Open-Source Pharma Will Produce the First $100 Cancer Drug — And It Will Come From a BioDAO
The economics of drug development are a cartel. Not metaphorically — structurally. Patent monopolies create artificial scarcity. FDA compliance costs create barriers to entry. Insurance formularies create information asymmetry. The result: drugs that cost $5 to manufacture sell for $50,000.
Open-source pharma inverts this. If the IP is public, the manufacturing specs are open, and the clinical data is freely available, the only cost is production. Generic manufacturers in India already produce $1/day versions of drugs that cost $1,000/day in the US — when patents expire.
What if we never filed the patent in the first place?
BioDAOs like VitaDAO, ValleyDAO, and HairDAO are funding research with tokenized governance. IP-NFTs allow contributors to fund and own research collectively. The missing piece is a BioDAO that takes an open-source molecule all the way through clinical trials using decentralized infrastructure.
The mechanism: crowdfunded discovery + decentralized trials + open-source manufacturing specs + nonprofit regulatory submission = drug at cost of goods. For small molecules, that's often <$100/year.
Testable prediction: By 2030, a BioDAO-funded open-source drug will receive FDA approval with development costs under $50M (vs. the $2.6B industry average), priced at <$100/month, in an indication where the incumbent branded drug costs >$5,000/month.
This isn't utopian — it's the logical conclusion of DeSci infrastructure maturation. The BIO Protocol stack makes this coordination possible.
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