Getting variance components [🇷 for BE/BA]

posted by StatR – Turkey, 2017-02-08 09:41 (3054 d 09:46 ago) – Posting: # 17033
Views: 19,472

Hi again d_labes,

I tried to find the correct model by the post you referred.

❝ In the older package nlme / lme() you may formulate the model similar to the FDA code. See that post.


Unfortunately, I am confused after reading tons of post, and I could not figure out what is "trt", "tmt" ... Simply, my data is as follows

 Subject Formula Period Sequence     Yijk
       1       1      1        1 4.933014
       1       0      2        1 5.006829
       1       1      3        1 4.854162
       1       0      4        1 5.081755
       2       1      1        1 4.854738
       2       0      2        1 4.690311


Where Yijk is the PK characteristic. The first sequence represents "TRTR" and the second sequence: "RTRT". In the formula 1 = T and 0 = R. In the referred post you say that

model2 <- lme(y~ drug + prd + seq,
# this random statement fits a symmetric positive definite covariance matrix,
# identical to UN in SAS???
                random= ~ tmt-1|subj,
                #different within variabilities                 
                weights=varIdent(form = ~ 1 | drug),
                data=BlaBla, method="REML")


In your model y = Yijk, drug=Formula, prd=Period, seq=Sequence,
but what is tmt? Also, is the my data format correct for the lme? Or, Should I change Formula as 1 = T, 2 = R and Sequence as 1 = TRTR, 2 = RTRT? Could you please make me clear.

Best.

Complete thread:

UA Flag
Activity
 Admin contact
23,424 posts in 4,927 threads, 1,674 registered users;
49 visitors (0 registered, 49 guests [including 13 identified bots]).
Forum time: 20:27 CEST (Europe/Vienna)

Complex, statistically improbable things are by their nature
more difficult to explain than
simple, statistically probable things.    Richard Dawkins

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