Nonbinding futility rule [Two-Stage / GS Designs]

posted by d_labes  – Berlin, Germany, 2018-06-14 10:47 (1517 d 12:20 ago) – Posting: # 18906
Views: 13,899

(edited by d_labes on 2018-06-14 10:58)

Dear Ben,

» The reference at page 19 actually refers to the CI futility criterion,

I know.

» ... in my opinion the only possibility is: if you want to be able to handle it in a nonbinding manner, then you have to go with conditional error rates only (i.e. you cannot use the estimated conditional target power as target power for calculation of n2). So, we would need to select ssr.conditional = "error".

My first thought was: Set fCpower = 1, that results in do not use the power futility criterion. This gives n2=16 for mittyri's example, CV1=0.2575165, n1=38, fCpower=1).

Your suggestion, CV1=0.2575165, n1=38, ssr.conditional = "error")
gives also n2=16. Astonishing or correct?

Avoiding the conditional sample size re-estimation, i.e. using the conventional sample size re-estimation via, CV1=0.2575165, n1=38, ssr.conditional = "no")
gives n2=4. Ooops? Wow!

Helmuts caveat of how to decide in case of "nonbinding futility" needs to be considered, scientifically, not via NLYW :-D.
IIRC the term "nonbinding" in the context of sequential designs is used for flexibility in stopping or continuing due to external reasons. Do we have such here?

Binding, nonbinding - does it have an impact on the alpha control? I think not, but are not totally sure.



Complete thread:

UA Flag
 Admin contact
22,289 posts in 4,666 threads, 1,585 registered users;
online 6 (0 registered, 6 guests [including 3 identified bots]).
Forum time: Tuesday 23:08 CEST (Europe/Vienna)

The existing scientific concepts cover always only
a very limited part of reality,
and the other part that has not yet
been understood is infinite.    Werner Heisenberg

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