|
|
|
|
|
by nradov
1156 days ago
|
|
Drug discovery is the easy part. Many of the molecules come out of publicly funded academic research. The hard, expensive part is running the large-scale human trials necessary to demonstrate the level of safety and efficacy needed for FDA approval. There is no way to do that cheaply. That's why patents are needed as an economic incentive. In theory the government could nationalize the entire pharmaceutical industry but there is no evidence that bureaucrats are capable of reliably picking the right candidate drugs. Countries with weak IP protections do relatively little new drug development. |
|
I'm not convinced that the govt bureaucrats would do a worse job than drug co bureaucrats. Current studies are poorly designed, implemented incorrectly, results are cherry-picked and gamed, p-hacking lives, ... This is an industry that can't even seem to accept pre-registration.
Also, as you say, most of these molecules come from publicly funded research. Why would the group funding the first set of research (and producing more molecules than industry) automatically be bad at the second?
In all, I'm not convinced that "Drug discovery is the easy part." If it was so easy, then why don't drug co's do it, and save the licensing fees?