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Singapore biomedical startups are expanding into China to accelerate the development of new treatments for cancer and diabetes. A*STAR spin-offs Lion TCR and Be…
Singapore biomedical startups are expanding into China to accelerate the development of new treatments for cancer and diabetes. A*STAR spin-offs Lion TCR and BetaLife are tapping China's vast patient pool, hospital networks and manufacturing capabilities to advance clinical trials and research. But navigating the country's evolving biomedical regulations remains a challenge. Enterprise Singapore is helping firms understand new approval pathways and build partnerships, with hopes that these innovations could eventually benefit patients back home. Ivy Chok reports.
China has reached parity with the United States in the sheer volume of biomedical research output and early-stage drug pipelines, while the U.S. continues to maintain a lead in research influence, high-impact citations, and cutting-edge breakthrough discoveries.
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<br>Research Volume and Early-Stage Pipelines.
<br>• Publication & Output: China has matched or surpassed the U.S. in total scientific publishing and annual biomedical research output, with top institutions in both countries producing roughly 43,500 papers a year, and China accounting for over 32% to 40%+ of global medical research papers.
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<br>• Early-Stage Drug Development: According to data published in JAMA, China's share of global early-stage drug development programs surged from 8% in 2015 to over 32% by 2024, whereas the U.S. share shifted from 48% down to roughly 37%.
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<br>• Speed & Cost Advantages: Clinical trials and first-in-human studies often move significantly faster and at lower costs in China due to large patient populations and streamlined local processes, prompting a surge in cross-border licensing deals where Western pharma companies license Chinese-developed compounds
Singapore biomedical startups are expanding into China to accelerate the development of new treatments for cancer and diabetes. A*STAR spin-offs Lion TCR and BetaLife are tapping China's vast patient pool, hospital networks and manufacturing capabilities to advance clinical trials and research. But navigating the country's evolving biomedical regulations remains a challenge. Enterprise Singapore is helping firms understand new approval pathways and build partnerships, with hopes that these innovations could eventually benefit patients back home. Ivy Chok reports.
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Singapore biomedical startups expanding into China to accelerate cancer and diabetes treatments
Galina Kaczmarek • 2.1K views
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<br>
<br>Research Volume and Early-Stage Pipelines.
<br>• Publication & Output: China has matched or surpassed the U.S. in total scientific publishing and annual biomedical research output, with top institutions in both countries producing roughly 43,500 papers a year, and China accounting for over 32% to 40%+ of global medical research papers.
<br>
<br>• Early-Stage Drug Development: According to data published in JAMA, China's share of global early-stage drug development programs surged from 8% in 2015 to over 32% by 2024, whereas the U.S. share shifted from 48% down to roughly 37%.
<br>
<br>• Speed & Cost Advantages: Clinical trials and first-in-human studies often move significantly faster and at lower costs in China due to large patient populations and streamlined local processes, prompting a surge in cross-border licensing deals where Western pharma companies license Chinese-developed compounds