Comment by notahacker
7 hours ago
Yeah. It's possible to think that there are cases where lowering the cost of first phase trials or making it relatively simple for people capable of offering informed consent to obtain access to existing safe medications currently undergoing trials for their specific ailments and thinking that a person who claims to have "designed an RNA vaccine" by asking an LLM to teach him about RNA and now wants to inject it into animals under his care might be the exact thing such laws were meant to restrict.
Plus as others have pointed out, LLMs are much better at generating something that looks like compliance documentation than they are at designing drugs (and providing generic background info on compliance processes than they are at relatively little-documented cutting edge research), so if most people aren't instantly sceptical of a yarn spun about how a layman with ChatGPT easily taught himself enough to find an RNA immunotherapy cure for his dog but then was stymied by the amount of typing involved in a 100 page document, it's a good indication of why barriers to even nominally consenting people trying experimental stuff exist.
The LLM did not design the drug. The LLM summarized some papers on how to design similar drugs, and then a dozen specialized tools were used in an established pipeline to design the drug. You people need to read the article and read the background before writing nonsense based on your assumptions.
Here's a previous comment of mine talking about personalized mRNA vaccines with useful citations: https://news.ycombinator.com/item?id=47210284
Funny how you keep skipping the unbelievable part of the story out of your replies: why would he spend 3 month hand typing a document that an LLM can definitely make at least 80% of it in one shot?
Have you ever tried writing a long, complicated document with an LLM? The last 20% takes 99% of the work.
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