A Study in Healthy Volunteers to Assess Safety and Blood Levels of AZD5847 After Multiple Doses Over 14 Days
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy
In brief
The purpose of this study is to determine the safety, tolerability and blood levels of AZD5847 after daily oral dosing for 14 days.
Key facts
- Study ID
- NCT01116258
- Run by
- AstraZeneca
- People needed
- 60
- Starts
- 2010-04-01
- Expected to finish
- 2010-10-01
- Last updated by the study team
- 2010-10-11
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- BMI between 18-30
You may not qualify if…
- Use of drugs that inhibit or induce cytochrome P450 3A4 enzymes
- History of presence of gastrointestinal, hepatic or renal disease
Where it is running
- Research Site — Overland Park, Kansas, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.