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Phase 2a Study of IW-9179 to Treat Functional Dyspepsia

Primary Purpose

Dyspepsia, Functional Gastrointestinal Disorders

Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
IW-9179
Placebo
Sponsored by
Ironwood Pharmaceuticals, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dyspepsia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient meets ROME III criteria for functional dyspepsia (FD)
  • Patient has a normal esophagogastroduodenoscopy (EGD) either during the Screening Period or within 2 years of the Screening Visit
  • Patients who EITHER:

    1. Have not used a proton pump inhibitor (PPI) within 4 weeks of the Screening Visit, OR
    2. Have used a PPI at a stable dose for at least 4 weeks prior to the Screening Visit;
  • Patient meets symptom severity criteria in the Pretreatment Period
  • Patient is fluent and literate in Dutch, French, or English

Exclusion Criteria:

  • Patient meets criteria for gastroesophageal reflux disease (GERD, stable regimen of PPIs acceptable), constipation, diarrhea, lower abdominal pain, or gastroparesis
  • Patient has a history of inflammatory bowel disease, chronic pancreatitis, small intestinal bacterial overgrowth, celiac disease, lactose intolerance, polycystic kidney disease, interstitial cystitis, or scleroderma
  • Any significant neurological disease or a history of cancer (resected basal cell or squamous cell carcinoma of the skin is acceptable; complete remission of other cancers for 5 years or longer is also acceptable)
  • History of active alcoholism or drug addiction within 12 months prior to the Screening Visit
  • Hospitalized for a psychiatric condition or has made a suicide attempt during the two years before the Screening Visit
  • Any organic or structural disease that can cause abdominal pain or discomfort

Sites / Locations

  • AZ Sint-Lucas Brugge
  • Antwerp University Hospital
  • Z.O.L. - Campus St. Jan
  • Universitair Ziekenhuis Gent
  • UZ Leuven
  • CHU Ambroise Pare
  • H. Hartziekenhuis Roselare-Menen vzw
  • FlevoResearch
  • PreCare Trial and Recruitment
  • Andromed Breda
  • Andromed Eindhoven
  • Andromed Noord
  • Andromed Leiden
  • Maastricht University Med Ctr
  • Andromed Rotterdam

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

IW-9179

Placebo

Arm Description

Oral IW-9179 taken daily for two weeks

Oral placebo taken daily for two weeks

Outcomes

Primary Outcome Measures

Rate of treatment-emergent adverse events
Change from baseline 12-lead electrocardiogram (ECG) at day 14 of treatment
Change from baseline clinical laboratory evaluations at the last day of treatment (day 14)
Change from baseline vital signs at the day 14 visit and at the end of the study (7 days after the last dose)

Secondary Outcome Measures

Post-meal Symptom Severity (PMSS) Assessment
Assessments completed at 15 min prior to dose, just prior to dose, and every 15 minutes after the first dose through 240 minutes (4 hours after first dose)
Daily Patient Symptom Severity (PSS) Assessment
Assessments recorded on a daily basis
Weekly Symptom Relief (SR) Assessments
Assessments recorded on a weekly basis weekly
Nepean Dyspepsia Index

