Current partner codePEPTIDESDE
NCT01880424·Phase 3·INTERVENTIONAL

A Phase 3, International, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Efficacy and Safety Trial of Linaclotide Administered Orally for 12 Weeks to Patients With Irritable Bowel Syndrome With Constipation (IBS-C)

Status

Completed

Phase

Phase 3

Enrollment

1,722

Locations

82

Results

Posted

Publications

1

Study summary

What the protocol is testing.

This clinical trial is an international, multicenter, randomized, double-blind, placebo-controlled, parallel-group trial comparing one dose of linaclotide to placebo. Approximately 800 patients with a diagnosis of IBS-C (modified Rome III criteria) will be randomized at up to 60 trial centers in China, Australia, and New Zealand. The trial will consist of up to 21 days of screening, 14 to 21 days of pre-treatment, 12 weeks of double-blind treatment, and 2 weeks of follow-up. At the end of the Pre-treatment Period, patients meeting the entry criteria for this trial will be randomized to one of two double-blind treatment groups: 290 ug linaclotide, or placebo (1:1).

Interventions

Treatment arms and agents.

DRUG

Placebo

matching Placebo Capsules, Oral, once daily

DRUG

Linaclotide

Linaclotide 290 ug Capsules, Oral, once daily

Timeline

From registration to results.

  1. First posted

    Jun 19, 2013

  2. Study start

    Jul 2013

  3. Primary completion

    May 2015

  4. Study completion

    May 2015

  5. Results posted

    Sep 27, 2016

  6. Registry updated

    Sep 27, 2016

Outcomes

What the study measures.

Primary outcomes

12-week Abdominal Pain/Abdominal Discomfort Weekly Responder

Time frame · Baseline and Weeks 1-12 during the Treatment Period

A 12-week Abdominal Pain/Abdominal Discomfort Responder is a patient who meets the Abdominal Pain/Abdominal Discomfort Weekly Responder criteria (i.e., an improvement of ≥30% from baseline in either the mean abdominal pain score or mean abdominal discomfort score for that week, with neither score worsening from baseline for that week) for at least 6 out of the 12 weeks of the Treatment Period. Abdominal pain at its worst (in the last 24 hours) was assessed daily by patients on an 11-point numerical rating scale (NRS) where 0 represents no abdominal pain and 10 represents very severe abdominal pain. Abdominal discomfort (in the last 24 hours) was assessed daily by patients on an 11-point NRS where 0 represents no abdominal discomfort and 10 represents very severe abdominal discomfort.

12-week Irritable Bowel Syndrome (IBS) Degree of Relief Responder

Time frame · Baseline and Weeks 1-12 during the Treatment Period

A 12-week IBS Degree of Relief Responder is a patient who meets the IBS Degree of Relief Weekly Responder criteria (i.e., response to the degree of relief of IBS symptoms question for that week was "Considerably relieved" or "Completely relieved") for at least 6 out of the 12 weeks of the Treatment Period. Degree of relief of IBS symptoms (in the last 7 days) was assessed weekly by patients on a 7-point balanced ordinal scale where 1 = Completely relieved, 4 = Unchanged, and 7 = As bad as I can imagine.

Secondary outcomes

Change From Baseline in 12-week Complete Spontaneous Bowel Movement Frequency Rate

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week CSBM frequency (i.e., average weekly CSBM frequency over the 12 weeks of the Treatment Period). A spontaneous bowel movement (SBM) is defined as a bowel movement without laxative use in the preceding 24 hours. A CSBM is defined as an SBM that is associated with a sense of complete evacuation.

Change From Baseline in 12-week Spontaneous Bowel Movement Frequency Rate

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week SBM frequency (i.e., average weekly SBM frequency over the 12 weeks of the Treatment Period). SBM is defined as a bowel movement without laxative use in the preceding 24 hours.

