Efficacy and Safety Trial of Elobixibat in 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

NCT01833065
000080
2012-005588-28
  • Ages > 18
  • All Genders

Study Summary

12 Week Efficacy and Safety Trial Followed by a 4 Week Withdrawal Period for Patients with Chronic Idiopathic Constipation.

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 Gastrointestinal (GI) tract or a disease orcondition that can affect 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 maneuvers (perianal pressure or digital disimpaction) or vaginalsplinting 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: 314
Study Start date:
April 01, 2013
Estimated Completion Date:
April 30, 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 12-week Treatment Period followed by a 4-week Withdrawal Period in patients with chronic idiopathic constipation. During Withdrawal Period a sub-group of patients in elobixibat 5 mg and 10 mg treatment arms respectively received placebo treatment, while rest of the patients continued with 5 mg and 10 mg treatment in respective groups. In placebo groups, patients received elobixibat 10 mg treatment during Withdrawal Period. Patients were followed-up for 2 weeks after end of the Withdrawal 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 Withdrawal Period.

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

Connect with a study center

  • Instituto Goiano de Gastroenterologia e Endoscopia Digestiva Ltda

    Goiânia, Goias
    Brazil

    Site Not Available

  • Fundacao IMEPEM - Universidade Federal de Juiz de Fora

    Juiz de Fora, Minas Gerais
    Brazil

    Site Not Available

  • Gastrocentro Carioca Centro Gast e Endosc Dig, Ltda

    Rio de Janeiro,
    Brazil

    Site Not Available

  • Hospital Israelita Albert Einstein

    São Paulo,
    Brazil

    Site Not Available

  • Medical Arts Health Research Group

    Penticton, British Columbia
    Canada

    Site Not Available

  • London Road Diagnostic Clinic and Medical Centre

    Sarnia, Ontario
    Canada

    Site Not Available

  • Dr Anil K Gupta Medicine Professional Corp.

    Toronto, Ontario
    Canada

    Site Not Available

  • Toronto Digestive Diseases Associates, Inc.

    Toronto, Ontario
    Canada

    Site Not Available

  • Pro-Recherche Polyclinique des Ponts

    Saint Romuald, Quebec
    Canada

    Site Not Available

  • Fakultní Nemocnice Ostrava

    Ostrava, Severomoravsky Kraj
    Czech Republic

    Site Not Available

  • Gastroenterologicka a interni ambulance

    Ceské Budejovice,
    Czech Republic

    Site Not Available

  • Synexus Clinical Research GmbH

    Dresden, Sachsen
    Germany

    Site Not Available

  • Synexus Clinical Research GmbH

    Görlitz, Sachsen
    Germany

    Site Not Available

  • Synexus Clinical Research GmbH

    Magdeburg, Sachsen-anhalt
    Germany

    Site Not Available

  • Pándy Kálmán Megyei Kórház

    Gyula, Bekes
    Hungary

    Site Not Available

  • Jahn Ferenc Dél-Pesti Kórház és Rendelointézet

    Budapest,
    Hungary

    Site Not Available

  • Pannónia Magánorvosi Centrum Kft.

    Budapest,
    Hungary

    Site Not Available

  • Semmelweis Egyetem

    Budapest,
    Hungary

    Site Not Available

  • Vasútegészségügyi Nonprofit Kiemelten Közhasznú Kft

    Debrecen,
    Hungary

    Site Not Available

  • Borsod Abaúj Zemplén Megyei Kórház és Egyetemi Oktató Kórház

    Miskolc,
    Hungary

    Site Not Available

  • Miskolci Semmelweis Kórház és Egyetemi Oktatókórház

    Miskolc,
    Hungary

    Site Not Available

  • Clinfan Szolgáltató Kft

    Szekszárd,
    Hungary

    Site Not Available

  • CRU Hungary Kft.

