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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01130272
Other study ID # 27018966IBS2001
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date April 28, 2010
Est. completion date July 14, 2011

Study information

Verified date September 2019
Source Furiex Pharmaceuticals, Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the efficacy, safety, and tolerability of different doses of JNJ-27018966 (eluxadoline) compared with placebo in the treatment of patients with irritable bowel syndrome with diarrhea (IBS-d).


Recruitment information / eligibility

Status Completed
Enrollment 807
Est. completion date July 14, 2011
Est. primary completion date July 14, 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Key Inclusion Criteria:

- Patient has a diagnosis of IBS by Rome III criteria with a subtype of diarrhea

- Female patients must be:

- postmenopausal, defined as amenorrhea for at least 2 years at Prescreening,

- surgically sterile (have had a hysterectomy or bilateral oophorectomy, tubal ligation, or otherwise be incapable of pregnancy),

- abstinent, or

- if sexually active, be practicing an effective method of birth control.

Key Exclusion Criteria:

- Patient has a diagnosis of IBS by Rome III criteria with a subtype of constipation, mixed IBS, or unsubtyped IBS

- Patient has a history of inflammatory or immune-mediated gastrointestinal (GI) disorders including inflammatory bowel disease (ie, Crohn's disease, ulcerative colitis) and celiac disease

- Patient has a history of diverticulitis within 6 months prior to Prescreening

- Patient has a history of intestinal obstruction, stricture, toxic megacolon, GI perforation, fecal impaction, gastric banding, bariatric surgery, adhesions, ischemic colitis, impaired intestinal circulation (eg, aortoiliac disease), thrombophlebitis of a major vein, or hypercoagulable states.

Other protocol-specific eligibility criteria may apply.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Eluxadoline
Tablets, orally, twice daily.
Placebo
Matching placebo oral tablets twice daily.

