← Back to Library

Americans should celebrate China's biotech revolution

Richard Hanania flips the script on a dominant geopolitical narrative: instead of fearing China's biotech surge as an existential threat, he argues we should celebrate it as a global health victory. While Washington fixates on containment and "decoupling," this piece offers a startling counter-perspective grounded in the mechanics of drug development itself, suggesting that American anxiety is actively harming patients by stifling the very partnerships that accelerate cures.

The Mechanics of Speed

Hanania begins by dismantling the assumption that American regulatory rigor equals superior safety. He points to a stark reality: China has become a global leader in biotech not through magic, but through deliberate industrial policy and streamlined bureaucracy. "China's ongoing biotechnology transformation is the product of deliberate industrial policy," Hanania writes, highlighting how initiatives like Made in China 2025 explicitly targeted medical technologies as strategic priorities.

Americans should celebrate China's biotech revolution

The author zeroes in on the clinical trial ecosystem as the true differentiator. In the U.S., a new drug often hits a wall of red tape before it ever touches a patient. Hanania notes that the process involves an "Investigational New Drug application," a document that can run to thousands of pages and is laden with requirements unnecessary at early stages. By contrast, China's system allows trials to launch in roughly six months. This speed isn't just administrative; it's scientific. "The most valuable thing early-stage trials enable is iteration," he argues. These rapid cycles allow for tight feedback between the clinic and the lab, a crucial advantage when engineering complex therapies like CAR-T cells where animal models fail to replicate human tumor geometry.

Critics might argue that speed comes at the cost of safety or data integrity. However, Hanania counters this by pointing out that private sector investors are not naive; if Chinese data were fundamentally untrustworthy on a mass scale, capital would have fled long ago. He notes that recent reforms in China have actually improved quality and alignment with international standards, suggesting the U.S. is lagging behind in efficiency rather than leading in safety.

"Talent acquisition plus the removal of burdensome regulations that don't pass a cost-benefit test."

The Zero-Sum Trap

The piece takes a sharp turn to critique the prevailing political mindset in Washington, which views biotech through a zero-sum lens. Hanania observes that while the fear of losing the "race" can spur domestic reform, it often leads to self-sabotaging policies designed to hurt China rather than help America. He cites Congressman John Moolenaar's push to restrict U.S.-China cooperation and limit licensing deals as a prime example of this paranoia.

Hanania challenges the ethical arguments used by protectionists, specifically claims about involuntary trial participation in China. "Yeah, I'd like to see data or actual evidence on the involuntary part," he writes, dismissing these allegations as unproven exaggerations used to deny legitimate progress. He further argues that the American conception of medical ethics often hinders research into curing disease by protecting privacy preferences that patients themselves might not prioritize in a life-or-death scenario.

The author reframes the potential risks of Chinese dominance. Unlike nuclear weapons or advanced AI, where one nation's gain could be another's strategic loss, biotech is "almost purely positive sum." If China cures cancer, they will sell it to us. Even if they tried to hoard a breakthrough, the mere existence of the cure provides proof of concept that American companies can follow. "Perhaps China can cut us off from a vital drug in the middle of a war or other emergency, but this is about manufacturing rather than development," Hanania asserts, distinguishing between the knowledge frontier and the supply chain.

"Preventing a US-China partnership that cures cancer seems like a pretty disastrous outcome."

Knowledge as a Public Good

Hanania's most provocative claim centers on intellectual property (IP). He acknowledges that Chinese firms often replicate American work at lower costs, but he challenges the notion that this is purely negative for Americans. "Someone involved in the industry testified 'that for every innovative U.S. biotechnology firm, there is a 'shadow' Chinese firm working to replicate its work at a lower cost,'" Hanania quotes. He argues that while this hurts specific corporations, it benefits consumers by revealing how to create drugs more cheaply.

He posits that knowledge of cheaper production methods is a public good, similar to fundamental scientific discoveries. "All of this is to say that IP theft is probably at most a small problem, and might actually be good on balance, even from an American perspective," he concludes. This perspective shifts the focus from protecting market share to maximizing human health outcomes globally.

The author also touches on the historical context of engagement, noting that while the hope that trade would democratize China failed, the economic benefits of a billion-plus people innovating and getting wealthier remain valid regardless of their political system. "A billion-plus people innovating and getting wealthier has positive effects on the rest of the world regardless of what kind of political system they live under," he writes, urging policymakers to prioritize friendly commerce over antagonism.

Bottom Line

Hanania's argument is a powerful corrective to the fear-driven rhetoric dominating Washington, successfully reframing biotech as a field where cooperation yields universal health benefits rather than strategic losses. Its greatest vulnerability lies in its optimistic assumption that supply chains will always be reversible and that IP theft never truly stifles long-term innovation incentives. Readers should watch whether this nuanced view can survive the political pressure of a "race" narrative that thrives on simple, fear-based mobilization.

Deep Dives

Explore these related deep dives:

  • Investigational New Drug

    The article contrasts the US regulatory bottleneck with China's speed, and this specific FDA document represents the multi-year, thousands-of-page hurdle that delays early-stage iteration in American oncology.

  • Thousand Talents Plan

    While the text mentions this policy as a driver for returning scientists, its Wikipedia entry details the specific mechanisms and controversies of how China systematically reverse-engineered Western biotech expertise to build domestic industry leaders like BeiGene.

  • Clinical trial

    The author credits this specific clinical model as China's structural advantage, and understanding its Wikipedia definition reveals how it bypasses traditional sponsor-led bureaucracy to allow oncologists to rapidly test hypotheses directly in patients.

Sources

Americans should celebrate China's biotech revolution

by Richard Hanania · · Read full article

Note: To do book promotional stuff, I’ll be in DC Monday and Tuesday this week, and NYC for about a week starting Wednesday. I may do one or two meetups. To remain informed, check the X feed and Substack notes, where I’ll post updates on what I’m doing.

Ruxandra Teslo and Amol Punjabi recently wrote about how a Chinese startup developed a new drug that significantly extends the lifespans of people with multiple myeloma.

This is part of a larger story in which China has suddenly become a global leader in biotech over the last decade. Here’s a figure from an Economist report on the topic last year.

A figure in the December 2025 report of the congressional National Security Commission on Emerging Biotechnology (NSCEB) helpfully shows how drug development works and the rise of China in this area.

Teslo and Punjabi point out that the government has done this by enacting the kind of reforms that smarter critics of the FDA have been advocating for years.

China’s ongoing biotechnology transformation is the product of deliberate industrial policy. The Made in China 2025 initiative explicitly identified biotechnology and advanced medical technologies as strategic national priorities, and a series of targeted policies followed. Among them was the Thousand Talents Plan, designed to draw overseas Chinese scientists back from Western institutions. BeiGene, Innovent, and Junshi, which are now three of China’s leading oncology biotechs, were all founded or are now led by researchers who had trained in the United States before returning home.

Yet perhaps the most consequential advantage China has built lies in its clinical trial ecosystem. Chinese hospitals make extensive use of investigator-initiated trials. These are early-stage studies that allow oncologists to quickly assess whether a drug shows genuine promise. In China, such a trial can be up and running within roughly six months of a patient consultation with an academic oncologist. In the United States, the same process can take eighteen months or more, bogged down by regulatory preparation that includes a lengthy Investigational New Drug application. This is a document that can run to thousands of pages and is laden with a host of requirements which are unnecessary at such an early stage of development.

The most valuable thing early-stage trials enable is iteration. They allow tight feedback between the clinic and the lab. There are countless ways to engineer a better CAR-T cell, and many cannot be ...