Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 181 in Healthy Subjects and Subjects With Mild to Moderate Ulcerative Colitis
Stopped early · Phase 1
Conditions studied: Ulcerative Colitis
In brief
To assess the safety and tolerability of single subcutaneous (SC) and intravenous (IV) doses of AMG 181 in healthy subjects and of a single SC dose in subjects with mild to moderate ulcerative colitis (UC)
Key facts
- Study ID
- NCT01164904
- Run by
- Amgen
- People needed
- 72
- Starts
- 2010-07-01
- Expected to finish
- 2013-03-01
- Last updated by the study team
- 2013-07-25
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
Where it is running
- Research Site — Glendale, California, United States
- Research Site — Danbury, Connecticut, United States
- Research Site — Plymouth, Minnesota, United States
- Research Site — Duncansville, Pennsylvania, United States
- Research Site — Herston, Queensland, Australia
- Research Site — Adelaide, South Australia, Australia
- Research Site — Prahran, Victoria, Australia
- Research Site — Nedlands, Western Australia, Australia
- Research Site — Auckland, New Zealand
- Research Site — Christchurch, New Zealand
Full record on ClinicalTrials.gov
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