Study of Elobixibat (A3309) in Patients With Chronic Idiopathic Constipation (ACCESS)

February 1, 2017 updated by: Albireo

A Phase IIb, Double-blind, Randomised, Placebo-controlled, Multi-centre, Dose-finding Efficacy and Safety Study of a Range of Doses of Elobixibat in Patients With Chronic Idiopathic Constipation

The purpose of this trial is to determine the efficacy and safety of A3309 administered to patients with chronic idiopathic constipation.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
190

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Alabama
      • Huntsville, Alabama, United States, 35801
        • Albireo Investigative Site
    • Arizona
      • Chandler, Arizona, United States, 85224
        • Albireo Investigative Site
      • Phoenix, Arizona, United States, 85020
        • Albireo Investigative Site
    • California
      • Anaheim, California, United States, 92801
        • Albireo Investigative Site
      • Encinitas, California, United States, 92024
        • Albireo Investigative Site
      • San Diego, California, United States, 92108
        • Albireo Investigative Site
    • Colorado
      • Colorado Springs, Colorado, United States, 80904
        • Albireo Investigative Site
    • Florida
      • Boynton Beach, Florida, United States, 33426
        • Albireo Investigative Site
      • Inverness, Florida, United States, 34452
        • Albireo Investigative Site
    • Illinois
      • Peoria, Illinois, United States, 61602
        • Albireo Investigative Site
    • Iowa
      • Clive, Iowa, United States, 50325
        • Albireo Investigative Site
      • Davenport, Iowa, United States, 52807
        • Albireo Investigative Site
    • Kansas
      • Mission, Kansas, United States, 66202
        • Albireo Investigative Site
      • Overland Park, Kansas, United States, 66215
        • Albireo Investigative Site
    • Louisiana
      • Monroe, Louisiana, United States, 71201
        • Albireo Investigative Site
      • Shreveport, Louisiana, United States, 71103
        • Albireo Investigative Site
    • Maryland
      • Annapolis, Maryland, United States, 21401
        • Albireo Investigative Site
      • Baltimore, Maryland, United States, 21215
        • Albireo Investigative Site
      • Hollywood, Maryland, United States, 20636
        • Albireo Investigative Site
    • Michigan
      • Chesterfield, Michigan, United States, 48047
        • Albireo Investigative Site
    • Nevada
      • Henderson, Nevada, United States, 89104
        • Albireo Investigative Site
    • New Jersey
      • Marlton, New Jersey, United States, 08053
        • Albireo Investigative Site
    • New Mexico
      • Albuquerque, New Mexico, United States, 87108
        • Albireo Investigative Site
    • New York
      • Great Neck, New York, United States, 11021
        • Albireo Investigative Site
    • North Carolina
      • Charlotte, North Carolina, United States, 28211
        • Albireo Investigative Site
      • Greensboro, North Carolina, United States, 27408
        • Albireo Investigative Site
      • Harrisburg, North Carolina, United States, 28075
        • Albireo Investigative Site
      • Statesville, North Carolina, United States, 28625
        • Albireo Investigative Site
      • Winston-Salem, North Carolina, United States, 27103
        • Albireo Investigative Site
    • Ohio
      • Cincinnati, Ohio, United States, 45224
        • Albireo Investigative Site
      • Cincinnati, Ohio, United States, 45242
        • Albireo Investigative Site
      • Dayton, Ohio, United States, 45440
        • Albireo Investigative Site
    • Oklahoma
      • Oklahoma City, Oklahoma, United States, 73116
        • Albireo Investigative Site
    • Pennsylvania
      • Levittown, Pennsylvania, United States, 19056
        • Albireo Investigative Site
    • South Carolina
      • Anderson, South Carolina, United States, 29621
        • Albireo Investigative Site
    • Tennessee
      • Chattanooga, Tennessee, United States, 37411
        • Albireo Investigative Site
      • Kingsport, Tennessee, United States, 37660
        • Albireo Investigative Site
    • Texas
      • El Paso, Texas, United States, 79905
        • Albireo Investigative Site
      • Longview, Texas, United States, 75605
        • Albireo Investigative Site
      • San Antonio, Texas, United States, 78229
        • Albireo Investigative Site
    • Utah
      • Ogden, Utah, United States, 84405
        • Albireo Investigative Site
      • Salt Lake City, Utah, United States, 84107
        • Albireo Investigative Site
    • Virginia
      • Lynchburg, Virginia, United States, 24502
        • Albireo Investigative Site
    • Wisconsin
      • La Crosse, Wisconsin, United States, 54601
        • Albireo Investigative Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

20 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patient meets protocol specified criteria for constipation
  • Patient has successfully completed study requirements with no clinically relevant findings for physical exam, ECG, laboratory tests and colonoscopy as applicable

Exclusion Criteria:

  • Medical history or medical condition that would not make the patient a good candidate for the study or limit the patient´s ability to complete the study
  • Patient reports loose stools
  • Patient has IBS with pain/discomfort as predominant symptom
  • Patient needs medications prohibited as specified in the protocol

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: A3309 low dose
Administered once daily for the duration of the study
Drug: A3309
A3309 in three different dosage levels or placebo once daily for the duration of the study
Experimental: A3309 intermediate dose
Administered once daily for the duration of the study.
Drug: A3309
A3309 in three different dosage levels or placebo once daily for the duration of the study
Experimental: A3309 high dose
Administered once daily for the duration of the study
Drug: A3309
A3309 in three different dosage levels or placebo once daily for the duration of the study
Placebo Comparator: Placebo
Administered once daily for the duration of the study
Drug: A3309
A3309 in three different dosage levels or placebo once daily for the duration of the study

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Change From Baseline in Frequency of Spontaneous Bowel Movements
Time Frame: Baseline, weekly, up to 8 weeks
Primary ep W 1
Baseline, weekly, up to 8 weeks

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Responder Analyses for Complete Spontaneous Bowel Movements (CSBMs)
Time Frame: Baseline, weekly and up to 8 weeks

A CSBM responder is defined as per FDA draft guidance for IBS-C:

An increase of one or more of CSBMs per week over baseline for at least 4 out of the 8 weeks of treatment
Baseline, weekly and up to 8 weeks
Time to First Bowel Movement
Time Frame: First week
First week
Stool Consistency Change From Baseline
Time Frame: Baseline, weekly and up to 8 weeks
Bristol Stool Form Scale. Min value:1. Max value: 7. Higher value indicates more liquid shape than normal, lower indicates constipated state.
Baseline, weekly and up to 8 weeks
LDL/HDL Ratio
Time Frame: Baseline and 8 weeks of treatment
Ratio of plasma LDL cholesterol and HDL cholesterol Difference from baseline, placebo-adjusted
Baseline and 8 weeks of treatment
Straining Change From Baseline
Time Frame: Baseline and during 8 weeks of treatment
Daily assessment of straining. Min value: 1. Max value: 5. Higher value indicates more straining.
Baseline and during 8 weeks of treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Albireo

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Chair: Hans Graffner, MD, Albireo

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
November 1, 2009

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
October 1, 2010

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
October 1, 2010

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
November 2, 2009

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 2, 2009

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
November 3, 2009

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
March 22, 2017

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 1, 2017

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
February 1, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • A3309-002

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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