Science fiction [Two-Stage / GS Designs]

posted by Helmut Homepage – Vienna, Austria, 2015-04-06 12:20 (2267 d 00:30 ago) – Posting: # 14662
Views: 14,756

Hi Mauricio,

» Are there any problem if, in the same protocol, replicated 4x2 and two-stage-design are considered?

A lot of problems. I agree with ElMaestro.

» For example, in first group were used 96 subjects on replicated (4x2) design with IC 95%. The result wasn't bioequivalent and the power was less than 80%.

Wow. I guess by “IC” you mean the GMR or T/R-ratio, right?* For FDA’s RSABE that would imply a CV of >361% and for EMA’s ABEL still a CV of >166%. What a nasty drug/formulation! BTW, for HVDs / HVDPs assuming a GMR of 95% is not a good idea. The two Lászlós recommend 90% – even if a “better” one was observed in a previous study.
You cannot simply assess the study for BE (α 0.05 or 90% CI) – that’s an add-on design, which was shown to inflate the TIE.1,2 In TSDs you have to use an adjusted α (at least if you proceed to the second stage).

» Therefore, a second group was added with 48 subjects, on replicated (4x2) design with the same IC 95%. In the end, first and second stage were combined and the result was bioequivalent …

… with a completely unknown type I error. If you used 0.05 already in the first stage you are dead.

» I am to consider this strategy because I don't know how much variability of drug is that!

Reference-scaling was developed to deal with the CV. If the CV turns out to be higher than expected you are allowed to scale more – and don’t loose too much power:



Problems arise not from the CV but from the GMR! BTW, most TSDs assume a fixed GMR. Full adaptive ones (i.e., adjusting for the observed GMR in the first stage) require a futility criterion and quite often are lacking power.2,3,4

» Is it possible?

Not yet – unless you have access to a massively parallel supercomputer. You would have to find a suit­able adjusted α and demonstrate beforehand that the overall type I error is maintained. Unlike in con­ventional (crossovers, parallel) designs due to the mixed-strategy (GMR-restriction of 0.80–1.25, no scaling at CV <30%; CVs >50% treated as if CV=50% for EMA) the power/sample-size estimation needs 105 simu­la­tions. Combine that with the 106 (slow convergence) needed to simulate the TIE in an entire grid of possible n1/CV-combinations. You’ll end up with 1013–1014 simulations…

Recently I faced an example where the sponsor (despite serious warnings of the CRO) insisted in a similar design. The sponsor is always right. :crying: A regulator asked for justification of the chosen α. I made a quick estimation (I have a very fast workstation): ~60 years running 24/7…
You don’t want to go there.

  1. Wonnemann M, Frömke C, Koch A. Inflation of the Type I Error: Investigations on Regulatory Recommendations for Bioequivalence of Highly Variable Drugs. Pharm Res. 2015;32(1):135–43. doi:10.1007/s11095-014-1450-z
  2. Schütz H. Two-stage designs in bioequivalence trials. Eur J Clin Pharmacol. 2015;71(3):271-81. doi:10.1007/s00228-015-1806-2
  3. Fuglsang A. Futility rules in bioequivalence trials with sequential designs. AAPS J. 2014;16(1):79–82. doi:10.1208/s12248-013-9540-0
  4. Kieser M, Rauch G. Two-stage designs for cross-over bioequivalence trials. Stat Med. 2015;34(16):2403–16. doi:10.1002/sim.6487

Dif-tor heh smusma 🖖
Helmut Schütz

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

Complete thread:

 Admin contact
21,530 posts in 4,499 threads, 1,523 registered users;
online 4 (0 registered, 4 guests [including 3 identified bots]).
Forum time: Sunday 12:51 UTC (Europe/Vienna)

Intellect distinguishes between the possible and the impossible;
reason distinguishes between the sensible and the senseless.
Even the possible can be senseless.    Max Born

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