4 ms·
The initial patent for semaglutide specifically was issued in 2008 and is under protection for 20 years -- while liraglutide has been around for much longer, se
by andrewla 2y ago
The initial patent for semaglutide specifically was issued in 2008 and is under protection for 20 years -- while liraglutide has been around for much longer, semaglutide is relatively new in patent terms.
So presumably the licensed DMF facilities are operating under a license from Novo Nordisk, because otherwise they'd be shut down. But why do the terms of the license allow them to sell to anyone else?
You are correct that the use specifically for weight loss is newer and the FDA's labyrinthine procedures give Novo Nordisk exclusivity for a significant amount of time after that.
- simoncion 2y ago> In the end this comes down to a Reddit post from Henry's, one of the online compounding pharmacies I disagree. Alexander mentions several other compounding pharmacies that will sell you the same medication if you present a subscription, so it's not just one place that's selling this stuff: > HenryMeds is $297/month, Eden is $296, Mochi is $254... You probably do not know this, but the fellow has been a psychiatrist for a decade or more. He's also aware of the business and regulatory side of the medical profession, so I expect the assertion that "But the law says that compounding pharmacies are allowed to step in and compete with Big Pharma during a shortage." is true and accurate. The Reddit post claims a source for the chemicals, but the explanation about what compounding pharmacies are doing during times of medication supply shortage and how they can legally do it come from industry knowledge. > But why do the terms of the license allow them to sell to anyone else? Likely because the FDA permits compounding pharmacies to sell Big Pharma drugs when there's a shortage of them. If compounding pharmacies can get reliable access to the same chemicals that Big Pharma is selling, then the bottleneck is somewhere in Big Pharma's side of the machine (rather than the chemical "feedstock" production side), and the FDA has a strong interest in permitting entities that can take up the slack to do so. I can't imagine the FDA has any interest at all in undermining its ability to solve drug shortages by enlisting secondary drug manufacturers, so I expect any "feedstock" production agreements must not restrict the ability for the "feedstock" producer to sell to secondary drug manufacturers when the FDA deems it necessary to permit them to sell products from that "feedstock".