This study will evaluate the safety, blood levels, and effects of TRV130A on pain perception and sedation in healthy adult males.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
74
Intravenous infusion of 1 hour duration
Intravenous infusion of 1 hour duration
ICON Development Solutions
Omaha, Nebraska, United States
Number of subjects with adverse events
Time frame: Baseline to 8 days after dose administration
Area under the plasma concentration versus time curve of TRV130A
Time frame: Baseline to 24 hours after dose administration
Effect of TRV130A on pain perception using cold pain test
Time frame: Baseline to 3 hours after dose administration
Effect of TRV130A on pupil diameter
Time frame: Baseline to 3 hours after dose administration
Effect of TRV130A on eye movements
Using saccadic eye movement measurement
Time frame: Baseline to 3 hours after dose administration
Effect of TRV130A on sedation
Sedation evaluated by questionnaire
Time frame: Baseline to 3 hours after dose administration
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