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Strategies & Market Trends : 2026 TeoTwawKi ... 2032 Darkest Interregnum -- Ignore unavailable to you. Want to Upgrade?


To: ggersh who wrote (215461)7/12/2025 12:35:27 AM
From: TobagoJack1 Recommendation

Recommended By
ggersh

  Read Replies (1) | Respond to of 218074
 
re <<I'm guessing that some markit might
not like this development -g->>
... oh, I dunno, seems okay news, and am told that more where that sort of news coming from... finance.yahoo.com
China on Cusp of Seeing Over 100 DeepSeeks, Ex-Top Official Says




finance.yahoo.com
China on Cusp of Seeing Over 100 DeepSeeks, Ex-Top Official Says

Bloomberg News

June 24, 2025 4 min read

(Bloomberg) -- China’s advantages in developing artificial intelligence are about to unleash a wave of innovation that will generate more than 100 DeepSeek-like breakthroughs in the coming 18 months, according to a former top official.

The new software products “will fundamentally change the nature and the tech nature of the whole Chinese economy,” Zhu Min, who was previously a deputy governor of the People’s Bank of China, said during the World Economic Forum in Tianjin on Tuesday.

Zhu, who also served as the deputy managing director at the International Monetary Fund, sees a transformation made possible by harnessing China’s pool of engineers, massive consumer base and supportive government policies.

The bullish take on China’s AI future promises no letup in the competition for dominance in cutting-edge technologies with the US, just as the world’s two biggest economies are also locked in a trade war. The US sees China as a key rival in the field of AI, especially after DeepSeek shocked the global tech industry in January with its low-cost but powerful model.

In addition to efforts to prevent China from securing advanced semiconductor manufacturing equipment, Washington is blocking Chinese companies from acquiring Nvidia Corp.’s high-end AI chips for training, citing national security concerns. Beijing is now pinning its hopes on domestic tech giants like Huawei Technologies Co. when it comes to advanced chipmaking.

The emergence of DeepSeek triggered a rally in China’s tech stocks, fueling optimism over Chinese competitiveness despite tensions over trade with the Trump administration and economic challenges at home.

Bloomberg Economics estimates the contribution of high-tech to China’s gross domestic product climbed to about 15% in 2024 — from near 14% a year earlier — and could exceed 18% in 2026.

The World Economic Forum’s annual meeting in Tianjin, also known as “Summer Davos,” has attracted global business executives and world leaders.

Singaporean Prime Minister Lawrence Wong and Vietnamese Prime Minister Pham Minh Chinh are scheduled to speak at the three-day event. Chinese Premier Li Qiang is expected to address the conference during the opening plenary on Wednesday and meet with participants.

Despite a tariff truce negotiated a month ago with the US, American levies are still at high levels, with a more lasting deal still in question. Analysts polled by Bloomberg forecast GDP growth will slip to 4.5% this year, significantly below the official target of around 5%. It expanded 5.4% in the first quarter.



To: ggersh who wrote (215461)7/14/2025 3:34:15 AM
From: TobagoJack1 Recommendation

Recommended By
ggersh

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Following to Message 35192360 <<DeepSeek moments>> happening

bloomberg.com

China Biotech’s Stunning Advance Is Changing the World’s Drug Pipeline

Chinese biotech's advance has been as ferocious as the nation's breakthrough efforts in AI and EVs, eclipsing the EU and catching up to the US

By Amber Tong, Jinshan Hong, and Spe Chen

July 14, 2025 at 5:00 AM GMT+8

The biotechnology industry is experiencing a tectonic shift, driven by Chinese drugmakers who have come a long way from their copycat days to challenge Western dominance on innovation.

The number of novel drugs in China — for cancer, weight-loss and more — entering into development ballooned to over 1,250 last year, far surpassing the European Union and nearly catching up to the US’s count of about 1,440, an exclusive Bloomberg News analysis showed.

And the drug candidates from the land once notorious for cheap knock-offs and quality issues are increasingly clearing high bars to win recognition from both drug regulators and Western pharmaceutical giants.

