2-stage design with interim sample size estimation [Two-Stage / GS Designs]

posted by d_labes  – Berlin, Germany, 2010-10-05 15:09  – Posting: # 5997
Views: 9,849

Dear all,

I have been questioned about the following design:

The sponsor/experimenter has no sufficient information about CV and point estimate ('true' value) to be able to make an "educated" guess of the sample size for a BE study. Some distinct shift in the point estimator is expected.

To save resources (its a fixed combination drug with 3 constituents, analytical expensive) he is not willing to do a pilot study and based on this a pivotal with BE decision not using the data from the pilot.

Thus the design shall be a 2-stage design. A first group of subjects (conception is 8-12) shall be dosed, analyzed and statistical evaluated. Based on the data (CV and point estimate) a final sample size shall be derived which will be utilized for the second stage.

There is the idea of a formal extreme small alpha to spend after the first stage =0.001 (to conform EMA guideline). This will ensure with great probability that the second stage will be reached. Practical no stopping will occur by that.

The only stopping rule is a maximum sample size constraint Nmax the sponsor is willing to fund. If the estimated sample size after stage 1 is greater the second stage will not performed.

Any body out there who knows how to handle such a design?
Is there something to do to protect the overall alpha (lower nominal alpha at second stage)?
Is the sample size estimation done as usually?

Any input will be highly appreciated.

Regards,

Detlew

Complete thread:

Activity
 Mix view
Bioequivalence and Bioavailability Forum |  Admin contact
19,818 posts in 4,201 threads, 1,361 registered users;
online 7 (0 registered, 7 guests [including 6 identified bots]).
Forum time (Europe/Vienna): 06:36 CEST

If I find 10,000 ways something won’t work, I haven’t failed.
I am not discouraged, because every wrong attempt discarded
is another step forward.    Thomas Alva Edison

The BIOEQUIVALENCE / BIOAVAILABILITY FORUM is hosted by
BEBAC Ing. Helmut Schütz
HTML5