Confidence intervals vs. point estimators [Regulatives / Guidelines]
Dear ElMaestro
Thanks for these encouraging words!
No, that's not correct:
AUC:
Cmax:
Helmut suggested to cite the assessor in detail:
"The applicant's response does not resolve the objections concerning the bioequivalence issue. The first formulation of the Test product in the study showed bioinequivalence in comparison to the Reference product (Cmax outside of the widened acceptance range of 75-133%) and furthermore the values for the point estimates for the ratio of the geometric means (AUC0-t, AUC0-inf and Cmax) were all over 100%. Afterward the formulation of the Test product was changed and a new BE-study was conducted which again showed a bioinequivalence (AUC0-t and AUC0-inf outside of the acceptable range of 80-125%), with the point estimates all under 100%. The same test batch and the same formulation was investigated in a third BE-study, in which Cmax was out of the normally accepted range of 80-125% and all the point estimates were again over 100%, excluding the value 100% itself. Another batch of the same formulation of the Test product was then investigated in a fourth Replicate-BE-study which this time showed acceptable results for AUC0-t, AUC0-inf and Cmax (all in the normally acceptable range of 80-125%) but again the point estimates were only closely to 100%.
Even if it should be assumed that the first two BE-studies were only pilot studies and hence not suitable for statistical inclusion and taking into consideration that the formulation of the Test product was changed after the first BE-study, it still remains unclear why the same formulation of the Test product in the following three performed BE-studies shows varying values concerning point estimates in these studies (all values were lower, then higher and then again lower than 100% successively). This fluctuation can not be explained through the "intra-subject variability" as the latter influences Cmax and hence justifies the widening of the acceptance range for Cmax but not the fluctuating point estimates which are independent of this variability. This fluctuation is also independent of the number of subjects in the studies.
The Applicant is stating that the differences in point estimates in the four conducted BE-studies might result among others from different test batches. This is exactly the major objection raised by DE that the bioequivalence of the future batches of this formulation is not warranted."
Regards
Dan
❝ Honestly, I don't think you have wildly big a problem. I understand why the question is scary, but the task the assessor faces if he/she has to defend his/her views at CMD(h) is worse.
Thanks for these encouraging words!
❝ Do I get you correctly that there is no single point all four CI's have in common?
No, that's not correct:
AUC:
98.57-124.33%, 68.58-103.22%, 100.95-122.94%, 91.56-105.70%Cmax:
99.69-134.01%, 78.49-116.04%, 102.67-125.98%, 89.06-106.49%Helmut suggested to cite the assessor in detail:
"The applicant's response does not resolve the objections concerning the bioequivalence issue. The first formulation of the Test product in the study showed bioinequivalence in comparison to the Reference product (Cmax outside of the widened acceptance range of 75-133%) and furthermore the values for the point estimates for the ratio of the geometric means (AUC0-t, AUC0-inf and Cmax) were all over 100%. Afterward the formulation of the Test product was changed and a new BE-study was conducted which again showed a bioinequivalence (AUC0-t and AUC0-inf outside of the acceptable range of 80-125%), with the point estimates all under 100%. The same test batch and the same formulation was investigated in a third BE-study, in which Cmax was out of the normally accepted range of 80-125% and all the point estimates were again over 100%, excluding the value 100% itself. Another batch of the same formulation of the Test product was then investigated in a fourth Replicate-BE-study which this time showed acceptable results for AUC0-t, AUC0-inf and Cmax (all in the normally acceptable range of 80-125%) but again the point estimates were only closely to 100%.
Even if it should be assumed that the first two BE-studies were only pilot studies and hence not suitable for statistical inclusion and taking into consideration that the formulation of the Test product was changed after the first BE-study, it still remains unclear why the same formulation of the Test product in the following three performed BE-studies shows varying values concerning point estimates in these studies (all values were lower, then higher and then again lower than 100% successively). This fluctuation can not be explained through the "intra-subject variability" as the latter influences Cmax and hence justifies the widening of the acceptance range for Cmax but not the fluctuating point estimates which are independent of this variability. This fluctuation is also independent of the number of subjects in the studies.
The Applicant is stating that the differences in point estimates in the four conducted BE-studies might result among others from different test batches. This is exactly the major objection raised by DE that the bioequivalence of the future batches of this formulation is not warranted."
Regards
Dan
—
Kind regards and have a nice day
Dr_Dan
Kind regards and have a nice day
Dr_Dan
Complete thread:
- inter-batch variability? Dr_Dan 2010-08-04 10:29
- inter-batch variability? Pavidus 2010-08-04 11:57
- inter-batch variability? d_labes 2010-08-04 13:58
- inter-batch variability? ElMaestro 2010-08-04 17:09
- Between study variability common for HVDs Helmut 2010-08-04 19:45
- Between study variability common for HVDs ElMaestro 2010-08-04 21:01
- Representative batches? Helmut 2010-08-04 23:42
- Representative batches? ElMaestro 2010-08-05 08:40
- Representative batches? Helmut 2010-08-05 12:30
- Representative batches? Dr_Dan 2010-08-05 08:58
- Representative batches? Helmut 2010-08-05 12:45
- Confidence intervals vs. point estimators Dr_Dan 2010-08-06 09:55
- Confidence intervals vs. point estimators ElMaestro 2010-08-06 12:34
- Confidence intervals vs. point estimates Helmut 2010-08-06 13:20
- Confidence intervals vs. point estimatorsDr_Dan 2010-08-06 14:44
- Confidence intervals vs. point estimators ElMaestro 2010-08-06 15:01
- meta analysis? martin 2010-08-06 17:25
- meta analysis? ElMaestro 2010-08-06 17:57
- meta analysis? Helmut 2010-08-06 18:31
- meta analysis? Ohlbe 2010-08-06 23:21
- No chance against RMS? Dr_Dan 2010-08-10 12:27
- No chance against RMS? ElMaestro 2010-08-10 16:26
- No chance against RMS? Dr_Dan 2010-08-10 12:27
- meta analysis? ElMaestro 2010-08-06 17:57
- meta analysis? martin 2010-08-06 17:25
- Confidence intervals vs. point estimators ElMaestro 2010-08-06 15:01
- Confidence intervals vs. point estimators ElMaestro 2010-08-06 12:34
- Confidence intervals vs. point estimators Dr_Dan 2010-08-06 09:55
- Representative batches? Helmut 2010-08-05 12:45
- Representative batches? ElMaestro 2010-08-05 08:40
- Representative batches? Helmut 2010-08-04 23:42
- Between study variability common for HVDs ElMaestro 2010-08-04 21:01
- Batch-to-Batch Pharmacokinetic Variability kumarnaidu 2016-07-20 07:16
- tlast (Common) Helmut 2016-07-20 10:48
- tlast (Common) nobody 2019-02-21 15:20
- tlast (Common) ElMaestro 2019-02-21 16:32
- tlast (Common) nobody 2019-02-21 17:02
- tlast (Common) ElMaestro 2019-02-21 18:02
- tlast (Common) nobody 2019-02-21 18:17
- tlast (Common) ElMaestro 2019-02-21 18:02
- tlast (Common) nobody 2019-02-21 17:02
- tlast (Common) ElMaestro 2019-02-21 16:32
- tlast (Common) nobody 2019-02-21 15:20
- tlast (Common) Helmut 2016-07-20 10:48
- Between study variability common for HVDs Helmut 2010-08-04 19:45