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| Sponsor: | Wyeth |
|---|---|
| Information provided by: | Wyeth |
| ClinicalTrials.gov Identifier: | NCT00038922 |
Purpose
To explore the safety of orally delivered rhIL-11 in patients with mild to moderate left-sided ulcerative colitis.
To explore the effects of orally administered rhIL-11 on pharmacogenomics in blood samples and in colonic biopsy tissue samples.
| Condition | Intervention | Phase |
|---|---|---|
|
Ulcerative Colitis Inflammatory Bowel Disease |
Drug: rhIL-11 |
Phase I |
| Study Type: | Interventional |
| Study Design: | Treatment |
| Official Title: | A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Escalating, Safety and Exploratory Pharmacogenomic Study of Orally Administered Recombinant Human Interleukin Eleven (rhIL-11) in Patients With Mild to Moderate Left-Sided Ulcerative Colitis |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | 3067K5-114 |
| Study First Received: | June 5, 2002 |
| Last Updated: | May 17, 2006 |
| ClinicalTrials.gov Identifier: | NCT00038922 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Left-Sided Ulcerative Colitis |
|
Gastrointestinal Diseases Antineoplastic Agents Ulcer Colonic Diseases Inflammatory Bowel Diseases Colitis, Ulcerative Intestinal Diseases |
Pharmacologic Actions Digestive System Diseases Pathologic Processes Oprelvekin Therapeutic Uses Gastroenteritis Colitis |