Loky do
★    

Egypt,
2024-03-04 11:27
(833 d 06:42 ago)

Posting: # 23892
Views: 6,501
 

 multiple dose studies [Design Issues]

Dears

I have a solifenacin succinate/tamsulosin HCl bioequivalence study, I will perform a multiple-dose study for tamsulosin modified release for Europe, I'm a little confused about the planned washout for this study as there are no enough public assessment reports for the combination, should I take in account the solifenacin washout period also or to design on tamsulosin only is enough (i.e one-week washout between 2 periods from last dose)

thanks in advance


Edit: Category changed; see also this post #1[Helmut]
dshah
★★  

India,
2024-03-08 18:36
(828 d 23:33 ago)

@ Loky do
Posting: # 23895
Views: 5,102
 

 multiple dose studies

Hello Loky do!


❝ I have a solifenacin succinate/tamsulosin HCl bioequivalence study, I will perform a multiple-dose study for tamsulosin modified release for Europe, I'm a little confused about the planned washout for this study as there are no enough public assessment reports for the combination, should I take in account the solifenacin washout period also or to design on tamsulosin only is enough (i.e one-week washout between 2 periods from last dose)


As this is FDC- both the drug needs to be analyzed and thus also consider Solifenacin for washout consideration.

Regards,
Divyen
Loky do
★    

Egypt,
2024-03-11 12:20
(826 d 05:49 ago)

@ dshah
Posting: # 23900
Views: 5,141
 

 multiple dose studies

❝ As this is FDC- both the drug needs to be analyzed and thus also consider Solifenacin for washout consideration.

I'm a little confused :confused: why to analyze solifenacin as it is immediate release and the concern towards tamsulosin as it is the delayed release one, even if I took into consideration the washout of both, are the results of solifenacin, in this case, affect those of tamsulosin?

Regards,
Loky


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]
dshah
★★  

India,
2024-03-12 18:37
(824 d 23:32 ago)

@ Loky do
Posting: # 23905
Views: 5,025
 

 multiple dose studies

Hello Loky do!

❝ I'm a little confused :confused: why to analyze solifenacin as it is immediate release and the concern towards tamsulosin as it is the delayed release one, even if I took into consideration the washout of both, are the results of solifenacin, in this case, affect those of tamsulosin?


Kindly refer section 3 of EMA guideline on FDC.
[image]

Considering as a sponsor, the analysis of solifenacin adds a cost. But as a regulator- if you are taking the sample- why it is not analyzed? Any SE relation with PK would not be feasible, then.

Regards,
Divyen
UA Flag
Activity
 Admin contact
23,654 posts in 4,992 threads, 1,570 registered users;
112 visitors (0 registered, 112 guests [including 10 identified bots]).
Forum time: 19:09 CEST (Europe/Vienna)

The idea is to try and give all the information to help others
to judge the value of your contribution;
not just the information that leads to judgment
in one particular direction or another.    Richard Feynman

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