Sereng ☆ USA, 2022-05-12 19:17 (1007 d 16:57 ago) Posting: # 22975 Views: 2,823 |
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Dear Colleagues, despite best efforts (adequate sampling duration), if you should determine that one or more subjects contributes a large extrapolated AUC (>20%) in a BE study, how should we deal with it? Regards, — Biostatistically Challenged CEO |
mittyri ★★ Russia, 2022-05-15 00:06 (1005 d 12:09 ago) @ Sereng Posting: # 22986 Views: 2,346 |
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Hi Sereng, ❝ despite best efforts (adequate sampling duration), if you should determine that one or more subjects contributes a large extrapolated AUC (>20%) in a BE study, how should we deal with it? that's OK if the number of subjects with large residual area is less than 20% Otherwise the sampling duration is not adequate or there are other issues with formulation/analyte/product PS: above is true for EMA guide and bound jurisdictions — Kind regards, Mittyri |
Sereng ☆ USA, 2022-05-18 07:59 (1002 d 04:16 ago) @ mittyri Posting: # 22999 Views: 2,332 |
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Many thanks! — Biostatistically Challenged CEO |
Helmut ★★★ ![]() ![]() Vienna, Austria, 2022-05-23 13:43 (996 d 22:32 ago) @ Sereng Posting: # 23011 Views: 2,156 |
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Hi Sereng, ❝ […] if […] one or more subjects contributes a large extrapolated AUC (>20%) in a BE study, how should we deal with it? Since you posted in the -category: Contrary to the EMA* (and most other jurisdictions), in none of the FDA’s guidances a ‘rule’ like AUC0–t ≥ 80% of AUC0–∞ is mentioned. Only that […] sampling should continue for at least three or more terminal elimination half-lives of the drug. If you decide to follow the ‘80% rule’, state in the protocol that the respective subject(s) will be excluded from the comparison of AUCs but kept for the comparison of Cmax. Since Cmax is in general more variable than the AUCs, likely you based your sample size on it. Hence, excluding subjects from the comparison of AUCs is expected to have a limited effect on power. An example for a 2×2×2 design, target power 80%, different CVs (Cmax > AUC0–∞ > AUC0–t) and T/R-ratios in
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