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BioWorld - Wednesday, March 11, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

March 18, 2025

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Rendering of Alteogen’s ALT-B4

Alteogen in $1.35B Medimmune deal; Astrazeneca bids $1B for Esobiotec

Alteogen Inc. signed its first billion-dollar partnership this year for ALT-B4 technology through two separate contracts with Astrazeneca plc’s U.K.- and U.S.-based Medimmune subsidiaries worth up to $1.35 billion combined. Read More
Gold dollar sign inside gold cog

Taiho acquiring Araris in $1.14B ADC deal

The antibody-drug conjugate (ADC) juggernaut powers on, with Japan’s Taiho Pharmaceutical Co. set to acquire Araris Biotech AG for up to $1.14 billion. Of that, $400 million will be up front, with the remainder tied to milestones with a maximum value of $740 million, around the progress of three ADCs for treating solid and hematological cancers. Read More
Insilico Medicine CEO Alex Zhavoronkov with Insilico’s first bipedal humanoid AI Scientist called “Supervisor.”

Insilico advancing AI platform with $110M Asian-backed series E round

Artificial intelligence (AI) drug developer Insilico Medicine raised $110 million in a series E round led by an Asian private equity fund, Value Partners Group, that will see Insilico advance its pipeline and AI platform developments. Read More

Ono scoops Ionis' hematology candidate sapablursen for up to $940M

Ono Pharmaceutical Co. Ltd. struck a licensing deal with Ionis Pharmaceuticals Inc. for sapablursen, which is in phase II trials for polycythemia vera. Under terms, Osaka, Japan-based Ono gains an exclusive license to develop and commercialize sapablursen worldwide. Carlsbad, Calif.-based Ionis will be responsible for completing the ongoing phase II Imprssion study, while Ono will be responsible for subsequent development, regulatory filings and commercialization. Read More
Colorized scanning electron microscope image of regulatory T cells and antigen-presenting cells.

Japan’s Regcell launches in US with $45.8M to advance Treg platform

Japanese-founded Regcell Inc. has raised $45.8 million and is redomiciling to the U.S. to accelerate clinical development of its pioneering regulatory T-cell (Treg) platform for autoimmune diseases and transplantation. Read More

China accepts NDA of influenza tablet, clears Tepezza biosimilar

China’s National Medical Products Administration (NMPA) approved the country’s first injectable teprotumumab biosimilar from Innovent Biologics Inc. under the brand name of Sycume (teprotumumab N-01) to treat thyroid eye disease on March 14. The NMPA on March 15 accepted Simcere Pharmaceutical Group Ltd.’s NDA of deunoxavir marboxil (ADC-189) tablets, a product originally developed by Jiaxing Andicon Biotech Co. Ltd. to treat influenza A and B. Read More

Visen announces HKD$603M Hong Kong IPO

Visen Pharmaceuticals Co. Ltd. announced its initial public offering (IPO) on the Hong Kong Stock exchange (HKEX) to raise roughly HKD$603.3 million (US$77.6 million) to advance its pipeline of endocrinology assets. Read More
covid-19-coronavirus-lungs

Healios posts more upbeat data on Multistem cell therapy for ARDS

Latest findings on Healios K.K.’s stem cell therapy to treat acute respiratory distress syndrome (ARDS), coined Multistem (invimestrocel; HLCM-051), found the regenerative medicine effective in reducing the number of patient days on ventilator treatment, as well as mortality benefits. Read More

Celltrion wins FDA approval of denosumab, omalizumab biosimilars

Celltrion Inc. is on a biosimilar roll with the U.S. FDA this month, having gained clearance of Stoboclo and Osenvelt as products referencing Amgen Inc.’s biologic, denosumab (Prolia, Xgeva), along with Omlyclo becoming the first and only interchangeable biosimilar to omalizumab (Xolair, Genentech Inc. and Novartis AG). Read More
Vaccine vial and syringe

Aim seeks approval of first serum-free human rabies vaccine

Aim Vaccine Co. Ltd. may become the first company to gain regulatory clearance of a prophylactic iterative serum-free human rabies vaccine. Beijing-based Aim said it is preparing a regulatory submission of its independently developed rabies vaccine based on positive phase III results that showed good safety, immunogenicity and immune persistence. Read More
Red coronavirus with long shadow

Long COVID science is progressing, though therapies have not yet followed

In 2020, the Conference on Retroviruses and Opportunistic Infections (CROI) was the first scientific conference to move from in-person to virtual due to the COVID-19 pandemic. On the fifth anniversary of the virtual conference, and the pandemic, some of those earliest COVID-19 patients have still not recovered. Read More
Puzzle-pieces-globe.png

GSK’s $1.15B Idrx buyout leads slow M&A market as deals stay strong

Biopharma deal activity climbed in early 2025, reaching $37.38 billion in the first two months, up from $35.66 billion a year ago. February saw $8.76 billion in deals, down 69% from January’s $28.63 billion, which included 11 transactions valued at $1 billion or more. Early 2025 saw the second-highest biopharma deal total on record, trailing only the $42.19 billion logged in the first two months of 2022. Read More

Financings for March 18, 2025

Biopharmas in Asia-Pacific raising money in public or private financings: Accropeutics. Read More

In the clinic for March 18, 2025

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Ascletis, Innocare, Shionogi. Read More

Other news to note for March 18, 2025

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: Biocon, Daiichi Sankyo, Nosis, SK Bioscience. Read More

Regulatory actions for March 18, 2025

Regulatory snapshots, including drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations in Asia-Pacific: Celltrion, H. Lundbeck, Innovent, Lupin, Otsuka, Taro, Zai Lab. Read More

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