Locations

Country Name City State
United States Furiex Research Site Akron Ohio
United States Furiex Research Site Albuquerque New Mexico
United States Furiex Research Site Albuquerque New Mexico
United States Furiex Research Site Alexandria Virginia
United States Furiex Research Site Aliso Viejo California
United States Furiex Research Site Anaheim California
United States Furiex Research Site Anderson Indiana
United States Furiex Research Site Anderson South Carolina
United States Furiex Research Site Annapolis Maryland
United States Furiex Research Site Anniston Alabama
United States Furiex Research Site Atco New Jersey
United States Furiex Research Site Atlanta Georgia
United States Furiex Research Site Atlanta Georgia
United States Furiex Research Site Austin Texas
United States Furiex Research Site Aventura Florida
United States Furiex Research Site Azusa California
United States Furiex Research Site Beachwood Ohio
United States Furiex Research Site Beavercreek Ohio
United States Furiex Research Site Bedford Texas
United States Furiex Research Site Bellevue Nebraska
United States Furiex Research Site Billings Montana
United States Furiex Research Site Binghamton New York
United States Furiex Research Site Birmingham Alabama
United States Furiex Research Site Birmingham Alabama
United States Furiex Research Site Blackwood New Jersey
United States Furiex Research Site Bloomington Indiana
United States Furiex Research Site Boca Raton Florida
United States Furiex Research Site Boca Raton Florida
United States Furiex Research Site Boise Idaho
United States Furiex Research Site Boise Idaho
United States Furiex Research Site Boone North Carolina
United States Furiex Research Site Boston Massachusetts
United States Furiex Research Site Boston Massachusetts
United States Furiex Research Site Boston Massachusetts
United States Furiex Research Site Bowling Green Kentucky
United States Furiex Research Site Bozeman Montana
United States Furiex Research Site Bradenton Florida
United States Furiex Research Site Brandon Florida
United States Furiex Research Site Bristol Connecticut
United States Furiex Research Site Bristol Tennessee
United States Furiex Research Site Brockton Massachusetts
United States Furiex Research Site Brooklyn New York
United States Furiex Research Site Brooklyn New York
United States Furiex Research Site Burbank California
United States Furiex Research Site Carlsbad California
United States Furiex Research Site Champaign Illinois
United States Furiex Research Site Chandler Arizona
United States Furiex Research Site Chapel Hill North Carolina
United States Furiex Research Site Charlotte North Carolina
United States Furiex Research Site Charlotte North Carolina
United States Furiex Research Site Chaska Minnesota
United States Furiex Research Site Chattanooga Tennessee
United States Furiex Research Site Chattanooga Tennessee
United States Furiex Research Site Chesapeake Virginia
United States Furiex Research Site Chesterfield Michigan
United States Furiex Research Site Chevy Chase Maryland
United States Furiex Research Site Chicago Illinois
United States Furiex Research Site Chipley Florida
United States Furiex Research Site Christiansburg Virginia
United States Furiex Research Site Cincinnati Ohio
United States Furiex Research Site Cleveland Ohio
United States Furiex Research Site Colleyville Texas
United States Furiex Research Site Colorado Springs Colorado
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United States Furiex Research Site Dingmans Ferry Pennsylvania
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United States Furiex Research Site Dothan Alabama
United States Furiex Research Site Duluth Georgia
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United States Furiex Research Site Elizabeth New Jersey
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United States Furiex Research Site Garden Grove California
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United States Furiex Research Site Germantown Tennessee
United States Furiex Research Site Glendale Arizona
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United States Furiex Research Site Great Neck New York
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United States Furiex Research Site Greensboro North Carolina
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United States Furiex Research Site Houston Texas
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United States Furiex Research Site Houston Texas
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United States Furiex Research Site Port Orange Florida
United States Furiex Research Site Prince Frederick Maryland
United States Furiex Research Site Raleigh North Carolina
United States Furiex Research Site Raleigh North Carolina
United States Furiex Research Site Rapid City South Dakota
United States Furiex Research Site Rockville Maryland
United States Furiex Research Site Rome Georgia
United States Furiex Research Site Sacramento California
United States Furiex Research Site Saint Louis Missouri
United States Furiex Research Site Saint Peters Missouri
United States Furiex Research Site Saint Petersburg Florida
United States Furiex Research Site Salt Lake City Utah
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United States Furiex Research Site San Antonio Texas
United States Furiex Research Site San Antonio Texas
United States Furiex Research Site San Antonio Texas
United States Furiex Research Site San Antonio Texas
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United States Furiex Research Site Sayre Pennsylvania
United States Furiex Research Site Searcy Arkansas
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United States Furiex Research Site Shreveport Louisiana
United States Furiex Research Site South Bound Brook New Jersey
United States Furiex Research Site South Jordan Utah
United States Furiex Research Site South Miami Florida
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United States Furiex Research Site Springfield Ohio
United States Furiex Research Site Sugar Land Texas
United States Furiex Research Site Sugar Land Texas
United States Furiex Research Site Tampa Florida
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United States Furiex Research Site Tempe Arizona
United States Furiex Research Site Tempe Arizona
United States Furiex Research Site Thornton Colorado
United States Furiex Research Site Topeka Kansas
United States Furiex Research Site Troy Michigan
United States Furiex Research Site Tucson Arizona
United States Furiex Research Site Tucson Arizona
United States Furiex Research Site Tupelo Mississippi
United States Furiex Research Site Uniontown Pennsylvania
United States Furiex Research Site Vineland New Jersey
United States Furiex Research Site Virginia Beach Virginia
United States Furiex Research Site Wadsworth Ohio
United States Furiex Research Site Warwick Rhode Island
United States Furiex Research Site Washington Pennsylvania
United States Furiex Research Site Waterbury Connecticut
United States Furiex Research Site Webster Texas
United States Furiex Research Site West Jordan Utah
United States Furiex Research Site West Valley City Utah
United States Furiex Research Site Wichita Kansas
United States Furiex Research Site Wilmington North Carolina
United States Furiex Research Site Winston-Salem North Carolina
United States Furiex Research Site Winston-Salem North Carolina
United States Furiex Research Site Yukon Oklahoma

