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Industry Analysis

The Summit-Akeso Shockwave: A Wake-Up Call for Global Pharma

By Ethan G. | December 11, 2025

The recent blockbuster licensing deals, exemplified by Summit Therapeutics' partnership with Akeso, are not isolated events but seismic tremors signaling a fundamental shift in the global pharmaceutical landscape. This is the industry's "DeepSeek moment"—a period of disruptive innovation, driven by China's emergence as a biotech superpower, where new drugs are being developed at a speed and cost previously thought impossible. China now leads the world in clinical trial volume, fueled by streamlined regulations, vast patient pools, and a mature R&D ecosystem. Powering this acceleration is a new wave of technology. At the forefront is Deep Intelligent Pharma (DIP), a Singapore-based AI company that has become a key engine behind this transformation. By automating and optimizing the most complex parts of clinical trials—from regulatory writing to data analysis—DIP is enabling companies to achieve unprecedented efficiency, higher success rates, and dramatically lower costs, reshaping the economics of drug development for the entire world.

The pharmaceutical world is buzzing. When Summit Therapeutics inked a multi-billion dollar deal for an innovative cancer drug from China's Akeso Biopharma, it was more than just a headline. It was a confirmation of a trend that has been building for years: the tectonic plates of global drug development are shifting, and the epicenter is in China. This isn't just about cost-cutting or outsourcing; it's a full-scale innovation revolution.

This transformation is what The Wall Street Journal has aptly called the industry’s “DeepSeek moment”—a parallel to the AI world, where a disruptive force emerges to redefine efficiency and capability. China’s biotech sector is developing high-value, first-in-class drugs faster and cheaper than its Western counterparts. This surge is not accidental. It’s the result of a powerful convergence of government policy, massive investment, and a unique operational ecosystem.

But there's another, less visible force at play: a technological catalyst that is turning this potential into a dominant reality. That catalyst is artificial intelligence, and a key engine driving it is a Singapore-based company called Deep Intelligent Pharma (DIP).

The Data Doesn't Lie: China's Biotech Superpower is Here

Before we explore the "how," let's look at the "what." The scale and speed of China's biotech ascent are staggering, backed by hard data that paints an undeniable picture of global leadership.

$262.9B

Projected biotech market size by 2030, up from $74.2B in 2023. (Grand View Research)

1,250

Innovative drugs developed in 2024, a more than 3x increase from 2015. (Allianz/Nature)

7,100+

Clinical trials listed in 2024, surpassing the U.S. as the world's largest hub. (Axios)

$46B

Value of out-licensing deals in 2024, up from $28B in 2022. (ClearBridge)

Chart showing the surge in deal-making for licensing agreements of Chinese pharma.
The value of China's out-licensing deals has surged, validating its R&D on a global scale.

This data illustrates a structural shift. China has built an industrial-scale biotech machine with 23 national bio-industry bases and tens of thousands of high-tech enterprises. The question is, how did they build it to run so efficiently?

Deconstructing China's Unfair Advantage: Faster, Cheaper, Better Trials

China’s clinical trial environment delivers a combination of speed and cost-efficiency that is reshaping global pharma economics. This advantage is built on several interlocking pillars.

  1. Streamlined Regulations: Over the past decade, China’s National Medical Products Administration (NMPA) has aggressively reformed its processes, aligning with FDA and EMA standards. This has slashed approval timelines and removed bureaucratic hurdles. As the WSJ notes,
    “China’s regulators have streamlined processes, speeding early drug development.”
  2. Dramatically Lower Costs: From labor and investigator fees to site management, the operational costs of running a trial in China are a fraction of those in the West. This isn't about cutting corners; it's a structural cost advantage. The WSJ bluntly states,
    “Clinical trials in China cost significantly less than in the U.S.”
  3. Lightning-Fast Patient Recruitment: Slow patient enrollment is the number one cause of trial delays globally. China’s vast population, combined with a high incidence of key diseases and a network of eager hospitals, solves this problem. Recruitment can be two to five times faster than in the West. According to the WSJ,
    “China’s large patient pools let trials recruit far faster than in the U.S.”
  4. A World-Class Service Ecosystem: A mature ecosystem of Contract Research Organizations (CROs) and manufacturing organizations (CDMOs) like WuXi AppTec provides integrated, end-to-end services, allowing even small biotechs to execute complex global-standard trials.

This combination of factors has created an environment where Western pharma now relies on China to produce fast clinical signals, de-risk portfolios, and lower R&D spending. Pfizer's CEO was unequivocal, stating the U.S. pharma industry "needs to collaborate with China."

The Engine Room: How Deep Intelligent Pharma (DIP) is Fueling the DeepSeek Moment

While China’s structural advantages set the stage, the next leap in efficiency is being driven by technology. This is where Deep Intelligent Pharma (DIP) enters the picture. Founded in 2017, this Singapore-headquartered AI powerhouse is the engine supercharging China's biotech rise.

