NCT Number: NCT00101946
Nine-Weeks Treatment With 683699 In Subjects With Moderately-To-Severely Active Crohn's Disease
This study will evaluate the effectiveness and safety of the investigational drug 683699 in treating subjects with moderately to severely active CD (Crohn's Disease).
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
GSK Investigational Site, Calgary, Alberta, Canada
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Diagnosed with CD and reconfirmed in previous 2 years by a radiologic or endoscopic assessment including histology.
- CDAI (Crohn's Disease Activity Index) score of 220-450 after 1 week of screening.
- CRP (C-Reactive Protein) level of >4mg at screening.
Exclusion criteria
- Significantly abnormal laboratory tests or ECG (electrocardiogram) results.
- Current use of an elemental diet or parenteral nutrition.
- Clinically significant positive stool culture.
- Ongoing neoplastic disease of the bowel.
- Bowel perforation other than fistulae.
- Has an ileostomy or colostomy.
- Fixed symptomatic gastrointestinal (GI) stricture within 6 months or obstructive symptoms within 3 months of screening.
- Any bowel resection within 12 months of screening or bowel resection without subsequent demonstration of recurrence of active CD.
- More than 100cm of bowel resected.
- Non-curative bowel surgery with 2 months of screening.
- Symptoms attributed to short bowel syndrome.
- Uncontrolled bacterial, viral, or fungal infection or congenital or acquired immunodeficiency.
- Women who are pregnant, breast feeding, or planning to become pregnant during the study.
Permitted medications:
- Less than or equal to 20mg/day oral corticosteroids for at least 4 weeks prior to screening and on stable doses for 2 weeks prior to screening.
- Azathioprine and 6-MP (6-Mercaptopurine) stable dose for 3 months prior to screening.
- 5-ASA (5-Aminosalicylic acid) stable dose for 1 month prior to screening.
Prohibited medications:
- Greater than 20mg/day oral corticosteroids, or systemic intravenous corticosteroids, or antibiotics as a treatment for CD within 4 weeks prior to screening.
- Cyclosporine or methotrexate during the 2 months prior to screening.
- Infliximab or other biological treatments within 3 months prior to screening.
Treatment and study plan
Primary outcomes
-
Proportion of subjects who are responders at Week 6.
Secondary outcomes
-
- Proportion of subjects with response at other timepoints. - Proportion of subjects in remission. - Average rate of response for the CDAI score. - Mean change from baseline in CDAI score Improvement in Quality of Life.
Sponsors and collaborators
Lead sponsor
GlaxoSmithKline
Industry
Registry information
Official study title
A Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Investigate the Efficacy and Safety of Nine-weeks Administration of Three Doses of SB-683699 in Subjects With Moderately to Severely Active Crohn's Disease
Important dates
- Study start
- 2004
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Jan 19, 2005
- Registry last updated
- Apr 13, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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