Sas proc mixed and 4 period partial replicate Cross over [Design Issues]

posted by M.tareq  – 2016-05-03 13:35 (3707 d 14:38 ago) – Posting: # 16266
Views: 10,786

Hello, can any one please guide me on performing stat analysis of a 4 period 4 seq 3 treatment partial replicate Cross over study, where the ref product only replicate against t1 and t2 for a bioequivlence study of sofosbuvir?
The FDA recommendation is for full replicate and there are little information found regarding a 4 period Cross over with partial replication?
What other effects to account for beside the usual fixed effects in traditional 2x2 Cross over?
Within subject effect, within formulation variability, and carry over effect?
Thanks in advance


Newbie in stat...


Edit: Category changed; see also this post #1. [Helmut]

Complete thread:

UA Flag
Activity
 Admin contact
23,655 posts in 4,993 threads, 1,572 registered users;
364 visitors (0 registered, 364 guests [including 36 identified bots]).
Forum time: 04:14 CEST (Europe/Vienna)

The real struggle is not between the right and the left
but between the party of the thoughtful
and the party of the jerks.    Jimmy Wales

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5