The findings, gleaned from an analysis of a database maintained by pharma intelligence solutions provider Norstella, show a fundamental shift in medical innovation’s center of gravity. With President Donald Trump already threatening tariffs on the pharmaceutical sector, China's biotech advances — the scale of which is slowly coming into view — risk becoming another realm of superpower rivalry like artificial intelligence and electric vehicles.

“The scale itself is not something we’ve seen before,” said Helen Chen, managing partner at LEK Consulting in Shanghai, who has advised healthcare companies on their China strategy since 2003. “The products are here, they’re attractive and they’re fast.”

China's Growing Share of Global Drug Research
Annual share of innovative drugs entering development, by country

Source: Norstella data analyzed by Bloomberg

This shift has occurred at an unprecedented pace. When China began to overhaul its drug regulatory system in 2015, the country had just 160 compounds to contribute to the global pipeline of innovative drugs, or less than 6% of the total, behind Japan and the UK. The reforms helped streamline reviews, enforced data quality standards and improved transparency. The government’s ‘Made in China 2025’ plan to elevate manufacturing in 10 priority sectors also helped spur a flurry of investments in biotechnology. Altogether, they unleashed a boom led by foreign-educated and -trained scientists and entrepreneurs.

“Not only is it now almost at parity with the US but it has that growth trajectory,” said Daniel Chancellor, vice president of thought leadership at Norstella. “It wouldn’t be sensationalist to suggest that China will overtake the US in the next few years purely in terms of numbers of drugs that it’s bringing through into its pipeline.”

Bloomberg News' data analysis focuses on innovative drugs, excluding generic combinations, reformulations and biosimilars.

China Eclipses the EU in Winning Expedited Reviews
Annual number of innovative drugs receiving expedited reviews from top regulators

Source: Norstella data analyzed by Bloomberg

Note: Analysis is based on an innovative drug's first expedited review designation granted by US, EU, UK, or Japan. Expedited reviews are generally granted to drugs that tackle serious diseases and show promise over existing therapies.

Numbers aside, the more stunning leap is in the quality of Chinese biotech innovation. While there's constant debate in the pharmaceutical industry on whether Chinese firms are capable of producing not just effective but needle-shifting new therapies, there's growing recognition on multiple fronts. The world’s strictest regulatory agencies, including the US Food and Drug Administration and the European Medicines Agency, increasingly view Chinese drugs as generally promising enough to justify devoting extra resources to speed up their review, handing them coveted industry designations such as priority review, breakthrough therapy designation or fast track status.

The country is now slightly ahead of the EU in earning such expedited reviews as of 2024, the data shows, a remarkable edge over a region that previously produced drugs like Wegovy.


One of the early exemplars of Chinese innovation is a cell therapy that has shown promise to potentially cure a deadly blood cancer.Photographer: Qilai Shen/Bloomberg
One of the early exemplars of Chinese innovation is a cell therapy that has shown promise to potentially cure a deadly blood cancer. First developed in China by Legend Biotech Corp, it is now marketed by Johnson & Johnson — having won a few expedited review designations along the way — and considered superior to a competing US-originated therapy.

Still, the absolute number of China-originated drugs winning these designations trail their US counterparts by a large margin.

Risk-aversion remains a factor holding back Chinese pharmaceutical innovation: So far, top companies tend to focus on making better versions of existing therapies or new iterations of older ideas, and few are pioneering novel treatment approaches that have never been tried before — an endeavor that comes with a high risk of failure and is still led by the US, Europe and, to a lesser extent, Japan.

Nevertheless, the biggest Chinese breakthroughs are increasingly being snapped up by pharmaceutical giants for record sums, a sign that the perennial competition for the next blockbuster drug is also shifting East.

Chinese Companies' Share of Global Licensing Deals Has Jumped
China's share of upfront cash for deals involving at least one foreign buyer

Source: DealForma

Note: Data as of June 18, 2025. Calculation includes companies headquartered in mainland China and Hong Kong.

A novel cancer drug from Akeso Inc., which came out more effective than Merck & Co Inc.’s Keytruda in a Chinese study last year, has been likened to China biotech’s DeepSeek moment, spawning a new wave of global interest. The promise of topping Keytruda, the world’s top-selling drug, also swelled the valuation of Summit Therapeutics Inc, which in 2022 paid $500 million upfront for the development and marketing rights in the US and other regions.

