The purpose of the study is to assess safety, tolerability and pharmacokinetics of TC-5214 in medically stable elderly subjects following multiple oral doses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
32
Research Site
Uppsala, Uppsala County, Sweden
Incidence of Adverse events
Time frame: Range of 5 days
Neurological examinations
Time frame: Range of 5 days
Visual acuity tests
Time frame: Range of 5 days
Vital signs
Time frame: Range of 5 days
Physical examinations
Time frame: Range of 5 days
Laboratory parameters
Time frame: Range of 5 days
Suicidality as assessed by the Columbia-Suicide Severity Rating Scale
Time frame: Range of 5 days
Electrocardiograms
Time frame: Range of 5 days
Pharmacokinetic variables of TC-5214 by assessment of drug concentrations in plasma
Time frame: Range of 5 days
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