Farmacevt
☆    

North Macedonia,
2022-01-18 17:01
(825 d 20:22 ago)

Posting: # 22732
Views: 1,684
 

 ODT in BE study [Design Issues]

Dears,

I would appreciate if you can share your opinion regarding this particular case:

IF you develop generic orodispersible tablet (ODT) and the reference formulation is immediate release tablet (obviously it can be administrate only with water) is it enough to perform two way cross-over study where the ODT will be administrated without water and the reference tbl. with water, or 3 arm study (ODT administrated in both ways with and without water and the reference with water) should be performed?


Thank you
dshah
★★  

India/United Kingdom,
2022-01-18 20:08
(825 d 17:15 ago)

@ Farmacevt
Posting: # 22733
Views: 1,362
 

 ODT in BE study

Dear Farmacevt!
It is advisable to perform 3 way BE study i.e.- with and without water for ODT and Reference with water. This will also have advantage to prove that there is no significant difference in PK for ODT when administered with and without water.
Regards,
Dshah
UA Flag
Activity
 Admin contact
22,990 posts in 4,826 threads, 1,646 registered users;
62 visitors (1 registered, 61 guests [including 4 identified bots]).
Forum time: 14:23 CEST (Europe/Vienna)

If you don’t like something change it;
if you can’t change it, change the way you think about it.    Mary Engelbreit

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5