Open your mouth and forcefully spit the water out [Two-Stage / GS Designs]

posted by Helmut Homepage – Vienna, Austria, 2013-10-18 15:29 (4629 d 08:43 ago) – Posting: # 11695
Views: 29,989

Hi Shuanghe,

❝ Q: "..., we'd like to ask about the current status of 2-stage design BE study, ... if the BE protocol with Potvin's Method C is acceptable now ..."


❝ A: "Potvin's methods are not acceptable in EMA."


Simply mad. And I don’t mean the MAD.
Have you asked them which methods would be acceptable according to their impeccable wisdom instead? They should enlighten us simpletons.

❝ so, first question, how could it be? Have some of you guy's dossiers with Potvin's method(s) been approved/accepted (no deficient letter, rejection letter etc)?


Yes. For some recent (this year’s) experiences see slide 45 of this presentation. Method C [sic] accepted by Germany (RMS) and CMSs Austria, Denmark, Sweden, and The Netherlands. Spain asked for an all-fixed effects analysis (subjects within sequence were random in the original analysis).
Note that in a previous case (slide 44) MEB didn’t like intermediate power.

❝ I always had the impression that method B is practically mentioned in the guide. Not quite. :no: There's no mention of interim power analysis in the BE guide while method B... you know. So I guess the power analysis is probably the "evil" here causing all the fuss...


Maybe. I suspect the guys writing the GL failed to comprehend the published methods, which – with no exception! – depend on an intermediate power estimation step. I hope someone has the balls and goes for a referral. If a GL (not a law anyway) states 2×2=5 I would wholeheartedly ignore it for sure.

BTW, the additional term introduced in the Q&A Ref.7 is futile as well. I have heard that this section was excreted by EMA’s Biostatistical Working Party and the PK Working Party is just “hosting” it. What the heck? A paper “On the Statistical Model of the Two-Stage Design in Bioequivalence Assessment” by Karalis/Macheras is currently under review (J Pharm Pharmacol). From their key findings:

The overall performance in terms of % BE acceptance is identical. The additional term, ‘Sequence × Stage’, suggested in the EMA method is in most cases non-signi­fi­cant. The same results were obtained regardless of the type (fixed or random) of the effect applied to the ‘Subjects’ term.

And the conclusions:

Any BE study either finished or in progress which relies on the existing literature methodology leads to the same % BE acceptance as if it was analyzed with the recently proposed EMA method.

So what?

❝ There's rumour that some working party is currently discussing this topic. Anyone has any insight?


Not me.

Dif-tor heh smusma 🖖🏼 Довге життя Україна! [image]
Helmut Schütz
[image]

The quality of responses received is directly proportional to the quality of the question asked. 🚮
Science Quotes

Complete thread:

UA Flag
Activity
 Admin contact
23,655 posts in 4,993 threads, 1,571 registered users;
137 visitors (0 registered, 137 guests [including 9 identified bots]).
Forum time: 00:12 CEST (Europe/Vienna)

Science is simply common sense at its best that is,
rigidly accurate in observation, and
merciless to fallacy in logic.    Thomas Henry Huxley

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