Loky do ★ Egypt, 2024-03-04 11:27 (434 d 04:36 ago) Posting: # 23892 Views: 3,720 |
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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 (429 d 21:27 ago) @ Loky do Posting: # 23895 Views: 2,812 |
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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) ❝ Regards, Divyen |
Loky do ★ Egypt, 2024-03-11 12:20 (427 d 03:44 ago) @ dshah Posting: # 23900 Views: 2,821 |
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❝ As this is FDC- both the drug needs to be analyzed and thus also consider Solifenacin for washout consideration. ![]() 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 (425 d 21:27 ago) @ Loky do Posting: # 23905 Views: 2,713 |
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Hello Loky do! ❝ I'm a little confused ❝ ![]() 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 |