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Study Evaluating Orally Administered ERB-041 in Subjects With Active Interstitial Cystitis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00275379
Recruitment Status : Withdrawn
First Posted : January 11, 2006
Last Update Posted : October 1, 2020
Information provided by (Responsible Party):
Wyeth is now a wholly owned subsidiary of Pfizer

Brief Summary:
This is a multicenter, randomized, double-blind, placebo-controlled, parallel-design, exploratory study of orally administered ERB-041 in subjects with active IC. The primary objectives of this study will be to investigate ERB-041's activity on levels of urinary APF, explore the gene expression response in peripheral blood mononuclear cells (PBMC), and to evaluate the safety of ERB-041 in women with active IC.

Condition or disease Intervention/treatment Phase
Cystitis, Interstitial Drug: ERB-041 Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, Exploratory Study of Orally Administered ERB-041 in Subjects With Active Interstitial Cystitis
Study Start Date : August 2006

Resource links provided by the National Library of Medicine

Primary Outcome Measures :
  1. Safety
  2. Levels of urinary antiproliferative factor (APF)
  3. Peripheral blood mononuclear cell (PBMC) gene expression profiles

Secondary Outcome Measures :
  1. Serum and urinary biomarkers of IC
  2. Clinical Activity:
  3. Global Response Assessment (GRA)
  4. O'Leary-Sant IC Symptom (ICSI) and Problem (ICPI) Index
  5. Pelvic Pain and Urinary/Frequency (PUF) Symptom Scale
  6. Female Sexual Function Index (FSFI)
  7. Voiding Diary

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Subjects seeking medical treatment for symptoms consistent with IC that have been ongoing for > 9 months or seeking medical treatment for a previous documented diagnosis of IC
  • Subjects who are not surgically sterile or postmenopausal (amenorrheic > 12 months) must agree and commit to the use of a medically acceptable, highly-effective (i.e. double-barrier or IUD), non-hormonal form of birth control during the study and for 30 days after the last dose of test

Exclusion Criteria:

  • Use of herbal supplements (except for a daily multivitamin/mineral supplement not containing herbal components)
  • History of cancer (other than resected cutaneous basal or squamous cell carcinoma or in situ cervical cancer) with less than 5 years documentation of a disease-free state
  • Vaginitis or vaginal infection within 1 month before randomization

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00275379

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United States, California
Glendora, California, United States, 91741
Redding, California, United States, 96001
San Diego, California, United States, 92103
United States, Florida
Aventura, Florida, United States, 33180
United States, Kansas
Kansas City, Kansas, United States, 66160
United States, Michigan
Jackson, Michigan, United States, 49201
United States, Oregon
Springfield, Oregon, United States, 97477
United States, Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Philadelphia, Pennsylvania, United States, 19140
Philadelphia, Pennsylvania, United States, 19146
United States, Texas
Houston, Texas, United States, 77030
Temple, Texas, United States, 76508
United States, Washington
Mountlake Terrace, Washington, United States, 98043
Baden, Austria, A-2500
Homburg/Saar, Germany, 66421
Munster, Germany, 48149
Sponsors and Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer
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Study Director: Medical Monitor Wyeth is now a wholly owned subsidiary of Pfizer
Principal Investigator: Trial Monitor For Germany, MedinfoDEU@wyeth.com
Principal Investigator: Trial Manager For Austria, WPVIMED@wyeth.com
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Responsible Party: Wyeth is now a wholly owned subsidiary of Pfizer
ClinicalTrials.gov Identifier: NCT00275379    
Other Study ID Numbers: 3142A4-109
B2381036 ( Other Identifier: Pfizer )
First Posted: January 11, 2006    Key Record Dates
Last Update Posted: October 1, 2020
Last Verified: September 2020
Keywords provided by Wyeth is now a wholly owned subsidiary of Pfizer:
Additional relevant MeSH terms:
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Cystitis, Interstitial
Urinary Bladder Diseases
Urologic Diseases