Sponsors (1)

Lead Sponsor Collaborator
Furiex Pharmaceuticals, Inc

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants Who Were Composite Responders Based on Improvements From Baseline in Daily Worst Abdominal Pain and Daily Stool Consistency Scores at Week 4 Composite responders were defined as participants who completed at least 5 out of 7 days with diary entries during the interval of interest and met both of the following criteria: 1) Average daily pain response scores over the past week improved by =30% and at least 2 points as compared with the baseline average pain score (average of daily worst abdominal pain the week prior to randomization), 2) Bristol Stool Scale (BSS) score of 3 or 4 on 66% of reported days in the past week. Abdominal pain was assessed on an 11-point scale where: 0=no pain to 10=worst pain imaginable. Stool consistency was assessed using the BSS 7-point scale where: 1=separate hard lumps, 2=sausage shaped but lumpy, 3=sausage-like with cracks on the surface, 4=sausage-like but smooth and soft, 5=soft blobs with clear cut edges, 6=fluffy pieces with ragged edges, and 7=watery with no solid pieces. Baseline (Week prior to Randomization) to Week 4
Primary Percentage of Participants Who Were Composite Responders Based on Improvements From Baseline in Daily Worst Abdominal Pain and Daily Stool Consistency Scores at Week 12 Composite responders were defined as participants who completed at least 5 out of 7 days with diary entries during the interval of interest and met both of the following criteria: 1) Average daily pain response scores over the past week improved by =30% and at least 2 points as compared with the baseline average pain score (average of daily worst abdominal pain the week prior to randomization), 2) Bristol Stool Scale (BSS) score of 3 or 4 on 66% of reported days in the past week. The participant recorded their abdominal pain in a daily diary using an 11-point scale where: 0=no pain to 10=worst pain imaginable. The participant recorded stool consistency in a daily diary using the BSS 7-point scale where: 1=separate hard lumps, 2=sausage shaped but lumpy, 3=sausage-like with cracks on the surface, 4=sausage-like but smooth and soft, 5=soft blobs with clear cut edges, 6=fluffy pieces with ragged edges, and 7=watery with no solid pieces. Baseline (Week prior to Randomization) to Week 12
Secondary Change From Baseline in the Weekly Pain Scores The participant recorded their worst daily pain score in a diary using an 11-point scale where: 0=no pain to 10=worst pain imaginable. The daily scores over the previous week were averaged. A negative change from Baseline indicates improvement. Baseline (Week Prior to Randomization) to Weeks 4, 8, and 12
Secondary Change From Baseline in Weekly BSS Scores The patient recorded stool consistency in a daily diary using the BSS 7-point scale where: 1=hard stool to 7=watery diarrhea. The daily scores over the previous week were averaged. A negative change from Baseline indicates improvement. Baseline (Week prior to Randomization) to Weeks 4, 8, and 12
Secondary Change From Baseline in the Number of Daily Bowel Movements Participants recorded the number of bowel movements in a daily diary at the same time each day. The number of daily bowel movements over the previous week were averaged. A negative change from Baseline indicates improvement. Baseline (Week prior to Randomization) to Weeks 4, 8, and 12
Secondary Percentage of Participants With Response Based on Participants Achieving Prespecified Improvement in Symptoms for at Least 50% of the Time Responders were participants that met both of the following criteria on the same week for at least 50% of time on study: 1) average of daily pain scores over the past week improved by =30% compared with baseline average in pain score, 2) =50% reduction in the number of days over the past week with a BSS score =5 compared with Baseline. Participants must also have had at least 5/7 days diary entry to be considered a responder for that week. Abdominal pain was assessed on an 11-point scale where a score of 0=no pain to 10=worst pain imaginable. Stool consistency was assessed using the BSS 7-point scale where: 1=separate hard lumps to 7=watery with no solid pieces. Response rates (percentage of participants) are based on model estimates from the logistic regression. Baseline (Week Prior to Randomization) to Weeks 1-12
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