    Szikszó,
    Hungary

    Site Not Available

  • Jávorszky Ödön Kórház

    Vác,
    Hungary

    Site Not Available

  • Centro de Investigación Médico Biológica y Terapia Avanzada SC

    Guadalajara, Jalisco
    Mexico

    Site Not Available

  • Accelerium Clinical Research

    Monterrey, Nuevo Leon
    Mexico

    Site Not Available

  • Medical Care and Research

    Mérida, Yucatan
    Mexico

    Site Not Available

  • Hospital Centro Internacional de Medicina Chihuahua

    Chihuahua,
    Mexico

    Site Not Available

  • Szpital Uniwersytecki nr 2 im. dr. Jana Biziela w Bydgoszczy

    Bydgoszcz, Kujawsko-pomorskie
    Poland

    Site Not Available

  • Indywidualna Specjalistyczna Praktyka Lekarska Adam Kopon

    Torun, Kujawsko-pomorskie
    Poland

    Site Not Available

  • SPZOZ Szpital Kliniczny nr 1 im. Norberta Barlickiego Uniwersytetu Medycznego w Lodzi

    Lódz, Lodzkie
    Poland

    Site Not Available

  • Krakowskie Centrum Medyczne Sp. z o.o.

    Kraków, Malopolskie
    Poland

    Site Not Available

  • Medica Pro Familia Sp. z o.o. S.K.A.

    Warszawa, Mazowieckie
    Poland

    Site Not Available

  • Przychodnia Polskiej Fundacji Gastroenterologii Filia Nr 1 NZOZ

    Warszawa, Mazowieckie
    Poland

    Site Not Available

  • Medicor Centrum Medyczne Tadeusz Mazurek

    Rzeszów, Podkarpackie
    Poland

    Site Not Available

  • Lama Medical Care s.r.o., Gastroentero-hepatologicke centrum Thalion

    Bratislava,
    Slovakia

    Site Not Available

  • PIGEAS s.r.o.

    Martin,
    Slovakia

    Site Not Available

  • KM Management sro

    Nitra,
    Slovakia

    Site Not Available

  • Nemocica s poliklinikou Nové Mesto nad Váhom, n.o.

    Nové Mesto nad Váhom,
    Slovakia

    Site Not Available

  • Gastro I.s.r.o.

    Prešov,
    Slovakia

    Site Not Available

  • GEA s.r.o Gastroenterologicka ambulancia

    Trnava,
    Slovakia

    Site Not Available

  • JOSHA Research

    Bloemfontein, Free State
    South Africa

    Site Not Available

  • Synexus Clinical Research SA

    Pretoria, Gauteng
    South Africa

    Site Not Available

  • Dr. Zubar Fazel Vawda

    Durban, KwaZulu-Natal
    South Africa

    Site Not Available

  • Mzansi Ethical Research Centre

    Middelburg, Mpumalanga
    South Africa

    Site Not Available

  • Louis Leipoldt Medi-Clinic Medical Centre

    Bellville, Western Cape
    South Africa

    Site Not Available

  • Be Part Yoluntu Centre

    Paarl, Western Cape
    South Africa

    Site Not Available

  • Sahlgrenska University Hospital

    Gothenburg,
    Sweden

    Site Not Available

  • Karolinska University Hospital Huddinge

    Stockholm,
    Sweden

    Site Not Available

  • Uppsala Akademiska Sjukhus

    Uppsala,
    Sweden

    Site Not Available

  • Synexus Lancashire Clinical Research Centre

    Chorley, England
    United Kingdom

    Site Not Available

  • Synexus Merseyside Clinical Research Centre

    Liverpool, England
    United Kingdom

    Site Not Available

  • Synexus Thames Valley Clinical Research Centre

    Reading, England
    United Kingdom

    Site Not Available

  • Synexus Scotland Clinical Research Centre

    Glasgow, Scotland
    United Kingdom

    Site Not Available

  • Birmingham Gastroenterology Associates, PC

    Birmingham, Alabama
    United States

    Site Not Available

  • Genova Clinical Research, Inc.