Full Information

First Posted
October 11, 2012
Last Updated
March 18, 2014
Sponsor
Ironwood Pharmaceuticals, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01712412
Brief Title
Phase 2a Study of IW-9179 to Treat Functional Dyspepsia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Terminated
Why Stopped
Slow enrollment
Study Start Date
October 2012 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ironwood Pharmaceuticals, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objectives of this study are to determine the safety and efficacy of IW-9179 administered to patients with functional dyspepsia (FD).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyspepsia, Functional Gastrointestinal Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
IW-9179
Arm Type
Experimental
Arm Description
Oral IW-9179 taken daily for two weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Oral placebo taken daily for two weeks
Intervention Type
Drug
Intervention Name(s)
IW-9179
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Rate of treatment-emergent adverse events
Time Frame
Reported at any time after the first dose, including the 14 days of treatment and 7 days of follow up
Title
Change from baseline 12-lead electrocardiogram (ECG) at day 14 of treatment
Time Frame
Baseline values taken just prior to first dose (day 1) compared with values taken on the last day of treatment (day 14)
Title
Change from baseline clinical laboratory evaluations at the last day of treatment (day 14)
Time Frame
Baseline values taken just prior to first dose (day 1) compared with values taken on the last day of treatment (day 14)
Title
Change from baseline vital signs at the day 14 visit and at the end of the study (7 days after the last dose)
Time Frame
Baseline values taken prior to first dose (day 1) compared with values taken at the day 14 visit (14 days after first dose) and at the end of the study (21 days after the first dose)
Secondary Outcome Measure Information:
Title
Post-meal Symptom Severity (PMSS) Assessment
Description
Assessments completed at 15 min prior to dose, just prior to dose, and every 15 minutes after the first dose through 240 minutes (4 hours after first dose)
Time Frame
Completed at day 1 and day 14 of the Treatment Period
Title
Daily Patient Symptom Severity (PSS) Assessment
Description
Assessments recorded on a daily basis
Time Frame
Average of daily assessments for the 2 weeks just prior to the first dose compared to: 1) the average of the 2 week treatment period, 2) the average of the first week of treatment and 3) the average of the second week of treatment
Title
Weekly Symptom Relief (SR) Assessments
Description
Assessments recorded on a weekly basis weekly
Time Frame
Average of week 1 and week 2 prior to treatment compared with the week 1 and week 2 during treatment
Title
Nepean Dyspepsia Index
Time Frame
Baseline NDI score (collected just prior to first dose) compared with End of Treatment NDI (collected just prior to last dose)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient meets ROME III criteria for functional dyspepsia (FD) Patient has a normal esophagogastroduodenoscopy (EGD) either during the Screening Period or within 2 years of the Screening Visit Patients who EITHER: Have not used a proton pump inhibitor (PPI) within 4 weeks of the Screening Visit, OR Have used a PPI at a stable dose for at least 4 weeks prior to the Screening Visit; Patient meets symptom severity criteria in the Pretreatment Period Patient is fluent and literate in Dutch, French, or English Exclusion Criteria: Patient meets criteria for gastroesophageal reflux disease (GERD, stable regimen of PPIs acceptable), constipation, diarrhea, lower abdominal pain, or gastroparesis Patient has a history of inflammatory bowel disease, chronic pancreatitis, small intestinal bacterial overgrowth, celiac disease, lactose intolerance, polycystic kidney disease, interstitial cystitis, or scleroderma Any significant neurological disease or a history of cancer (resected basal cell or squamous cell carcinoma of the skin is acceptable; complete remission of other cancers for 5 years or longer is also acceptable) History of active alcoholism or drug addiction within 12 months prior to the Screening Visit Hospitalized for a psychiatric condition or has made a suicide attempt during the two years before the Screening Visit Any organic or structural disease that can cause abdominal pain or discomfort
Facility Information:
Facility Name
AZ Sint-Lucas Brugge
City
Brugge
ZIP/Postal Code
8310
Country
Belgium
Facility Name
Antwerp University Hospital
City
Edegem
ZIP/Postal Code
2650
Country
Belgium
Facility Name
Z.O.L. - Campus St. Jan
City
Genk
ZIP/Postal Code
3600
Country
Belgium
Facility Name
Universitair Ziekenhuis Gent
City
Gent
ZIP/Postal Code
9000
Country
Belgium
Facility Name
UZ Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Facility Name
CHU Ambroise Pare
City
Mons
ZIP/Postal Code
7000
Country
Belgium
Facility Name
H. Hartziekenhuis Roselare-Menen vzw
City
Roselare
ZIP/Postal Code
8800
Country
Belgium
Facility Name
FlevoResearch
City
Almere
ZIP/Postal Code
1311 RL
Country
Netherlands
Facility Name
PreCare Trial and Recruitment
City
Beek
ZIP/Postal Code
6191 JW
Country
Netherlands
Facility Name
Andromed Breda
City
Breda
ZIP/Postal Code
4811 SW
Country
Netherlands
Facility Name
Andromed Eindhoven
City
Eindhoven
ZIP/Postal Code
5616GB
Country
Netherlands
Facility Name
Andromed Noord
City
Groningen
ZIP/Postal Code
9711 SG
Country
Netherlands
Facility Name
Andromed Leiden
City
Leiden
ZIP/Postal Code
2352 RA
Country
Netherlands
Facility Name
Maastricht University Med Ctr
City
Maastricht
ZIP/Postal Code
6229 HX
Country
Netherlands
Facility Name
Andromed Rotterdam
City
Rotterdam
ZIP/Postal Code
3021 HC
Country
Netherlands

12. IPD Sharing Statement

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Phase 2a Study of IW-9179 to Treat Functional Dyspepsia

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