A Single Dose Study to Assess the Safety, Effects, and Blood and Urine Drug Levels of AZD3293 in Healthy Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy Young Volunteers, Healthy Elderly Volunteers
In brief
This is a single dose study in healthy male and female (of non-child bearing potential) volunteers, to assess the safety, effects on the body, and blood and urine drug levels of AZD3293. AZD3293 is being developed for the treatment of Alzheimer's Disease
Key facts
- Study ID
- NCT01739647
- Run by
- AstraZeneca
- People needed
- 72
- Starts
- 2012-12-01
- Expected to finish
- 2013-05-01
- Last updated by the study team
- 2013-08-27
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male and female (of non-childbearing potential) subjects
- Body mass index (BMI) between 19 and 30 kg/m2 and weigh at least 50 kg and no more than 100 kg
You may not qualify if…
- History or presence of psychiatric disease/condition, GI, renal, hepatic, cardiovascular, psychiatric, or retinal diseases or disorders
- History of neurological disease, including seizures, recent memory impairment, or clinically significant head injury
- History of use of antipsychotic drugs , or chronic use of antidepressant or anxiolytic drugs
- Frequent use (more than 2 days per week during the last 12 weeks) of tobacco or other nicotine products
Where it is running
- Research Site — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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