    Tucson, Arizona
    United States

    Site Not Available

  • Preferred Research Partners

    Little Rock, Arkansas
    United States

    Site Not Available

  • Arkansas Gastroenterology

    North Little Rock, Arkansas
    United States

    Site Not Available

  • David Geffen School of Medicine at University of California, Los Angeles

    Los Angeles, California
    United States

    Site Not Available

  • West Gastroenterology Associates

    Los Angeles, California
    United States

    Site Not Available

  • Sacramento Research Medical Group

    Sacramento, California
    United States

    Site Not Available

  • Precision Research Institute, LLC

    San Diego, California
    United States

    Site Not Available

  • Gastroenterology Associates of Fairfield County

    Bridgeport, Connecticut
    United States

    Site Not Available

  • Zasa Clinical Research

    Boynton Beach, Florida
    United States

    Site Not Available

  • Meridien Research

    Bradenton, Florida
    United States

    Site Not Available

  • Sanitas Research

    Coral Gables, Florida
    United States

    Site Not Available

  • Lake Internal Medicine Associates

    Eustis, Florida
    United States

    Site Not Available

  • Health Care Family Rehab Corp.

    Hialeah, Florida
    United States

    Site Not Available

  • Southeast Clinical Research, LLC

    Jacksonville, Florida
    United States

    Site Not Available

  • Health Awareness, Inc.

    Jupiter, Florida
    United States

    Site Not Available

  • Mount Vernon Clinical Research

    Atlanta, Georgia
    United States

    Site Not Available

  • Southeast Regional Research Group

    Columbus, Georgia
    United States

    Site Not Available

  • Premier Healthcare Research, LLC

    Evanston, Illinois
    United States

    Site Not Available

  • Rockford Gastroenterology Associates, Ltd.

    Rockford, Illinois
    United States

    Site Not Available

  • Heartland Research Associates, LLC

    Augusta, Kansas
    United States

    Site Not Available

  • Heartland Research Associates, LLC

    Wichita, Kansas
    United States

    Site Not Available

  • Professional Research Network of Kansas, LLC

    Witchita, Kansas
    United States

    Site Not Available

  • Louisiana Research Center, LLC

    Shreveport, Louisiana
    United States

    Site Not Available

  • Beacon Clinical Research, LLC

    Brockton, Massachusetts
    United States

    Site Not Available

  • Mayo Clinic

    Rochester, Minnesota
    United States

    Site Not Available

  • Quality Clinical Research, Inc.

    Omaha, Nebraska
    United States

    Site Not Available

  • Mount Vernon Clinical Research

    Brooklyn, New York
    United States

    Site Not Available

  • Long Island Gastrointestinal Research Group

    Great Neck, New York
    United States

    Site Not Available

  • Carolina Digestive Health Associates, PA

    Charlotte, North Carolina
    United States

    Site Not Available

  • Carolina Digestive Health Associates, PA

    Concord, North Carolina
    United States

    Site Not Available

  • PharmQuest, LLC

    Greensboro, North Carolina
    United States

    Site Not Available

  • Peters Medical Research, LLC

    High Point, North Carolina
    United States

    Site Not Available

  • Wake Research Associates, LLC

    Raleigh, North Carolina
    United States

    Site Not Available

  • Hometown Urgent Care and Occupational Health

    Columbus, Ohio
    United States

    Site Not Available

  • Hometown Urgent Care and Occupational Health

    Dayton, Ohio
    United States

    Site Not Available

  • Family Practice Center of Wadsworth

    Wadsworth, Ohio
    United States

    Site Not Available

  • Clinical Research Associates, LLC

    Oklahoma City, Oklahoma
    United States

    Site Not Available

  • Sunstone Medical Research, LLC

    Medford, Oregon
    United States

    Site Not Available

  • Family Medical Associates

    Levittown, Pennsylvania
    United States

    Site Not Available

  • Anderson Gastroenterology Associates

    Anderson, South Carolina
    United States

    Site Not Available

  • Palmetto Clinical Research

    Summerville, South Carolina
    United States

    Site Not Available

  • Associates in Gastroenterology, LLC

    Hermitage, Tennessee
    United States

    Site Not Available

  • HCCA Clinical Research Solutions

    Jackson, Tennessee
    United States

    Site Not Available

  • New Phase Research and Development, LLC

    Knoxville, Tennessee
    United States

    Site Not Available

  • Research Across America

    Katy, Texas
    United States

    Site Not Available

  • Gastroenterology Associates of Tidewater

    Chesapeake, Virginia
    United States

    Site Not Available

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