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BioWorld - Thursday, January 1, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

June 18, 2024

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Illustration of intestines with inflammation

Futuregen joins Abbvie in $1.7B inflammatory bowel disease deal

Through a global rights agreement with Futuregen Biopharmaceutical Co. Ltd., Abbvie Inc. continues to build its immunology portfolio to help offset losses from Humira as biosimilars tighten their grip on the mega-blockbuster. Read More

Imbiologics nets $20M up front for Navigator autoimmune drug

South Korea’s Imbiologics Inc. scored a potential $940 million (₩1.3 trillion) technology transfer deal with U.S. biotech Navigator Medicines Inc. for its bispecific antibody drug candidate, IMB-101 (Oxtima), to treat autoimmune diseases. Read More
Handshake_global2.png

Takeda, Ascentage in $1.2B option agreement for olverembatinib

Takeda Pharmaceutical Co. Ltd. has signed an option agreement to in-license Ascentage Pharma Group Inc.’s olverembatinib, an oral third-generation BCR-ABL tyrosine kinase inhibitor (TKI). If exercised, the option would allow Takeda to license exclusive global rights to develop and commercialize olverembatinib in all territories outside of mainland China, Hong Kong, Macau, Taiwan and Russia. Read More
Health Minister Mark Butler, Ternarx CEO Joanne Boag and WEHI Director Ken Smith

Ternarx exits stealth with focus on targeted protein degraders

Fledgling biotech Ternarx Pty Ltd. has emerged from stealth mode and is the first of its kind in Australia to develop targeted protein degrader technology to destroy disease-causing proteins that cannot be targeted by conventional drugs. The Melbourne-based company will initially develop targeted protein degraders against currently undrugged transcription factors in cancers with significant unmet need, starting with neuroblastoma and prostate cancer. Read More
Australian coins and bills

Opthea raising AU$227M, enters final phase III stretch for OPT-302

Opthea Ltd. announced it plans to raise up to AU$227.3 million (US$150 million) to extend its cash runway through the data readout for its two phase III pivotal trials of sozinibercept (OPT-302) in wet age-related macular degeneration. Read More
Xtalpi lab

China’s AI-powered Quantumpharm raises $126M in Hong Kong IPO

Chinese artificial intelligence (AI)-driven drug discovery firm Quantumpharm Inc., also known as Xtalpi, began trading on the Hong Kong stock exchange June 13, listing under a new special technology listing track that lured it away from an IPO in the U.S. Read More
Epileptic brain and abnormal EEG wave discharges

Ovid takes hit on phase III epilepsy failures in Takeda venture

Disappointing top-line data from two failed phase III studies of soticlestat for Dravet syndrome (DS) and Lennox-Gastaut syndrome (LGS) have crumpled the stock of co-developer Ovid Therapeutics Inc., which lost three-quarters of its value June 17. Read More

No Nasdaq for now: Radiopharma firm Telix pulls US IPO

A week after generating buzz with its proposed Nasdaq listing and plans to raise about $200 million, Telix Pharmaceuticals Ltd. withdrew its U.S. IPO filing, citing market conditions. The Australian radiopharma firm’s shares continue trading on the Australian Securities Exchange (TLX), where they closed June 14 at AU$16.61 (US$10.98), up AU15 cents.

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Celltrion seeks US IND nod for Keytruda biosimilar phase III

As competition rises in the Keytruda (pembrolizumab) biosimilar space, Celltrion Inc. is the latest to announce that it filed an IND application to the U.S. FDA to start a global phase III trial for its own Keytruda biosimilar, dubbed CT-P51. Incheon, South Korea-based Celltrion, which previously said it would differentiate from the pack by developing an easier-to-administer subcutaneous biosimilar of pembrolizumab, announced June 17 plans to start a global comparative phase III study of CT-P51 and Keytruda. Read More

May biopharma deals hit $18.76B, up 23% from April

Biopharma deal value surged in May to $18.76 billion, up 23% from April's $15.28 billion. This increase follows March’s $8.29 billion and February’s $7.76 billion, although represents a decline from January’s $27.9 billion. The monthly average for 2024 stands at $15.64 billion, compared to the $18.14 billion monthly average in 2023. Meanwhile, the value of biopharma M&As rose to $4.75 billion in May, an increase from April’s $1.33 billion, which was the lowest figure in nearly a year. Read More

Biosecure Act misses first congressional ride

The Biosecure Act missed its first chance at a congressional ride June 11 when the U.S. House Rules Committee didn’t include it, as many had expected, on the list of potential riders the House will consider for its version of the National Defense Authorization Act, a must-pass defense spending bill for fiscal 2025. But that doesn’t mean the bill will be stranded by the wayside. Read More

Appointments and advancements for June 18, 2024

New hires and promotions in the med-tech industry in Asia-Pacific, including: Zai Lab. Read More

Financings for June 18, 2024

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

In the clinic for June 18, 2024

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Biosion, Gannex, Junshi. Read More

Other news to note for June 18, 2024

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: Deciphera, Dong-A, Hudson, Ono, Shaperon. Read More

Regulatory actions for June 18, 2024

Regulatory snapshots, including drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations in Asia-Pacific: Ascentage, Belite, Bioarctic, GC Biopharma, Innovent, Santhera. Read More

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