Science has long been humanity’s greatest catalyst for progress. Yet, mention “science” today and you’re likely to be met with scepticism. When headlines proclaim “Science says…” they’re more likely to elicit eye rolls than genuine interest. This growing disillusionment isn’t without cause—science has increasingly become a marketing buzzword, diluted by corporate interests and divorced from its fundamental purpose: advancing human knowledge and well-being.
Decentralised Science is a new paradigm that promises to rebuild scientific research on stronger foundations. The current spotlight of DeSci projects focuses on pharmaceutical drugs, one of the low-hanging fruits for improving the most important resource for humanity - our health.
Traditional science funding is broken. Academic researchers spend up to 40% of their time writing grant proposals, with success rates below 20%. As Federal funding dipped, private funding increased but is heavily concentrated in the hands of big businesses.
The pharmaceutical industry has evolved into a high-stakes game where the odds are stacked against innovation. Consider this: for every 10,000 compounds discovered, only 1 makes it to market. The journey is brutal. Only 10% of drugs that enter clinical trials ever receive FDA approval, with the process taking upto 15 years and costing over $2.6 billion per successful drug.
In the 1990s, Pharma’s centralisation seemed like a boon—it brought efficiency, streamlined supply chains, and enabled the rapid scaling of drug discoveries. But what started as a well-oiled machine for innovation has devolved into a bottleneck, with the same players guarding their monopolies at the expense of progress and ballooning costs.
In the current model, a biotech startup spends years seeking NIH funding for early-stage discovery and then raises a $15M Series A to move into preclinical trials. If successful, it licenses the IP to a Big Pharma company which invests $1B+ to take it through clinical trials and commercialisation.
Here’s where incentives get twisted. Instead of focusing on groundbreaking new treatments, Big Pharma has mastered a more profitable game: patent manipulation. The playbook is simple. When a lucrative drug patent nears expiration, file dozens of secondary patents on minor modifications— new delivery methods, slightly altered formulations, or even just new uses for the same drug.
Take the case of Humira, an anti-inflammatory drug by AbbVie. Humira has been one of the best-selling drugs in the world for years, raking in over $20 billion annually. Its original patent expired in 2016, but AbbVie filed more than 100 additional patents to block generic competition. This legal manoeuvring delayed affordable alternatives from entering the market, costing patients and healthcare systems billions.
In the recent Desci debate between @tarunchitra and @benjileibo, this stalling of pharma innovation was brought up with the observation of Eroom’s law. (Reverse of Moore’s law)
These practices are symptomatic of a larger issue: the capture of innovation by profit motives. Pharmaceutical companies funnel resources into tweaking existing drugs—making slight chemical modifications or finding new delivery mechanisms—not because they offer major health benefits but because they can secure fresh patents and extend profitability.
At the same time, the global research community, brimming with talent and creativity, remains locked out of this process. Young researchers are shackled by limited grant funding, bureaucratic red tape, and a publish-or-perish culture that priorities headline-worthy topics over meaningful but less glamorous work. As a result, rare diseases, neglected tropical diseases, and early-stage exploratory research are woefully underfunded.
DeSci is fundamentally a coordination mechanism. It aggregates human capital—biologists, chemists, researchers—across the globe, enabling them to synthesise, test, and iterate without reliance on traditional institutions. Funding, too, is reimagined. Instead of government grants or corporate sponsorships, decentralised autonomous organizations (DAOs) and tokenised incentives democratise access to capital.
The traditional pharmaceutical supply chain is a rigid, siloed process dominated by a handful of gatekeepers. It typically follows a linear path: centralised data generation, discovery in isolated labs, high-cost trials, exclusive manufacturing, and restricted distribution. Each step is optimized for profitability, not accessibility or collaboration.
In contrast, DeSci introduces an open and collaborative chain that reimagines each stage, democratising participation and accelerating innovation. Here’s how they compare:
Results of these trials are recorded and streamed on Pump.science
BioDAOs hold over $33M in IPT tokenized through Molecule’s framework
DAOs struggle with coordinating complex tasks and maintaining accountability - very few DAOs have demonstrated sustainable success in managing long-term projects. DeSci faces an even greater challenge: it needs researchers to coordinate on complex problems, meet research deadlines, and maintain scientific rigour, all without traditional institutional oversight.
Traditional science, for all its flaws, has established mechanisms for peer review and quality control. DeSci must either adapt these systems or develop entirely new accountability frameworks. This challenge is particularly acute given the high stakes involved in medical research. A failed NFT project loses money, but a poorly executed medical trial could cost lives.
Critics argue that DeSci is merely speculative—little more than a trading game. They’re not entirely wrong. History shows that new technologies often struggle until a breakthrough success captures the public imagination. Much like how AI agents gained mainstream attention through agents like @aixbt_agent, DeSci likely needs a defining moment to shift perceptions.
The future might not look exactly as DeSci proponents envision. Perhaps it’s not about replacing traditional institutions entirely, but creating parallel systems that force innovation through competition. Or maybe it’s about finding specific niches—like rare disease research—where traditional models have failed.
Imagine a world where brilliant minds tackle humanity’s greatest medical challenges unrestricted by borders or budgets—where a breakthrough in a Chinese lab can be instantly verified in Singapore and scaled in São Paulo.
Pioneers are building towards this future, one experiment at a time. Take @bryan_johnson—an independent biohacker experimenting with off-label drugs and unorthodox therapies. While his methods might alarm traditionalists, he represents the ethos of DeSci: experimentation over gatekeeping.
