Posting: # 19654
I am new comer on this forum working in bio equivalence department so I just wanted to know that If we got larger difference between 90% CI limit for any primary factor like AUC0-t, AUC 0-infinity or Cmax e.g. lower limit is 90% and upper limit is 120% so what could be the predictions about the factors that widen the limit (both factor in vitro or in vivo).
Response will be highly appreciated
Edit: category changed [Ohlbe]
@ mirza baig
Posting: # 19655
Dear mirza baig,
» I am new comer on this forum
» If we got larger difference between 90% CI limit for any primary factor like AUC0-t, AUC 0-infinity or Cmax e.g. lower limit is 90% and upper limit is 120% so what could be the predictions about the factors that widen the limit (both factor in vitro or in vivo).
First, I would clarify that getting a result of 90-120 % is not something abnormal. I would actually be more uneasy to see something like 99-103 %.
Basically, the main factor will be the number of subjects in your study and how good your assumptions on intra-subject variability were when you calculated the number of subjects required...
I will try and explain simply, but I would suggest you to take a look at Helmut's lectures on BE, and more specifically on sample size calculations.
So first, the width of the 90 % confidence interval depends on the intra-subject variability of the PK parameters (Cmax and AUC). This variability is a characteristic of the molecule that you study (some molecules have a low variability, some have a large variability). It can be increased by external factors: first the formulation you are studying (a bad formulation can increase the variability - and sometimes the reference product is the one that has a poor formulation, not the generic !), food (fasted vs. fed), and how well your study was standardised. The higher the intra-subject CV, the wider the 90 % CI.
The other factor that directly influences the width of the 90 % CI is the number of subjects in your study. You will get a narrower 90 % CI with 48 subjects than with 24.
When you write the protocol of the study, you have to calculate the number of subjects you will enrol. The calculation takes the following into consideration:
When they are missing data on the intra-CV, some people will just play it quick and dirty: they will write some value and a number of subjects in the protocol, depending on how much the sponsor is ready to pay. That's clearly unethical. If the variability is higher, your study will be under-powered and will fail, and you will have exposed the subjects to the drug unnecessarily. If the variability is lower, your study will be overpowered and you will have exposed too many subjects.
Keep in mind also that Cmax and AUC have a different variability. You have to use the largest of the two to calculate the number of subjects needed.
So now back to your question regarding the width of the 90 % CI at the end of your study. If you get a very narrow 90 % CI, it may be because: