Mithu
★    

India,
2023-05-04 06:59
(212 d 09:58 ago)

Posting: # 23541
Views: 1,149
 

 505 b(2) application & requirement of bio­equi­va­lence [Regulatives / Guidelines]

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Hello All,


My question is, "is it mandatory to have 505b(2) application bio-equivalent to current reference listed drug?"

regards,

Mithu
 
dshah
★★  

India/United Kingdom,
2023-05-05 15:38
(211 d 01:18 ago)

@ Mithu
Posting: # 23545
Views: 904
 

 505 b(2) application & requirement of bioequivalence

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Hello Mithu!

As we rely on existing PKPD relationship, toxicity data and other pharmacology data of reference drug, the BE is required.

Regards,
Divyen
 
Mithu
★    

India,
2023-05-11 09:58
(205 d 06:59 ago)

@ dshah
Posting: # 23548
Views: 827
 

 505 b(2) application & requirement of bioequivalence

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Hi Divyen,

Thank you for your reply.

regards,

Mithu
 
Achievwin
★    

US,
2023-05-05 18:08
(210 d 22:49 ago)

@ Mithu
Posting: # 23546
Views: 938
 

 505 b(2) application & requirement of bio­equi­va­lence

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Hello Mithu:

505 (b)(2) is all about the submission and marketing strategy. Most of the 505(b)(2) applications take BE route as drug Chemistry, safety and efficacy along with biopharmaceutics is already known and BE is used as a knowledge (claim) gap bridging approach. There are other means you can get 505(b)(2. Please review different guidance (FDA, EMA etc.) or white papers on 505(b)(2).

Hope this helps
 
Mithu
★    

India,
2023-05-11 09:58
(205 d 06:58 ago)

@ Achievwin
Posting: # 23549
Views: 810
 

 505 b(2) application & requirement of bio­equi­va­lence

Post reply
Hello Achievwin,

Thank you for your reply.

regards,

Mithu
 
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