(136 d 21:03 ago)
Posting: # 23560
the so-called ‘Citizen Petitions’ make the lawyers of innovators richer. Here is a recent one calling the FDA’s approval of an ANDA based on a study in Indian males ‘unlawful’…
Dif-tor heh smusma 🖖🏼 Довге життя Україна!
The quality of responses received is directly proportional to the quality of the question asked. 🚮
(135 d 20:57 ago)
Posting: # 23562
MSN’s findings also diverge substantially from the Cmax and AUC∞ found for the same lot of reference listed drug that was tested by another generic manufacturer (Apotex) with an approved ANDA for tasimelteon (No. 211607).
So they acknowleged another generic, but don't have any problems with that. Why? Take a look at this FDA letter to Apotex:
Therefore, final approval cannot be granted until:
regarding current study from your link:
Exhibit 2, 2015 Guidance, supra. Accordingly, under FDA’s guidance, MSN’sstudy should have included females and males, as well as individuals from a range of races and ethnicities, reflective of the overall U.S. population. See Roth Decl. ¶¶ 41-42. Because MSN’s study did not, FDA unlawfully concluded that “the demographics profile of subjects completing the bioequivalence study [is] in agreement with the current drug product recommendation.” Exhibit 1, MSN Bioequivalence Review, supra, at 23; see also Roth Decl. ¶¶ 47-59.
Didn't we see something similar already in 2000s?