sury ☆ India, 20190416 06:44 Posting: # 20171 Views: 1,021 

Hii All... Anyone know about the sample size estimation for the non inferiority clinical trials, as per the literatures and some google says to consider the NI Margin to some percentage and estimate the sample size I have tried to do the same in FARTSSIE23 (Noninferiority, Parallel), but in addition to that Standard deviation is necessary for the same and in SAS (PROC POWER), we need to provide the CV to estimate the sample size Can we assume the standard deviation or we need to provide the exact Standard deviation (obtained from the literatures on the drug) ? Dose the same criteria applicable as that of the ISCV concept for the bio equivalence studies? Best Regards... Edit: Category changed; see also this post #1. [Helmut] 
Helmut ★★★ Vienna, Austria, 20190416 14:53 @ sury Posting: # 20175 Views: 888 

Hi Sury, » […] sample size estimation for the non inferiority clinical trials […] I have tried to do the same in FARTSSIE23 (Noninferiority, Parallel), but in addition to that Standard deviation is necessary for the same and in SAS (PROC POWER), we need to provide the CV to estimate the sample size No idea about Proc Power . Let’s try the example of FARTSSIE2.4 (which is based on Julious’ Example 4.1.1.1.*) in PowerTOST :
» Can we assume the standard deviation … Sure. » … or we need to provide the exact Standard deviation (obtained from the literatures on the drug) ? That’s also an estimate. The true value is unknown. » Dose the same criteria applicable as that of the ISCV concept for the bio equivalence studies? Not sure what you mean here. Can you try to explain?
— Cheers, Helmut Schütz The quality of responses received is directly proportional to the quality of the question asked. ☼ Science Quotes 
sury ☆ India, 20190417 04:55 @ Helmut Posting: # 20180 Views: 840 

Hello » » Can we assume the standard deviation … » » Sure. » » » … or we need to provide the exact Standard deviation (obtained from the literatures on the drug) ? » » That’s also an estimate. The true value is unknown. » » » Dose the same criteria applicable as that of the ISCV concept for the bio equivalence studies? » » Not sure what you mean here. Can you try to explain? I mean to say is in normal bio equivalence studies, we need the ISCV information in order to estimate the sample size. Does this same criteria is applicable for the standard deviation for Noninferiority Trails too?. but i got my answer in the above explanation.. And in addition to that i have one more doubt... By the above explanation, we dont need any sort of information regarding the drug nature or literature support or pilot studies for the estimation of the sample size? In general BE studies, we require the pilot study or literature support for the sample size estimation (ISCV) for the pivotal studies. As we are assuming the margin of error, Standard deviation and the power (Which are required) for the non inferiority trials Correct me if i am wrong anywhere BTW, Thanks for your reply. it made me clear about the concept on Noninferiority trials. Edit: Full quote removed. Please delete everything from the text of the original poster which is not necessary in understanding your answer; see also this post #5! [Helmut] 
Helmut ★★★ Vienna, Austria, 20190417 08:59 @ sury Posting: # 20181 Views: 811 

Hi Sury, first of all, please delete everything from the text of the original poster which is not necessary in understanding your answer; see also this post #5! We edited 80% of your replies. Hence, this is the first warning. » » » Can we assume the standard deviation … » » Sure. » » » … or we need to provide the exact Standard deviation (obtained from the literatures on the drug) ? » » That’s also an estimate. The true value is unknown. » » » Dose the same criteria applicable as that of the ISCV concept for the bio equivalence studies? » » Not sure what you mean here. Can you try to explain? » » I mean to say is in normal bio equivalence studies, we need the ISCV information in order to estimate the sample size. Does this same criteria is applicable for the standard deviation for Noninferiority Trails too?. but i got my answer in the above explanation.. No, you got it wrong. You can assume something but with a reason! » By the above explanation, we dont need any sort of information regarding the drug nature or literature support or pilot studies for the estimation of the sample size? Are you kidding? You will administer a drug to healthy volunteers or patients which always carries some risk. Don’t play games. » In general BE studies, we require the pilot study or literature support for the sample size estimation (ISCV) for the pivotal studies. » » As we are assuming the margin of error, Standard deviation and the power (Which are required) for the non inferiority trials » » Correct me if i am wrong anywhere Almost everywhere. » it made me clear about the concept on Noninferiority trials. Sorry, you got me wrong. The Forum’s Policy states “We expect a basic knowledge of BE/BA or related fields …” – which you are lacking. You shouldn’t rely on anything you find on the internet (including this forum) without a basic understanding. I strongly recommend to read textbooks on the topic. See this post (always get the latest editions). #1, #3, #11 are good entry points. For sample size estimation additionally:
— Cheers, Helmut Schütz The quality of responses received is directly proportional to the quality of the question asked. ☼ Science Quotes 