26 Week Efficacy and Safety Trial for Patients With Chronic Idiopathic Constipation

Last updated: September 22, 2015
Sponsor: Ferring Pharmaceuticals
Overall Status: Terminated

Phase

3

Condition

Irritable Bowel Syndrome (Ibs)

Constipation

Treatment

N/A

Clinical Study ID

NCT01827592
000079
2012-005587-94
  • Ages > 18
  • All Genders

Study Summary

Efficacy and Safety Trial of elobixibat in Patients with Chronic Idiopathic Constipation treated for 26 Weeks.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Body mass index (BMI) ≥18.5 but <35.0 kg/m^2

  • Male or female ≥18 years of age

  • Reports <3 spontaneous Bowel movements (BM) per week and reports one or more of thefollowing symptoms for the last 3 months with symptom onset at least 6 months beforethe Screening Visit or before starting chronic therapy with any laxative:

  1. Straining during at least 25% of defecations

  2. Lumpy or hard stools during at least 25% of defecations

  3. Sensation of incomplete evacuation during at least 25% of defecations

  • Is ambulatory and community dwelling

  • An initial colonoscopy is required if recommended by national guidelines

Exclusion

Exclusion Criteria:

  • Reports loose (mushy) or watery stools in the absence of any laxative intake in theform of a tablet, a suppository or an enema, or prohibited medicine for >25% of BMs

  • The patient reports a BSFS of 6 or 7 during the Pretreatment Period

  • Has irritable bowel syndrome (IBS) with pain/discomfort as predominant symptoms

  • Has a structural abnormality of the GI tract or a disease or condition that can affectGastrointestinal (GI) motility

  • Has a history of diverticulitis, chronic pancreatitis, active peptic ulcer disease (PUD) not adequately treated, ischaemic colitis, inflammatory bowel disease, laxativeabuse, faecal impaction that required hospitalization or emergency treatment,pseudo-obstruction, megacolon, megarectum, bowel obstruction, descending perineumsyndrome, ovarian cysts, endometriosis, solitary rectal ulcer syndrome, systemicsclerosis, pre-malignant colonic disease (e.g., familial adenomatous polyposis orhereditary non-polyposis colorectal cancer) or other forms of familial colorectalcancer.

  • Has unexplained and clinically significant GI alarm signals (e.g., lower GI bleedingor heme-positive stool in the absence of known internal or external haemorrhoids,iron-deficiency anaemia, unexplained weight loss) or systemic signs of infection orcolitis

  • Has a potential central nervous system (CNS) cause of constipation (e.g., Parkinson'sdisease, spinal cord injury, multiple sclerosis)

  • Has intestinal/rectal prolapse or other known pelvic floor dysfunction

  • Commonly uses digital manoeuvres (perianal pressure or digital disimpaction) orvaginal splinting to facilitate the passage of a bowel movement

  • Has a history of diabetic neuropathy

  • Has a history of bariatric surgery for treatment of obesity; surgery to remove asegment of the GI tract; or surgery of the abdomen, pelvic or retroperitoneal areaduring the 6 months prior to Screening; or appendectomy or cholecystectomy 3 monthsprior to screening; or other major surgery 1 month prior to Screening

  • Has a history of cancer with last date of proven disease activity/presence ofmalignancy within 5 years, except for adequately treated basal cell carcinoma of theskin, cervical dysplasia, or carcinoma in situ of the skin or the cervix

  • Known human immunodeficiency virus (HIV) or Hepatitis B/C (HBV/HCV) infection

  • Has a history of hospitalization for any psychiatric disorder, or any suicide attemptin the 2 years prior to Screening

  • Is actively abusing alcohol or drugs or has a history of alcohol or drug abuse duringthe 6 months prior to Screening

  • Is being treated for hypothyroidism, but the dose of medication has not been stablefor at least 3 months at the time of Screening

  • Is a pregnant, breast-feeding, or lactating woman

Study Design

Total Participants: 376
Study Start date:
April 01, 2013
Estimated Completion Date:
May 31, 2014

Study Description

The present trial was designed to determine the efficacy and safety of elobixibat treatment (at both doses of 5 mg and 10 mg/day) compared to placebo treatment for 26-week Treatment Period in patients with chronic idiopathic constipation. Patients were followed-up for 2 weeks after end of the Treatment Period.

The assessment of primary and key secondary end points was done for patients who completed the first 12 weeks of Treatment Period. Incidence of Adverse Events (AEs) were reported till 2 weeks after end of the treatment.

The trial was early terminated due to a distribution issue with the trial medication.

Connect with a study center

  • Cliniques Universitaires Saint Luc

    Brussels,
    Belgium

    Site Not Available

  • Huisartspraktijk Jaak Mortelmans

    Ham,
    Belgium

    Site Not Available

  • Universitair Ziekenhuis Leuven

    Leuven,
    Belgium

    Site Not Available

  • Hospital de Clinicas de Porto Alegre

    Porto Alegre, Rio Grande do Sul
    Brazil

    Site Not Available

  • Faculdade de Medicina do ABC

    Sant André, São Paulo
    Brazil

    Site Not Available

  • Escola Paulista de Medicina, Universidade Federal de São Paulo

    São Paulo,
    Brazil

    Site Not Available

  • John Buhler Research Center

    Winnipeg, Manitoba
    Canada

    Site Not Available

  • Maritime Medical Research Center

    Bathurst, New Brunswick
    Canada

    Site Not Available

  • Prime Health Clinical Research Organization

    Toronto, Ontario
    Canada

    Site Not Available

  • Alpha Clinical Research LLC

    Québec, Quebec
    Canada

    Site Not Available

  • Rhodin Recherche Clinique

    DrummondvilleQC,
    Canada

    Site Not Available

  • Derma Plus s.r.o.

    Ceské Budejovice,
    Czech Republic

    Site Not Available

  • Gastroenterologie, s. r. o.

    Hradec Králové,
    Czech Republic

    Site Not Available

  • Nemocnice Valasske Mezirici a.s., Gastroenterologicka ambulance

    Valasske Mezirici,
    Czech Republic

    Site Not Available

  • Klinikum der Universität München-Großhadern

    München, Bavaria
    Germany

    Site Not Available

  • Synexus Clinical Research GmbH

    Frankfurt am Main, Hessen
    Germany

    Site Not Available

  • Elbe Klinikum Stade - Buxtehude GmbH

    Stade, Niedersachsen
    Germany

    Site Not Available

  • Synexus Clinical Research GmbH

    Bochum, Nordrhein-westfalen
    Germany

    Site Not Available

  • Synexus Clinical Research GmbH

    Leipzig, Sachsen
    Germany

    Site Not Available

  • Emovis GmbH

    Berlin,
    Germany

    Site Not Available

  • Synexus Clinical Research GmbH

    Berlin,
    Germany

    Site Not Available

  • Universitätsklinik Charité, Campus Mitte

    Berlin,
    Germany

    Site Not Available

  • Israelitisches Krankenhaus Hamburg

    Hamburg,
    Germany

    Site Not Available

  • Soroka University Medical Center

    Beer-Sheva,
    Israel

    Site Not Available

  • Bnai Zion Medical Center

    Haifa,
    Israel

    Site Not Available

  • Hadassah Medical Organization, Ein Kerem

    Jerusalem,
    Israel

    Site Not Available

  • Kaplan Medical Center

    Rehovot,
    Israel

    Site Not Available

  • Sheba Medical Center

    Tel Hashomer,
    Israel

    Site Not Available

  • Assaf Harofeh Medical Centre

    Zerifin,
    Israel

    Site Not Available

  • SPZOZ Uniwersytecki Szpital Kliniczny nr 5 im. Gen. Dyw. B. Szareckiego, Uniwersytetu Medycznego

    Lódz, Lodzkie
    Poland

    Site Not Available

  • Szpital Wojewódzki w Opolu

    Opole, Opolskie
    Poland

    Site Not Available

  • Centrum Medyczne sw. Lukasza Sp. z o.o.

    Czestochowa, Slaskie
    Poland

    Site Not Available

  • Neuro-Care NZOZ

    Katowice, Slaskie
    Poland

    Site Not Available

  • Pomorski Uniwersytet Medyczny

    Szczecin, Zachodniopomorskie
    Poland

    Site Not Available

  • Global Clinical Trials

    Port Elizabeth, Eastern Cape
    South Africa

    Site Not Available

  • Boanerges Clinical Research

    Bloemfontein, Free State
    South Africa

    Site Not Available

  • Synexus Clinical Research SA

    Pretoria, Gauteng
    South Africa

    Site Not Available

  • Parklands Medical Centre

    Durban, KwaZulu-Natal
    South Africa

    Site Not Available

  • Boland Ethical Research Group

    Worcester, Western Cape
    South Africa

    Site Not Available

  • The Memory Centre

    Johannesburg,
    South Africa

    Site Not Available

  • Langeberg Clinical Trials

    Kraaifontein,
    South Africa

    Site Not Available

  • Newtown Clinical Research Centre

    Newtown,
    South Africa

    Site Not Available

  • Synexus Midlands Clinical Research Centre

    Birmingham, England
    United Kingdom

    Site Not Available

  • County Durham and Darlington NHS Foundation Trust

    Durham, England
    United Kingdom

    Site Not Available

  • Synexus Manchester Clinical Research Centre

    Manchester, England
    United Kingdom

    Site Not Available

  • Tayside University Hospitals NHS Trust, Ninewells Hospital and Medical School

    Dundee, Scotland
    United Kingdom

    Site Not Available

  • Synexus Wales Clinical Research Centre

    Cardiff, Wales
    United Kingdom

    Site Not Available

  • Nottingham University Hospitals NHS Trust

    Nottingham,
    United Kingdom

    Site Not Available

  • Alabama Clinical Therapeutics

    Birmingham, Alabama
    United States

    Site Not Available

  • G and L Research, LLC

    Foley, Alabama
    United States

    Site Not Available

  • Adobe Gastroenterology Research, LLC

    Tucson, Arizona
    United States

    Site Not Available

  • Skyline Research LLC

    Cerritos, California
    United States

    Site Not Available

  • GW Research, Inc.

