NCT Number: NCT00055523
A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical Remission in Subjects With Crohn's Disease
Purpose of the study is to test whether adalimumab can induce clinical remission in subjects with active Crohn's disease when compared to placebo (an inactive substance)
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Conditions
Age range
18 year–75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Gastroenterology Associates of the East Bay, Berkeley, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion:
- Diagnosis of Crohn's disease
- CDAI score at baseline of between 220 and 450
- Normal laboratory parameters
- Willing and able to give informed consent
Exclusion:
- Diagnosis of ulcerative colitis
- Women cannot be pregnant or breastfeeding
- No previous use of infliximab or other anti-TNF antagonists
- No previous history of tuberculosis or listeria infection
- No previous history of cancer other than successfully treated skin cancer
Treatment and study plan
Primary outcomes
-
comparison of the induction of clinical remission
-
(achievement of a CDAI <150) of adalimumab 40 mg and 80 mg vs. placebo at Week 4.
Sponsors and collaborators
Lead sponsor
Abbott
Industry
Registry information
Official study title
A Phase II Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical Remission in Subjects With Crohn's Disease
Important dates
- Study start
- 2002
- First posted
- Mar 6, 2003
- Registry last updated
- Aug 15, 2006
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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