sterile saline for injection
Biological10mg/kg/dose sterile saline injected every other week for a total of 4 doses
NCT Number: NCT00656890
The purpose of this study is to determine the safety and tolerability of the MDX-1100 regimen in subjects with active Ulcerative colitis(UC) and determine the response rate at day 57 in patients administered MDX-1100.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Abbotsford British Columbia, British Columbia, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
10mg/kg/dose sterile saline injected every other week for a total of 4 doses
10mg/kg/dose MDX-1100 injected every other week for a total of 4 doses
Time frame: Day 57
Time frame: Day 57
Bristol-Myers Squibb
Industry
A Phase 2, Multi-dose, Double-blind, Placebo-controlled, Randomized, Multicenter Study of MDX-1100 (Anti-CXCL10 Human Monoclonal Antibody) in Subjects With Active Ulcerative Colitis
Acronym: MDX1100-06
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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