Change From Baseline in 12-week Stool Consistency

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week stool consistency (i.e., the average of the non-missing Bristol Stool Form Scale \[BSFS\] score from the SBMs occurring during the 12-week Treatment Period). Consistency of each bowel movement was assessed daily by patients using the 7-point BSFS (1=Separate hard lumps like nuts \[difficult to pass\] to 7=Watery, no solid pieces \[entirely liquid\]).

Change From Baseline in 12-week Severity of Straining

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week severity of straining (i.e., the average of the non-missing straining scores from the SBMs occurring during the 12-week Treatment Period). Severity of straining was assessed daily by patients on a 5-point ordinal scale (1=Not at all to 5=An extreme amount).

Change From Baseline in 12-week Abdominal Bloating

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week abdominal bloating (i.e., the average of the non-missing daily abdominal bloating scores reported during the 12-week Treatment Period). Abdominal bloating (in the last 24 hours) was assessed daily by patients on an 11-point NRS where 0 represents no abdominal bloating and 10 represents very severe abdominal bloating.

Change From Baseline in 12-week Abdominal Pain

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week abdominal pain (i.e., the average of the non-missing daily abdominal pain scores reported during the 12-week Treatment Period). Abdominal pain at its worst (in the last 24 hours) was assessed daily by patients on an 11-point NRS where 0 represents no abdominal pain and 10 represents very severe abdominal pain.

Change From Baseline in 12-week Abdominal Discomfort

Time frame · Baseline and 12-week Treatment Period

The change from baseline in 12-week abdominal discomfort (i.e., the average of the non-missing daily abdominal discomfort scores reported during the 12-week Treatment Period). Abdominal discomfort (in the last 24 hours) was assessed daily by patients on an 11-point NRS where 0 represents no abdominal discomfort and 10 represents very severe abdominal discomfort.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: 1. Patient has signed an Informed Consent Form(ICF). 2. Patient Must not be pregnant or breastfeeding and agree to use birth control 3. Patient meets the colonoscopy requirements defined by the American Gastroenterological Association guidelines and no clinically-significant laboratory or physical examination findings; 4. Patient meets protocol-defined criteria for Irritable Bowel Syndrome with Constipation(IBS-C), including stool frequency, straining, stool consistency, abdominal pain, and abdominal discomfort criteria 5. Patient meets protocol-defined eDiary completion Compliance and agrees to refrain from making any new, major life-style changes that may affect IBS-C symptoms Exclusion Criteria: 1. Recent history of mushy or watery stools 2. Various medical conditions, medical histories, or family medical histories that would not make the patient a good candidate for the study 3. Patient currently has both unexplained and clinically significant alarm symptoms or systemic signs of infection or colitis. 4. Surgery to the gastrointestinal tract 5. Usage of prohibited medications

Study locations

82 registered sites.

Australia · Canada · China · New Zealand · United States. Showing up to 24 locations stored in the fast local snapshot.

Research Site

Huntsville, Alabama, United States

Research Site

North Little Rock, Arkansas, United States

Research Site

Phoenix, Arkansas, United States

Research Site

Artesia, California, United States

Research Site

Chula Vista, California, United States

Research Site

Encino, California, United States

Research Site

North Hollywood, California, United States

Research Site

Orange, California, United States

Research Site

Riverside, California, United States

Research Site

San Diego, California, United States

Research Site

Boynton Beach, Florida, United States

Research Site

Brandon, Florida, United States

Research Site

Brooksville, Florida, United States

Research Site

Doral, Florida, United States

Research Site

Gainesville, Florida, United States

Research Site

Hialeah, Florida, United States

Research Site

Kissimmee, Florida, United States

Research Site

Lauderdale Lakes, Florida, United States

Research Site

Miami, Florida, United States

Research Site

Miami Lakes, Florida, United States

Research Site

Addison, Illinois, United States

Research Site

Evansville, Indiana, United States

Research Site

Crowley, Louisiana, United States

Research Site

Monroe, Louisiana, United States

Related trials

More studies on Linaclotide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.