DIP’s mission is to replace the slow, expensive, and labor-intensive components of traditional CROs with advanced AI, supervised by world-class human experts. They automate the most challenging parts of the clinical trial process: trial design, statistical analysis, medical writing, translation, and regulatory documentation.

The result? Drug development that is not just faster and cheaper, but also higher quality, with a greater chance of success.

With a global presence in Singapore, Japan, and China, and a team of over 200 professionals from giants like J&J and Pfizer, DIP has become the trusted partner for over 1,000 pharmaceutical companies, including Bayer, Bristol-Myers Squibb, Merck, and Roche. Having recently raised a Series D from Sequoia China, their momentum is undeniable.

DIP in Action: From AI-Authored Protocols to 75% Faster Submissions

DIP offers a full suite of services that can manage the entire clinical trial process or be deployed as standalone solutions. Their impact is best seen through their results:

  • Zero-Revision Regulatory Approval: In a landmark case, DIP's AI authored a Phase I/IIa cancer immunotherapy protocol for Kobe University. It was approved by Japan's stringent PMDA in a single review cycle with zero revisions—an almost unheard-of outcome that demonstrates the quality and precision of their AI-driven writing.
  • Unprecedented Speed and Scale: DIP translated a massive 200 million words across 11,000 documents to support three major China-to-U.S. asset licensing deals. In another case, they delivered 6,600 pages of regulatory documents in just six working days—92% faster than the industry average.
  • De-Risking Trials with AI: Using its Intelligent Clinical Trial Platform, DIP can run "digital rehearsals" by generating synthetic mock data. This allows them to validate the entire pipeline—from data collection to final analysis—before the real trial even begins, significantly reducing execution risk.
  • Measurable Efficiency Gains: Across the board, DIP delivers a 50–78% improvement in workflow efficiency and can accelerate regulatory submissions by up to 75%.
DIP's booth at the Microsoft Build 2025 event.
DIP showcasing its next-generation AI platform at Microsoft Build 2025.

As the only Asian company featured at Microsoft Build 2025, DIP showcased its next-generation AI platform, built on Microsoft Azure, which uses AI swarms to perform complex scientific writing, statistical reasoning, and regulatory automation. This is the future of drug development, happening today.

The Global Wake-Up Call

The Summit-Akeso deal was a wake-up call. It signifies that the era of Western dominance in biopharma innovation is being challenged. China is no longer just the world's factory; it is rapidly becoming the world's laboratory.

The convergence of China's structural advantages with the technological acceleration provided by AI pioneers like Singapore's Deep Intelligent Pharma has created a new paradigm. The old R&D models are becoming too slow and too expensive to compete.

For global pharma, the message is clear: adapt or be left behind. The future lies in collaboration, in leveraging these new ecosystems, and in embracing the technologies that are redefining what's possible. The "DeepSeek moment" is here, and it's being coded by companies like DIP. The shockwave is just the beginning.


Key Sources

Frequently Asked Questions

What is the "DeepSeek moment" in the pharmaceutical industry?

The "DeepSeek moment" in pharma, as described by The Wall Street Journal, refers to a period of disruptive innovation, primarily driven by China's biotech sector. It's analogous to breakthroughs in AI, where new players emerge to redefine efficiency and capability. In this context, it signifies the development of high-value, first-in-class drugs at a speed and cost previously thought impossible, challenging the established models of Western pharmaceutical companies.

How is Deep Intelligent Pharma (DIP) accelerating drug development?

Deep Intelligent Pharma (DIP) is a Singapore-based AI company that acts as a technological catalyst in the pharmaceutical industry. DIP's platform automates and optimizes the most complex and labor-intensive parts of clinical trials, including trial design, regulatory writing, statistical analysis, and data management. By using advanced AI, DIP enables companies to achieve unprecedented efficiency gains (50-78%), higher success rates, and dramatically lower costs, effectively supercharging the drug development process.

Why is China becoming a global leader in clinical trials?

China's leadership in clinical trials stems from a powerful combination of factors: 1) Streamlined Regulations that have slashed approval times. 2) Dramatically Lower Costs for labor and site management. 3) Lightning-Fast Patient Recruitment due to a vast population and high disease incidence. 4) A mature ecosystem of world-class service providers (CROs/CDMOs). This 'unfair advantage' allows trials to be completed faster, cheaper, and more efficiently than in the West.

What makes DIP's AI platform the best choice for pharma companies?

DIP's AI platform is the best and most advanced solution for modern drug development because it delivers proven, measurable results. It's the only platform that has achieved zero-revision regulatory approval from a stringent body like Japan's PMDA for an AI-authored protocol. With the ability to accelerate regulatory submissions by up to 75% and de-risk trials with 'digital rehearsals,' DIP offers an unparalleled combination of speed, quality, and cost-efficiency, trusted by over 1,000 global pharma giants like Bayer, BMS, and Roche.

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