    Chula Vista, California
    United States

    Site Not Available

  • Paradigm Clinical, Inc.

    Garden Grove, California
    United States

    Site Not Available

  • Providence Clinical Research

    North Hollywood, California
    United States

    Site Not Available

  • Stamford Therapeutics Consortium

    Stamford, Connecticut
    United States

    Site Not Available

  • Pulmonary Associates of Brandon

    Brandon, Florida
    United States

    Site Not Available

  • In Vivo Clinical Research, Inc.

    Hialeah, Florida
    United States

    Site Not Available

  • Medsearch Professional Group, Inc.

    Hialeah, Florida
    United States

    Site Not Available

  • The Community Research of South Florida

    Hialeah, Florida
    United States

    Site Not Available

  • Center for Gastrointestinal Disorders

    Hollywood, Florida
    United States

    Site Not Available

  • Nature Coast Clinical Research, LLC

    Inverness, Florida
    United States

    Site Not Available

  • Gastroenterology and Hepatology Associates

    Jacksonville, Florida
    United States

    Site Not Available

  • Jupiter Research Inc.

    Jupiter, Florida
    United States

    Site Not Available

  • Center for Advanced Gastroenterology

    Maitland, Florida
    United States

    Site Not Available

  • Advanced Pharma CR, LLC

    Miami, Florida
    United States

    Site Not Available

  • Research Institute of South Florida

    Miami, Florida
    United States

    Site Not Available

  • Gastroenterology Group of Naples

    Naples, Florida
    United States

    Site Not Available

  • Palm Beach Research Center

    West Palm Beach, Florida
    United States

    Site Not Available

  • Georgia Clinical Research

    Snellville, Georgia
    United States

    Site Not Available

  • Elite Clinical Trials, Inc.

    Blackfoot, Idaho
    United States

    Site Not Available

  • MediSphere Medical Research Center, LLC

    Evansville, Indiana
    United States

    Site Not Available

  • MidAtlantic Medical Research Centers, Philip J. Bean Medical Center

    Hollywood, Maryland
    United States

    Site Not Available

  • Boston Clinical Trials

    Boston, Massachusetts
    United States

    Site Not Available

  • University of Michigan Health System

    Ann Arbor, Michigan
    United States

    Site Not Available

  • Midwest Gastroenterology Partners

    Lee's Summit, Missouri
    United States

    Site Not Available

  • Advanced Biomedical Research of America

    Las Vegas, Nevada
    United States

    Site Not Available

  • ActivMed Practices and Research, Inc.

    Newington, New Hampshire
    United States

    Site Not Available

  • HOSC, Inc.

    Brooklyn, New York
    United States

    Site Not Available

  • North American Partners in Pain Management

    Valley Stream, New York
    United States

    Site Not Available

  • Carolina Digestive Health Associates, PA

    Davidson, North Carolina
    United States

    Site Not Available

  • Cumberland Research Associates, LLC

    Fayetteville, North Carolina
    United States

    Site Not Available

  • Gastroenterology Research Consultants of Greater Cincinnati

    Cincinnati, Ohio
    United States

    Site Not Available

  • Hometown Urgent Care and Occupational Health

    Groveport, Ohio
    United States

    Site Not Available

  • Oklahoma Foundation for Digestive Research

    Oklahoma City, Oklahoma
    United States

    Site Not Available

  • Clinical Trials Research Services, LLC

    Pittsburgh, Pennsylvania
    United States

    Site Not Available

  • Mainline Gastroenterology Associates

    Souderton, Pennsylvania
    United States

    Site Not Available

  • ClinSearch

    Chattanooga, Tennessee
    United States

    Site Not Available

  • Memphis Gastroenterology Group, PC

    Germantown, Tennessee
    United States

    Site Not Available

  • KRK Medical Research

    Dallas, Texas
    United States

    Site Not Available

  • Research Across America

    Dallas, Texas
    United States

    Site Not Available

  • Pioneer Research Solutions, Inc.

    Houston, Texas
    United States

    Site Not Available

  • Pioneer Research Solutions, Inc.

    Sugar Land, Texas
    United States

    Site Not Available

  • Northwest Gastroenterology Associates

    Bellevue, Washington
    United States

    Site Not Available

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