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Study Evaluating ERB-041 in Active Crohn's Disease

This study is ongoing, but not recruiting participants.

Sponsored by: Wyeth
Information provided by: Wyeth
ClinicalTrials.gov Identifier: NCT00245947
  Purpose

Evaluate the response of inflammatory serum markers to oral ERB-041 in subjects with inflammation associated with active Crohn’s disease.


Condition Intervention Phase
Crohn's Disease
Drug: ERB-041
Phase I

Genetics Home Reference related topics:   Crohn disease   

MedlinePlus related topics:   Crohn's Disease   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title:   A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel- Design, Exploratory Pharmacogenomic, Safety and Activity Study of Orally Administered ERB-041 in Subjects With Inflammation Associated With Active Crohn’s Disease

Further study details as provided by Wyeth:

Primary Outcome Measures:
  • Inflammatory serum markers
  • Pharmacogenomics
  • Safety

Secondary Outcome Measures:
  • Crohn's Disease Activity Index (CDAI) scores.
  • Cell surface markers
  • Fecal markers

Estimated Enrollment:   48
Study Start Date:   April 2004

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Men and women, minimum 18 years of age with a diagnosis of Crohn’s disease greater than 3 months,
  • Eligible subjects must have adequate hematologic, renal, and hepatic function.

Other inclusions apply

Exclusion Criteria:

  • Use of the following medications within the specified time period before randomization is prohibited:

Within 48 hours before randomization

  • Nonsteroidal antiinflammatory drugs (NSAIDs) Within 2 weeks before randomization
  • Herbal supplements (except for a daily multivitamin/mineral supplement not containing herbal components).

Other exclusions applies

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00245947

Sponsors and Collaborators
Wyeth

Investigators
Study Director:     Medical Monitor     Wyeth    
  More Information


Study ID Numbers:   3142A3-102
First Received:   October 26, 2005
Last Updated:   May 18, 2006
ClinicalTrials.gov Identifier:   NCT00245947
Health Authority:   United States: Food and Drug Administration

Keywords provided by Wyeth:
Crohn's Disease  
Inflammation  

Study placed in the following topic categories:
Digestive System Diseases
Gastrointestinal Diseases
Crohn Disease
Inflammatory Bowel Diseases
Gastroenteritis
Intestinal Diseases
Inflammation

ClinicalTrials.gov processed this record on November 04, 2008




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