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Secondary efficacy measures were inconsistent.
Secondary efficacy measures confirmed primary efficacy results.
Secondary efficacy and safety end points were also measured.
Secondary efficacy endpoint is a resolution of ABSSSI 7 to 14 days after completion of therapy.
Secondary efficacy parameters were pain intensity, pain duration and aura duration reduction.
The secondary efficacy endpoints showed no statistically significant differences between the two arms.
There were no statistically significant differences in any key secondary efficacy outcome between vortioxetine and placebo.
A positive treatment effect with entacapone was also seen with all secondary efficacy parameters, including QoL.
Secondary efficacy endpoints are the changes in UACR, serum cystatin C and serum creatinine from baseline.
The secondary efficacy variable was area under the curve (AUC) of FEV1.
Secondary efficacy endpoints were changes in FPG.
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