Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00780507
Other study ID # 2007096
Secondary ID
Status Completed
Phase Phase 3
First received October 24, 2008
Last updated May 29, 2013
Start date August 2007
Est. completion date July 2009

Study information

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

Clinical Trial Summary

The present study will analyze fecal levels of FC and FL in UC patients who relapse (flare) while on a QD or a BID Asacol treatment regimen and compare those levels to levels of FC and FL in UC patients who do not relapse (flare).


Recruitment information / eligibility

Status Completed
Enrollment 89
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:

- Be willing and able to provide written informed consent for this biomarker study;

- Be enrolled in Study 2007021 (QDIEM).

Exclusion Criteria:

- Meet the QDIEM Protocol 2007021 for Exclusion Criteria

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Research Facility Alexandria Virginia
United States Research Facility Anaheim California
United States Research Facility Arlington Heights Illinois
United States Research Facility Babylon New York
United States Research Facility Binghamton New York
United States Research Facility Boone North Carolina
United States Research Facility Bowling Green Kentucky
United States Research Facility Braintree Massachusetts
United States Research Facility Canton Ohio
United States Research Facility Cheektowaga New York
United States Research Facility Chesapeake Virginia
United States Research Facility Chesterfield Michigan
United States Research Facility Cincinnati Ohio
United States Research Facility Cincinnati Ohio
United States Research Facility Clive Iowa
United States Research Facility Decatur Georgia
United States Research Facility Egg Harbor Township New Jersey
United States Research Facility Folsom California
United States Research Facility Forest Hills New York
United States Research Facility Ft. Lauderdale Florida
United States Research Facility Greenville Texas
United States Research Facility Houston Texas
United States Research Facility Houston Texas
United States Research Facility Indiana Pennsylvania
United States Research Facility Jackson Tennessee
United States Research Facility Jefferson City Missouri
United States Research Facility Lafayette Colorado
United States Research Facility Lake Success New York
United States Research Facility Lancaster Pennsylvania
United States Research Facility Lewisville Texas
United States Research Facility Longview Texas
United States Research Facility Los Angeles California
United States Research Facility Lowell Arkansas
United States Research Facility Lutherville Maryland
United States Research Facility Marietta Georgia
United States Research Facility Merced California
United States Research Facility Morganton North Carolina
United States Research Facility New Bern North Carolina
United States Research Facility New Port Richey Florida
United States Research Facility Newnan Georgia
United States Research Facility Oak Lawn Illinois
United States Research Facility Odessa Texas
United States Research Facility Palm Harbor Florida
United States Research Facility Pasadena Texas
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 Raleigh North Carolina
United States Research Facility Rochester Hills Michigan
United States Research Facility San Diego California
United States Research Facility Shreveport Louisiana
United States Research Facility South Bend Indiana
United States Research Facility Spokane Washington
United States Research Facility Tampa Florida
United States Research Facility Topeka Kansas
United States Research Facility Torrington Connecticut
United States Research Facility Upland California
United States Research Facility Urbana Illinois
United States Research Facility Warwick Rhode Island
United States Research Facility Winchester Virginia
United States Research Facility Zephyrhills Florida

Sponsors (1)

Lead Sponsor Collaborator
Warner Chilcott

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compare the fecal biomarker calprotectin between the UC patients who relapse (flare) and the UC patients who remain in remission throughout the study while on Asacol regardless of the maintenance regimen. one year No
Secondary To compare the fecal levels of the 2 biomarkers (FC and FL) in patients who are on BID and QD treatment regimens and who remain in remission for the duration of the study; one year No
See also
  Status Clinical Trial Phase
Recruiting NCT05702879 - Combined Microbiota and Metabolic Signature in Ulcerative Colitis Predicts Anti-Inflammatory Therapy Success
Not yet recruiting NCT05953402 - A Study of Ozanimod in Pregnant Women With Ulcerative Colitis and Their Offspring
Recruiting NCT05316584 - A Novel Remote Patient and Medication Monitoring Solution to Improve Adherence and PerSiStence With IBD Therapy N/A
Recruiting NCT03950232 - An Extension Study for Treatment of Moderately to Severely Active Ulcerative Colitis Phase 3
Completed NCT03124121 - Study of the Golimumab Exposure-Response Relationship Using Serum Trough Levels Phase 4
Not yet recruiting NCT06100289 - A Study of Vedolizumab in Children and Teenagers With Ulcerative Colitis or Crohn's Disease Phase 3
Withdrawn NCT04209556 - A Study To Evaluate The Safety And Efficacy Of PF-06826647 In Participants With Moderate To Severe Ulcerative Colitis Phase 2
Terminated NCT00061282 - Clotrimazole Enemas for Pouchitis in Children and Adults Phase 1/Phase 2
Recruiting NCT04398550 - SCD vs. Mediterranean Diet Therapy in Ulcerative Colitis N/A
Recruiting NCT04314375 - Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Budesonide Extended-release Tablets in Pediatric Subjects Aged 5 to 17 Years With Active, Mild to Moderate Ulcerative Colitis Phase 4
Active, not recruiting NCT04857112 - Study Evaluating Efficacy and Safety of Amiselimod (MT-1303) in Mild to Moderate Ulcerative Colitis Phase 2
Completed NCT05051943 - A Study of the Real-world Use of an Adalimumab Biosimilar and Evaluation of Nutritional Status on the Therapeutic Response
Active, not recruiting NCT04033445 - A Study of Guselkumab in Participants With Moderately to Severely Active Ulcerative Colitis Phase 2/Phase 3
Recruiting NCT05428345 - A Study of Vedolizumab SC Given to Adults With Moderate to Severe Ulcerative Colitis or Crohn's Disease in South Korea
Active, not recruiting NCT06221995 - Energy Expenditure in Patients With Ulcerative Colitis Undergoing Surgery
Recruiting NCT04767984 - Testing Atorvastatin to Lower Colon Cancer Risk in Longstanding Ulcerative Colitis Phase 2
Completed NCT02508012 - Medico-economic Evaluation of the Therapeutic Drug Monitoring of Anti-TNF-α Agents in Inflammatory Bowel Diseases N/A
Recruiting NCT06071312 - FMT in Patients With Recurrent CDI and Ulcerative Colitis: Single Infusion Versus Sequential Approach Phase 1/Phase 2
Completed NCT03760003 - Dose-Ranging Phase 2b Study of ABX464 in Moderate to Severe Ulcerative Colitis Phase 2
Not yet recruiting NCT05539625 - Mini-MARVEL - Mitochondrial Antioxidant Therapy in Ulcerative Colitis Phase 2