Science has long been humanity’s greatest catalyst for progress. Yet, mention “science” today and you’re likely to be met with scepticism. When headlines proclaim “Science says…” they’re more likely to elicit eye rolls than genuine interest. This growing disillusionment isn’t without cause—science has increasingly become a marketing buzzword, diluted by corporate interests and divorced from its fundamental purpose: advancing human knowledge and well-being.
Decentralised Science is a new paradigm that promises to rebuild scientific research on stronger foundations. The current spotlight of DeSci projects focuses on pharmaceutical drugs, one of the low-hanging fruits for improving the most important resource for humanity - our health.
Traditional science funding is broken. Academic researchers spend up to 40% of their time writing grant proposals, with success rates below 20%. As Federal funding dipped, private funding increased but is heavily concentrated in the hands of big businesses.
The pharmaceutical industry has evolved into a high-stakes game where the odds are stacked against innovation. Consider this: for every 10,000 compounds discovered, only 1 makes it to market. The journey is brutal. Only 10% of drugs that enter clinical trials ever receive FDA approval, with the process taking upto 15 years and costing over $2.6 billion per successful drug.
In the 1990s, Pharma’s centralisation seemed like a boon—it brought efficiency, streamlined supply chains, and enabled the rapid scaling of drug discoveries. But what started as a well-oiled machine for innovation has devolved into a bottleneck, with the same players guarding their monopolies at the expense of progress and ballooning costs.
In the current model, a biotech startup spends years seeking NIH funding for early-stage discovery and then raises a $15M Series A to move into preclinical trials. If successful, it licenses the IP to a Big Pharma company which invests $1B+ to take it through clinical trials and commercialisation.
Here’s where incentives get twisted. Instead of focusing on groundbreaking new treatments, Big Pharma has mastered a more profitable game: patent manipulation. The playbook is simple. When a lucrative drug patent nears expiration, file dozens of secondary patents on minor modifications— new delivery methods, slightly altered formulations, or even just new uses for the same drug.
Take the case of Humira, an anti-inflammatory drug by AbbVie. Humira has been one of the best-selling drugs in the world for years, raking in over $20 billion annually. Its original patent expired in 2016, but AbbVie filed more than 100 additional patents to block generic competition. This legal manoeuvring delayed affordable alternatives from entering the market, costing patients and healthcare systems billions.
In the recent Desci debate between @tarunchitra and @benjileibo, this stalling of pharma innovation was brought up with the observation of Eroom’s law. (Reverse of Moore’s law)
These practices are symptomatic of a larger issue: the capture of innovation by profit motives. Pharmaceutical companies funnel resources into tweaking existing drugs—making slight chemical modifications or finding new delivery mechanisms—not because they offer major health benefits but because they can secure fresh patents and extend profitability.
At the same time, the global research community, brimming with talent and creativity, remains locked out of this process. Young researchers are shackled by limited grant funding, bureaucratic red tape, and a publish-or-perish culture that priorities headline-worthy topics over meaningful but less glamorous work. As a result, rare diseases, neglected tropical diseases, and early-stage exploratory research are woefully underfunded.
DeSci is fundamentally a coordination mechanism. It aggregates human capital—biologists, chemists, researchers—across the globe, enabling them to synthesise, test, and iterate without reliance on traditional institutions. Funding, too, is reimagined. Instead of government grants or corporate sponsorships, decentralised autonomous organizations (DAOs) and tokenised incentives democratise access to capital.
The traditional pharmaceutical supply chain is a rigid, siloed process dominated by a handful of gatekeepers. It typically follows a linear path: centralised data generation, discovery in isolated labs, high-cost trials, exclusive manufacturing, and restricted distribution. Each step is optimized for profitability, not accessibility or collaboration.
In contrast, DeSci introduces an open and collaborative chain that reimagines each stage, democratising participation and accelerating innovation. Here’s how they compare:
Results of these trials are recorded and streamed on Pump.science
BioDAOs hold over $33M in IPT tokenized through Molecule’s framework
DAOs struggle with coordinating complex tasks and maintaining accountability - very few DAOs have demonstrated sustainable success in managing long-term projects. DeSci faces an even greater challenge: it needs researchers to coordinate on complex problems, meet research deadlines, and maintain scientific rigour, all without traditional institutional oversight.
Traditional science, for all its flaws, has established mechanisms for peer review and quality control. DeSci must either adapt these systems or develop entirely new accountability frameworks. This challenge is particularly acute given the high stakes involved in medical research. A failed NFT project loses money, but a poorly executed medical trial could cost lives.
Critics argue that DeSci is merely speculative—little more than a trading game. They’re not entirely wrong. History shows that new technologies often struggle until a breakthrough success captures the public imagination. Much like how AI agents gained mainstream attention through agents like @aixbt_agent, DeSci likely needs a defining moment to shift perceptions.
The future might not look exactly as DeSci proponents envision. Perhaps it’s not about replacing traditional institutions entirely, but creating parallel systems that force innovation through competition. Or maybe it’s about finding specific niches—like rare disease research—where traditional models have failed.
Imagine a world where brilliant minds tackle humanity’s greatest medical challenges unrestricted by borders or budgets—where a breakthrough in a Chinese lab can be instantly verified in Singapore and scaled in São Paulo.
Pioneers are building towards this future, one experiment at a time. Take @bryan_johnson—an independent biohacker experimenting with off-label drugs and unorthodox therapies. While his methods might alarm traditionalists, he represents the ethos of DeSci: experimentation over gatekeeping.