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In this work, the effectiveness of this dosing sequence and its reversed dosing sequence was compared through electrophoretic mobility and colloidal stability studies.
There was also no significant effect of dosing sequence.
Similarly, there was no significant effect of dosing sequence.
There was no significant effect of dosing sequence on object recognition accuracy.
There was no significant effect of dosing sequence or days elapsed since last exposure to an MDMA-like drug.
In order to control for possible sequence effects, linear models initially included a dummy-coded term for dosing sequence and a sequence-condition interaction term.
Similar(39)
Fifteen healthy subjects were randomized to 1 of 3 dosing sequences, with five subjects per sequence: oral placebo, CC-930 75 mg QD, or CC-930 200 mg QD for 6 days.
In the combination treatment, two dosing sequences were used: TAA and ATA (as above).
Three alternate dosing sequences were used during cycle 1 to examine dynamic changes in molecular profiles.
To facilitate tissue sampling for biomarker analyses in the present trial, we used three dosing sequences in cycle 1 only.
Subjects (N = 24) were randomly assigned to one of four dosing sequences: ABCD, BDAC, CADB, and DCBA.
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