AI Drugs Head to the Clinic: Isomorphic Labs Prepares Human Trials

Isomorphic Labs, an Alphabet subsidiary and spin-off of the DeepMind lab, is preparing to shake up the pharmaceutical industry. At the WIRED Health conference in London, company president Max Jaderberg announced that its first drugs, designed entirely by artificial intelligence, are moving into human clinical trials. For years, neural networks only predicted protein structures. Now the algorithms are creating real molecules to treat complex diseases. If the trials succeed, the years-long drug development process could shrink dramatically, by a factor of dozens, opening the way to faster and cheaper treatment of previously incurable diseases.

AI-processed from Wired; edited by Hamidun News
AI Drugs Head to the Clinic: Isomorphic Labs Prepares Human Trials
Source: Wired. Collage: Hamidun News.
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For years, the pharmaceutical industry has lived on promises that artificial intelligence was about to change the rules of the game and radically shorten a molecule's path from the lab to the pharmacy shelf. Now those abstract promises are taking physical form. At the WIRED Health conference in London, Isomorphic Labs president Max Jaderberg made a statement that could split the history of modern medicine into "before" and "after."

The Alphabet subsidiary, which grew out of the legendary DeepMind research lab, is officially preparing to move a whole line of neural-network-designed drugs into human clinical trials. These are no longer theoretical calculations or pretty three-dimensional models on data center screens, but real chemical compounds ready to face the toughest proving ground there is: the human body.

To grasp the true scale of this event, it helps to go back to the origins of Isomorphic Labs. The ambitious project rests on the monumental scientific success of AlphaFold, the system that a few years ago solved the half-century-old protein folding prediction problem. By decoding the three-dimensional structures of practically all proteins known to science, researchers obtained a detailed map of life's building blocks.

But a map is not a drug. Isomorphic Labs was spun out as a separate company precisely to turn this unprecedented biological data into commercial therapeutics. Jaderberg's statement confirms that the move from purely fundamental science to applied molecular engineering has succeeded, and that the company has already built a broad, promising portfolio of new medicines.

Traditional drug development is an extremely inefficient and exhausting marathon that lasts ten to fifteen years on average and costs pharmaceutical corporations billions of dollars. Most of that time and astronomical budget goes to blind trial and error: scientists test millions of existing chemical compounds hoping to find the one that binds to the right target without killing the patient through toxicity. Isomorphic Labs' approach radically changes this outdated paradigm. Instead of looking for a needle in an endless haystack, its AI algorithms work as molecular architects. They design molecules from scratch to fit a specific protein, while simultaneously predicting their side effects, solubility and ability to cross the body's difficult biological barriers.

Yet the move to human clinical trials is an uncompromising moment of truth that carries enormous risks. However sophisticated machine learning algorithms may be, computational biology still faces the phenomenal unpredictability of living systems. What works flawlessly in silico (in a computer simulation) and shows excellent results in vitro (in a laboratory test tube) can behave completely unexpectedly in the bloodstream of a living person because of cascading biological reactions.

That is why the entire healthcare industry will watch the first phases of these trials with particular attention. Success for Isomorphic Labs would be irrefutable proof that generative AI can do more than generate coherent text or photorealistic images: it can design safe, effective physical objects that save human lives.

The consequences of successfully completing these trials would reach far beyond a single company and shake the foundations of the global healthcare system. The biggest players in the traditional market, which are already beginning to sign multimillion-dollar contracts with computational biology startups, will have to completely rebuild their R&D centers. We will see tech giants finally erase the line between Silicon Valley and classic Big Pharma. The ability of algorithms to design drugs quickly means humanity could respond to new viral threats in the shortest possible time, and could also create targeted therapies for rare genetic diseases, which corporations previously considered economically unviable because of the small number of patients.

The announcement made on the WIRED Health stage marks the start of a completely new era in science: the era of programmable pharmacology. If Isomorphic Labs' drugs prove absolutely safe and therapeutically effective in human trials, we will finally move from the historical age of chance discoveries to an age of deliberate engineering of human health. Artificial intelligence stops being merely a powerful analytical tool for scientists; it becomes a full-fledged creator of new medical solutions, rapidly bringing closer the day when developing a life-saving drug for a new disease takes a matter of months, not long decades.

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Zhemal Khamidun — CPO at Alpina Digital, product manager of AlpinaGPT. Building AI products since 2019. Hamidun News is a pet project that grew into a production aggregator with 6,000+ readers.
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