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

posted by M.tareq  – 2016-05-03 13:35 (3348 d 20:42 ago) – Posting: # 16266
Views: 9,647

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
23,427 posts in 4,929 threads, 1,679 registered users;
92 visitors (0 registered, 92 guests [including 56 identified bots]).
Forum time: 10:18 CEST (Europe/Vienna)

Half the harm that is done in this world
Is due to people who want to feel important.    T. S. Eliot

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