There is one clinical trial.
The primary purpose of this study is to assess the effect of food on the rate and extent of
absorption and the overall bioavailability of a single dose of CTx-1301 50 mg trimodal
tablets in healthy adult volunteers.
Primary Outcomes
Measure: Pharmacokinetic parameter (Cmax) Time: Hour 0 to hour 28
Measure: Pharmacokinetic parameter (AUC0-inf) Time: Hour 0 to hour 28
Measure: Pharmacokinetic parameter (AUC0-last) Time: Hour 0 to hour 28
Secondary Outcomes
Measure: Pharmacokinetic parameter (AUC0-3) Time: Hour 0 to hour 3
Measure: Pharmacokinetic parameter (AUC3-6) Time: Hour 3 to hour 6
Measure: Pharmacokinetic parameter (AUC6-9) Time: Hour 6 to hour 9
Measure: Pharmacokinetic parameter (AUC9-12) Time: Hour 9 to hour 12
Measure: Pharmacokinetic parameter (AUC12-16) Time: Hour 12 -16
Measure: Pharmacokinetic parameter K Time: Hour 0 to hour 28
Measure: Pharmacokinetic parameter T1/2 Time: Hour 0 to hour 28
Measure: Pharmacokinetic parameter Tmax Time: Hour 0 to hour 28
Measure: Pharmacokinetic parameter Tlag Time: Hour 0 to hour 28