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BioWorld - Wednesday, April 22, 2026
Home » Topics » Regions » Asia-Pacific

Asia-Pacific
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Scinopharm wins US FDA approval of multiple sclerosis drug

Jan. 5, 2026
By Marian (YoonJee) Chu
No Comments
Scinopharm Taiwan Ltd. received U.S. FDA approval for its generic version of glatiramer acetate injection, a treatment for multiple sclerosis.
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AI biotech research concept with lightbulb and digital background

Insilico inks $888M drug discovery partnership with Servier

Jan. 5, 2026
By Tamra Sami
No Comments
After raising $292 million in its Hong Kong IPO, AI discovery and development biotech, Insilico Medicine, signed an R&D collaboration with French pharma Servier SA valued at $888 million to discover and develop innovative oncology therapies by combining Insilico's AI-driven drug discovery platforms with Servier's global expertise in cancer drug development.
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Map of Australia as blue circuit board, digital network

TGA eyes do-over for conformity assessment procedures

Jan. 5, 2026
By Mark McCarty
Australia’s Therapeutic Goods Administration posted a proposed rework of the agency’s conformity assessment procedures that would align with EU regulations, but the agency stated clearly that it is aware of some of the hazards of further alignment with the troubled European regulations.
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3D illustration of T cells fighting cancer

New year sees Abbvie, Zelgen in $1.1B T-cell engager deal

Jan. 2, 2026
By Tamra Sami
No Comments
Abbvie Inc. signed a $1.1 billion New Year’s Eve deal with China’s Zelgen Biopharmaceuticals Co. Ltd., gaining ex-China rights to Zelgen’s lead oncology asset, alveltamig (ZG-006), a trispecific T-cell engager targeting delta-like ligand 3. Under terms of the deal, Abbvie will pay Zelgen an up-front fee of $100 million, and Zelgen is eligible to receive $60 million in near-term milestones and could receive up to $1.075 billion in additional development, regulatory and commercial milestones, alongside tiered royalties on net sales outside China. Zelgen retains full rights in China.
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Shenzhen Edge Medical Co. Ltd.’s Multi-Port Endoscopic Surgical Robot

Surgical robotic maker Shenzhen Edge announces $154M HKEX IPO

Dec. 31, 2025
By Tamra Sami
Surgical robotics maker Shenzhen Edge Medical Co. Ltd. reported its initial public offering on the Hong Kong Stock Exchange to raise HKD$1.19 billion (US$154 million) to advance its pipeline of surgical robotic systems and expand its geographic footprint to markets outside China.
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IPO line graph
Year in review

Med-tech IPOs shoot for the stars in 2025

Dec. 31, 2025
By Annette Boyle
IPOs top the list of the big stories in 2025 in med tech. Thirty med-tech companies went public, raising nearly $12 billion, two orders of magnitude more than in 2023 and almost 20 times more than raised in 2024.
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Advanced Biomed’s A+Perfusc 3D cell culture system

Advanced Biomed sells Hong Kong subsidiary for $23k

Dec. 31, 2025
By Marian (YoonJee) Chu
Advanced Biomed Inc. reported Dec. 30 the sale of its wholly owned Hong Kong subsidiary, Advanced Biomed (HK) Ltd., and related intellectual property to buyer Wei Ha Hui for $23,000.
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India map on technology concept background
Diagnostics

Bayosthiti AI to build India-specific RNA sequencing ecosystem

Dec. 31, 2025
By Marian (YoonJee) Chu
Bayosthiti AI Pvt Ltd. aims to make RNA sequencing and AI-based preventive health care affordable and accessible for the Indian market, leveraging intellectual property from its parent company, Biostate AI Inc.
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Globe isolated on white background with focus on Asia and Australia
The year in review

Investment pays off as Asia shapes global biotech trends in 2025

Dec. 30, 2025
By Tamra Sami
No Comments
Asia, led by China, is no longer just following global pharma trends. It is helping to shape them, and for investors, innovators and policymakers, the question is no longer whether to engage with Asia, but how to engage wisely in this new, more complex world.
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Liver illustration

China accepts Hutchmed fanregratinib NDA on single phase II trial

Dec. 30, 2025
By Tamra Sami
No Comments
Hutchmed (China) Ltd. has moved closer to establishing China’s first domestically developed FGFR-targeted therapy for intrahepatic cholangiocarcinoma, after the National Medical Products Administration (NMPA) accepted its NDA for fanregratinib (HMPL-453) and granted the drug priority review.
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