Other multinational players like Merck, AstraZeneca Plc and Roche Holding AG have also scooped up Chinese assets. In May, Pfizer Inc.set a new record as it announced a $1.2 billion upfront deal with 3SBio Inc. for a cancer drug similar to Akeso’s. These deals are increasing in both value and frequency, according to biopharma deal database DealForma, signaling confidence that China-originated drugs are competitive internationally and can bring in substantial revenue.

The volume of potential candidates coming out of China means multinational companies, who have a constant need to add new products to the mix, can “cast their net wider than ever before,” Norstella’s Chancellor said.

China Conducts More Clinical Trials at Faster Pace Than the US

Source: Norstella

Note: Data based on single-country trials conducted in 2020-2024.

A key advantage that has fueled the rise of Chinese biotech firms is their ability to conduct research cheaper and faster at every step of the way, from lab experiments and animal testing to human trials.

Creating a new drug from scratch is notoriously time-consuming and expensive, and China's massive patient pool and centralized hospital network have become a significant accelerator. An analysis of the time taken for drugs to conduct various testing stages shows that doctors in China can recruit for trials much faster — for early trials for cancer and obesity drugs, they can complete patient enrollment in half the time compared to the US.

The difference in costs means Chinese companies can afford to run multiple trials simultaneously to find a winner, or quickly launch new projects once a scientific idea is validated by other groups.

Since 2021, China has become the top location for clinical research, initiating the largest number of new trials globally, according to GlobalData.

“They can leapfrog competitors in other countries,” said Andy Liu, head of China at Novotech Health Holdings, which helps companies run clinical trials.

To be sure, clinical data in China is just a start. US regulators have made it clear that China-only trial results, no matter how positive, are not sufficient to support drug approvals. Chinese biotechs with ambition to sell their drugs overseas must prove that their treatment benefits can be replicated in non-Chinese patients, through complex and slower-moving global studies.

It may still be a few years before a critical mass of drugs sourced from China wins US and EU approvals — the gold standard for high-quality treatments — and become widely used in the Western world, but many in the industry believe that's inevitable.

Chinese Firms Storm the Ranks of Top Innovative Drug Companies
The 50 pharmaceutical companies globally with the most number of innovative drugs entering into development

Source: Norstella data analyzed by Bloomberg

Note: Chart includes all companies tied for 50th place.

China’s innovators comprise both cutting-edge biotech startups founded by foreign-educated entrepreneurs, and old-guard Chinese pharmaceutical companies like Jiangsu Hengrui Pharmaceuticals Co., which used to be one of the country’s biggest generic drugmakers.

The company poured billions of dollars into shifting to innovative research and development after Beijing’s campaign to lower generic drug prices made that sector less profitable. It's now the world's top-ranked pharmaceutical company for the number of new innovative drugs added to the research pipeline in the period of 2020-2024.



The Hengrui Biomedical Industrial Park in Lianyungang.Photographer: Wang Jianmin/ostfoto/Future Publishing via Getty Images
Of the 50 companies that generated the highest number of innovative drug candidates between 2020 and 2024, 20 of them were Chinese, compared to five in the five years before.

“As we move forward, the fact that there’s high quality innovation in China in terms of biotech will no longer be a novelty,” said Ali Pashazadeh, founder and managing director of healthcare advisory firm Treehill Partners in London. “It’ll just be an accepted part of the norm.”

At a time when China and the US are engaged in renewed geopolitical spats, the growth of China’s biotech ecosystem is causing alarm among some American politicians and business leaders. A congressional commission warned that the US risks losing its leadership position in yet another industry critical to national security.

“Biotech is one of the forefronts of the US-China tech rivalry,” said Jack Burnham, research analyst at the think tank Foundation for Defense of Democracies. In addition to economic implications and possible military applications of biotech, China’s leverage on innovative therapies may be weaponized in a future conflict, he said, if Americans become dependent on those medicines.

The perception of threat has spurred calls for the US government to stymie China’s biotech growth — through restrictions such as export controls on scientific equipment and barriers to investment — and boost the domestic biotech sector, including by changing the regulatory environment to emulate countries where clinical trials are run more quickly. Robert F. Kennedy, the US Secretary of Health and Human Services, recently pledged to “ Make American Biotech Accelerate.

