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Therapeutic Study of ONO-4819CD for Ulcerative Colitis

Primary Purpose

Ulcerative Colitis

Status
Terminated
Phase
Phase 2
Locations
Japan
Study Type
Interventional
Intervention
Rivenprost (drug)
Sponsored by
Kyoto University, Graduate School of Medicine
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis focused on measuring Ulcerative colitis, EP4 agonist, PGE2

Eligibility Criteria

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

Inclusion Criteria: Clinical diagnosis of ulcerative colitis Mild to moderate ulcerative colitis refractory to 5-aminosalicylates therapy. 20 years and above Must obtain written informed consent Exclusion Criteria: Corticosteroids therapy within two weeks before enrollment Immunosuppressive therapy within three months before enrollment Leukocytapheresis therapy within one month before enrollment Blood transfusion within two weeks before enrollment Impaired renal function Impaired hepatic function Uncontrolled hypertension/hypotension Uncontrolled arrhythmia Impaired cardiac function Cancer Uncontrolled diabetes Interstitial pneumonia Glaucoma History of colon resection Infectious diseases needing medical treatments Drug allergy Pregnancy

Sites / Locations

  • Kyoto University, Graduate School of Medicine

Outcomes

Primary Outcome Measures

Remission evaluated by DAI scores at 14 and 28 days

Secondary Outcome Measures

Improvement by DAI scores; Change in DAI scores; CAI scores at 3, 7, 14 and 28 days; Colonoscopic and histopathological scores at 14 and 28 days; Clinical severity and symptom scores at 7, 14 and 28 days; Cytokines at 7, 14 and 28 days; Adverse effects.

Full Information

First Posted
February 24, 2006
Last Updated
April 27, 2009
Sponsor
Kyoto University, Graduate School of Medicine
Collaborators
National Institute of Biomedical Innovation
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1. Study Identification

Unique Protocol Identification Number
NCT00296556
Brief Title
Therapeutic Study of ONO-4819CD for Ulcerative Colitis
Official Title
A Randomized, Placebo-Controlled Trial of ONO-4819CD for Treatment of Mild to Moderate Ulcerative Colitis.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2009
Overall Recruitment Status
Terminated
Why Stopped
terminated
Study Start Date
February 2006 (undefined)
Primary Completion Date
December 2007 (Anticipated)
Study Completion Date
March 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Kyoto University, Graduate School of Medicine
Collaborators
National Institute of Biomedical Innovation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to investigate whether ONO-4819CD is safe and effective in the treatment of mild to moderate ulcerative colitis.
Detailed Description
Ulcerative colitis is a relapsing disease of unknown cause characterized by bloody diarrhea. Therapy usually involves 5-aminosalicylates, corticosteroids and immunosuppressants. However, steroid resistance and dependency can become problematic. Immunosuppressive drugs, such as azathioprine, are beneficial but may have serious side effects. Therefore, new therapeutic approach is needed. Prostaglandin E2 is one of the prostanoids, which is involved with innate immunity. PGE2 induces oral tolerance to specific antigen in the small intestine and downregulates the production and release of proinflammatory cytokines by macrophages and neutrophils. Accordingly, PGE2 is considered to be the mediator of mucosal protection. Recently, it was elucidated that disruption of EP4 gene, which is one of PGE receptors, caused severe colitis in mice. Moreover, EP4-selective agonist (AE1-734) was also revealed to ameliorate severe dextran sodium sulfate-induced colitis in mice. We therefore examined the effects of 2 weeks intravenous EP4-selective agonist therapy for patients with mild to moderate ulcerative colitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
Keywords
Ulcerative colitis, EP4 agonist, PGE2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Rivenprost (drug)
Primary Outcome Measure Information:
Title
Remission evaluated by DAI scores at 14 and 28 days
Secondary Outcome Measure Information:
Title
Improvement by DAI scores; Change in DAI scores; CAI scores at 3, 7, 14 and 28 days; Colonoscopic and histopathological scores at 14 and 28 days; Clinical severity and symptom scores at 7, 14 and 28 days; Cytokines at 7, 14 and 28 days; Adverse effects.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of ulcerative colitis Mild to moderate ulcerative colitis refractory to 5-aminosalicylates therapy. 20 years and above Must obtain written informed consent Exclusion Criteria: Corticosteroids therapy within two weeks before enrollment Immunosuppressive therapy within three months before enrollment Leukocytapheresis therapy within one month before enrollment Blood transfusion within two weeks before enrollment Impaired renal function Impaired hepatic function Uncontrolled hypertension/hypotension Uncontrolled arrhythmia Impaired cardiac function Cancer Uncontrolled diabetes Interstitial pneumonia Glaucoma History of colon resection Infectious diseases needing medical treatments Drug allergy Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shuh Narumiya, MD, PhD
Organizational Affiliation
Kyoto University, Graduate School of Medicine
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tsutomu Chiba, MD, PhD
Organizational Affiliation
Kyoto University, Graduate School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kyoto University, Graduate School of Medicine
City
Kyoto
ZIP/Postal Code
606-8501
Country
Japan

12. IPD Sharing Statement

Citations:
PubMed Identifier
11927615
Citation
Kabashima K, Saji T, Murata T, Nagamachi M, Matsuoka T, Segi E, Tsuboi K, Sugimoto Y, Kobayashi T, Miyachi Y, Ichikawa A, Narumiya S. The prostaglandin receptor EP4 suppresses colitis, mucosal damage and CD4 cell activation in the gut. J Clin Invest. 2002 Apr;109(7):883-93. doi: 10.1172/JCI14459.
Results Reference
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PubMed Identifier
9124591
Citation
Morimoto K, Sugimoto Y, Katsuyama M, Oida H, Tsuboi K, Kishi K, Kinoshita Y, Negishi M, Chiba T, Narumiya S, Ichikawa A. Cellular localization of mRNAs for prostaglandin E receptor subtypes in mouse gastrointestinal tract. Am J Physiol. 1997 Mar;272(3 Pt 1):G681-7. doi: 10.1152/ajpgi.1997.272.3.G681.
Results Reference
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Therapeutic Study of ONO-4819CD for Ulcerative Colitis

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