Port Richey Florida
United States Research Facility New York New York
United States Research Facility New York New York
United States Research Facility Newbern North Carolina
United States Research Facility Newnan Georgia
United States Research Facility Norfolk Virginia
United States Research Facility North Miami Beach Florida
United States Research Facility Norwalk Connecticut
United States Research Facility Oak Lawn Illinois
United States Research Facility Oakland California
United States Research Facility Ocean New Jersey
United States Research Facility Odessa Texas
United States Research Facility Ogden Utah
United States Research Facility Orange California
United States Research Facility Orlando Florida
United States Research Facility Palm Harbor Florida
United States Research Facility Palm Springs California
United States Research Facility Pasadena Texas
United States Research Facility Peoria Illinois
United States Research Facility Philadelphia Pennsylvania
United States Research Facility Phoenix Arizona
United States Research Facility Phoenixville Pennsylvania
United States Research Facility Pinehurst North Carolina
United States Research Facility Pittsburgh Pennsylvania
United States Research Facility Pittsburgh Pennsylvania
United States Research Facility Pittsford New York
United States Research Facility Plano Texas
United States Research Facility Port Jefferson Station New York
United States Research Facility Port Orange Florida
United States Research Facility Portland Oregon
United States Research Facility Pratt Kansas
United States Research Facility Pueblo Colorado
United States Research Facility Raleigh North Carolina
United States Research Facility Reisterstown Maryland
United States Research Facility Rochester Minnesota
United States Research Facility Rochester New York
United States Research Facility Rochester New York
United States Research Facility Rockville Maryland
United States Research Facility Rockville Maryland
United States Research Facility Salt Lake City Utah
United States Research Facility San Antonio Texas
United States Research Facility San Carlos California
United States Research Facility San Diego California
United States Research Facility San Diego California
United States Research Facility San Diego California
United States Research Facility San Francisco California
United States Research Facility San Francisco California
United States Research Facility Savannah Georgia
United States Research Facility Scottsdale Arizona
United States Research Facility Seattle Washington
United States Research Facility Sewickley Pennsylvania
United States Research Facility Shreveport Louisiana
United States Research Facility Somersworth New Hampshire
United States Research Facility Souderton Pennsylvania
United States Research Facility South Bend Indiana
United States Research Facility South Plainfield New Jersey
United States Research Facility Southbridge Massachusetts
United States Research Facility Spokane Washington
United States Research Facility St Louis Missouri
United States Research Facility St Petersburg Florida
United States Research Facility St. Petersburg Florida
United States Research Facility Tacoma Washington
United States Research Facility Tallahassee Florida
United States Research Facility Tampa Florida
United States Research Facility Tampa Florida
United States Research Facility Toledo Ohio
United States Research Facility Topeka Kansas
United States Research Facility Torrance California
United States Research Facility Torrance California
United States Research Facility Torrington Connecticut
United States Research Facility Trinity Florida
United States Research Facility Troy Michigan
United States Research Facility Tucson Arizona
United States Research Facility Tulsa Oklahoma
United States Research Facility Tupelo Mississippi
United States Research Facility Tuscon Arizona
United States Research Facility Uniontown Pennsylvania
United States Research Facility Upland California
United States Research Facility Urbana Illinois
United States Research Facility Virginia Beach Virginia
United States Research Facility Warwick Rhode Island
United States Research Facility Washington District of Columbia
United States Research Facility Waterloo Iowa
United States Research Facility Wenatchee Washington
United States Research Facility West Bloomfied Michigan
United States Research Facility West Valley City Utah
United States Research Facility Westlake Ohio
United States Research Site Whichita Kansas
United States Research Facility Wilmington North Carolina
United States Research Facility Winchester Virginia
United States Research Facility Winter Park Florida
United States Research Facility Wyoming Michigan
United States Research Facility Zephyrhills Florida

Sponsors (1)

Lead Sponsor Collaborator
Warner Chilcott

Countries where clinical trial is conducted

United States,  Canada,  Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Patients Remaining in Remission at Month 6, ITT Population, Determined by the Simple Clinical Colitis Activity Index (SCCAI) Remission defined as SCCAI <5. Simple Clinical Colitis Activity Index: minimum score 0, maximum score 19, reflects disease activity over the 24 hours prior to completion. Composite Score: bowel frequency (day, 0-3) (night, 0-2), defecation urgency (0-3), blood in stool (0-3), general well being (0-4), extracolonic features (arthritis, pyoderma gangrenosum, erythema nodosum, uveitis - 1 per manifestation). 6 months Yes
Secondary Percentage of Patients Remaining in Remission at Month 3, ITT Population Remission defined as SCCAI < 5. Simple Clinical Colitis Activity Index: minimum score 0, maximum score 19, reflects disease activity over the 24 hours prior to completion. Composite Score: bowel frequency (day, 0-3) (night, 0-2), defecation urgency (0-3), blood in stool (0-3), general well being (0-4), extracolonic features (arthritis, pyoderma gangrenosum, erythema nodosum, uveitis - 1 per manifestation). 3 months No
Secondary Percentage of Patients Remaining in Remission at Month 12, ITT Population Remission defined as SCCAI score < 5. Simple Clinical Colitis Activity Index: minimum score 0, maximum score 19, reflects disease activity over the 24 hours prior to completion. Composite Score: bowel frequency (day, 0-3) (night, 0-2), defecation urgency (0-3), blood in stool (0-3), general well being (0-4), extracolonic features (arthritis, pyoderma gangrenosum, erythema nodosum, uveitis - 1 per manifestation). 12 months No
Secondary Number of Subjects Who Relapse/Flare Within 6 Months, ITT Population Relapse/flare is defined as SCCAI >= 5. Simple Clinical Colitis Activity Index: minimum score 0, maximum score 19, reflects disease activity over the 24 hours prior to completion. Composite Score: bowel frequency (day, 0-3) (night, 0-2), defecation urgency (0-3), blood in stool (0-3), general well being (0-4), extracolonic features (arthritis, pyoderma gangrenosum, erythema nodosum, uveitis - 1 per manifestation). 6 months Yes
Secondary Total MARS (Medication Adherence Report Scale) Questionnaire Scores, ITT Population, Month 6 MARS: Composite score for the following statements: I change how many times per day I take my medicine, I forget to use it, I stop taking it for a while, I only use it when I am having active symptoms, I decide to miss out on a dose, I take less than instructed, I take more than instructed, I avoid using it if I can, I use it regularly every day (reverse scored): 5-never, 4-rarely, 3-sometimes, 2-often, 1-very often. Minimum score 9, maximum score 45. 6 months No
Secondary Percentage of Participants Indicating Ulcerative Colitis in Remission (Patient Defined Remission Index), ITT Population, Month 6 Is your ulcerative colitis in remission (not active)? Y/N 6 months No
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