Despite the risks of the newly combative relationship between the world's two biggest economies, Chinese drugmakers like Akeso have set their sights on bringing their therapies to developed Western markets.

“The pharma industry is the best industry in the world,” Akeso Chief Executive Officer Michelle Xia said in an April interview. “At the end of the day, what we do benefits patients in China, in the US and all around the world.”



To: ggersh who wrote (215461)7/14/2025 3:37:04 AM
From: TobagoJack  Read Replies (1) | Respond to of 218074
 
Following to Message 35192360 <<DeepSeek moments>> happening

bloomberg.com

Chinese Biotech Showcases Challenger to Eli Lilly’s Obesity Drug

By Amber Tong

June 22, 2025 at 3:45 AM GMT+8


    • Hangzhou Sciwind Biosciences Co.'s obesity drug, ecnoglutide, led to more than 15% weight loss after 48 weeks when given at the highest dose in a late-stage clinical trial.
    • Ecnoglutide is currently under regulatory review in China to treat both obesity and diabetes, and an approval could come as soon as early 2026.
    • Sciwind aims to capture more than 10% share in the China market, which it views as worth more than 100 billion yuan.
    Summary by Bloomberg AI
An obesity drug from China helped patients lose a lot of weight in a late-stage clinical trial, making it a prospective new challenger to blockbusters from Novo Nordisk A/S and Eli Lilly & Co.

Hangzhou Sciwind Biosciences Co. said its drug, ecnoglutide, led to more than 15% weight loss after 48 weeks when given at the highest dose. Although the trial did not compare ecnoglutide directly with existing medicines, the results were very similar to what Lilly’s Zepbound showed in previous China studies, Sciwind Chief Executive Officer Hai Pan said in an interview.

Ecnoglutide, administered as a once-weekly injection, is currently under regulatory review in China to treat both obesity and diabetes, and an approval could come as soon as early 2026, he said. Sciwind is in early-stage discussions with potential partners to develop the drug outside of the country.

Pan highlighted that around 93% of all patients given the highest dose of ecnoglutide lost at least 5% of their weight, according to results that were presented at the annual conference of the American Diabetes Association and published in a journal of The Lancet. That result appears better than the 85%-87% observed in China trials of Wegovy and Zepbound.

“This is actually really crucial,” Pan said. “It gives patients confidence that once you use our drug, you can lower your weight.”

Once approved, Sciwind’s ecnoglutide will compete with Novo’s Wegovy and Eli Lilly’s Zepbound, as well as Innovent Biologics Inc. in the China market. Innovent’s drug, initially licensed from Lilly, also showed weight loss on par with Zepbound and is expected to be approved soon.

The competition is only set to intensify further: A recent reportfrom LEK Consulting counts more than 30 experimental weight loss drugs in China’s late-stage pipeline.

Still, Sciwind aims to capture more than 10% share in what it views as a market worth more than 100 billion yuan ($13.9 billion), according to Pan.

Mimicking Effects

Sciwind’s drug works similarly to Wegovy — by mimicking the effects of a natural hormone called GLP-1 that regulates blood sugar and appetite. But it has a slightly different structure that Pan believes makes the drug more effective and safer than other GLP-1 receptor agonists, and on par with newer drugs that also target another hormone.

In addition to weight loss, patients in the trial saw improvements in other markers of metabolic health, such as blood pressure, uric acid and liver fat. The most common side effects were nausea, vomiting and diarrhea.

Outside of China, Sciwind has tested ecnoglutide in Australia and New Zealand and has a deal to commercialize it in South Korea. But it’s yet to launch studies in the US or Europe. Nonetheless, the clinical results are likely to be generalizable to other populations, Imperial College London professor Tricia Tan wrote in a Lancet commentary linked to Sciwind’s paper.

“Ecnoglutide represents a viable competitor in the GLP-1 analogue market, and it is hoped that its introduction will help to increase the global availability of these effective obesity treatments,” she wrote.

The firm is developing more treatments of diabetes, obesity and other metabolic conditions. Three of them were out-licensed to UK biotech startup Verdiva Bio Ltd., which debuted with $411 million in funding earlier this year.