Research Site
Uppsala, Uppsala County, Sweden
NCT Number: NCT01239771
The purpose of the study is to assess safety, tolerability and pharmacokinetics of TC-5214 in medically stable elderly subjects following multiple oral doses.
Looking for future studies?
Notify Me65 year and older
All sexes
Interventional
Phase 1
Uppsala, Uppsala County, Sweden
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tablet 1, 2, or 4 mg of TC-5213 will be given twice daily for 4 days and once on the 5th day.
Two subjects in each cohort will be given placebo.
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
Time frame: Range of 5 days
AstraZeneca
Industry
A Phase I, Double-blind, Placebo-controlled, Parallel Group Study to Assess the Safety, Tolerability and Pharmacokinetics of TC-5214 Given as Multiple Ascending Oral Doses in Medically Stable Elderly Subjects
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.