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BioWorld - Wednesday, July 1, 2026
Home » Topics » Asia-Pacific, BioWorld Asia

Asia-Pacific, BioWorld Asia
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Handshake behind digital globe

Everest to acquire Singapore unit of Hasten Bio in $250M deal

April 14, 2026
By Marian (YoonJee) Chu
No Comments
Everest Medicines Ltd. has agreed to acquire a Singapore-based commercial unit of Hasten Biopharmaceuticals (Asia) Ltd. for $150 million up front, gaining market authorization holder rights to 14 marketed products originally developed by Takeda Pharmaceutical Co. Ltd.
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Drug research illustration

Biologics in development outnumber small molecules for the first time

April 14, 2026
By Nuala Moran
No Comments
More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&D pipeline.
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Gold wireframe handshake
Biopharma deals March 2026

Biopharma deal value gains 17% in early 2026

April 14, 2026
By Amanda Lanier
No Comments
Biopharma deal value totaled $18.05 billion in March 2026, a pullback from $30.01 billion recorded in February and $31.16 billion in January, but broadly in line with prior years. The March total exceeds March 2024 ($8.5 billion) and is comparable to March 2023 ($19.68 billion) and 2022 ($15.35 billion). For the first quarter (Q1) 2026, deal value increased 17% year over year to $79.22 billion, up from $67.6 billion in Q1 2025.
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Open capsule delivering pain relief to body

Abbvie nabs two Nav1.8 pain projects from Haisco in $745M deal

April 14, 2026
By Marian (YoonJee) Chu
No Comments
Abbvie Inc. is buying exclusive rights to develop, manufacture and commercialize two Nav1.8 inhibitors for pain – HSK-55718 and HSK-51155 – from Haisco Pharmaceutical Group Co. Ltd. for $30 million up front and up to $715 million in milestone payments, plus royalties.
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Brain scans

FDA accepts Telix’s resubmitted NDA for brain imaging agent

April 10, 2026
By Tamra Sami
No Comments
The U.S. FDA has accepted for review Telix Pharmaceuticals Ltd’s resubmitted NDA for TLX101-Px (Pixclara, 18F-floretyrosine, 18F-FET), its radiolabeled glioma imaging product for characterizing progressive or recurrent glioma in adult and pediatric patients. The FDA assigned a Sept. 11, 2026, PDUFA date.
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Drug vials and syringe

South Korea streamlines biosimilar review, clinical trials

April 7, 2026
By Marian (YoonJee) Chu
No Comments
South Korea is rolling out regulatory changes to speed biosimilar development, including reforms to shorten review timelines, ease phase III trial requirements and simplify oversight of manufacturing changes. 
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Illustration of cancer in the pancreas

Amplia halts enrollment in phase II pancreatic cancer trial

April 7, 2026
By Tamra Sami
No Comments
Amplia Therapeutics Ltd. has halted recruitment in its phase II Amplicity trial in advanced pancreatic cancer due to three dose-limiting toxicities related to the chemotherapy regimen, modified FOLFIRINOX (mFOLFIRINOX), which is being administered in combination with lead compound narmafotinib (AMP-945), a focal adhesion kinase inhibitor.
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Digital globe illustrating pharma trade, tariffs

Sector tariff now more than a threat – for some Rx companies

April 7, 2026
By Mari Serebrov
No Comments
After nearly a year of threats and promises of a global biopharma tariff of 25% to 500%, U.S. President Donald Trump finally delivered it. In the name of national security, he imposed a 100% sector tariff on prescription drugs and their associated ingredients beginning in about four months for large manufacturers and six months for smaller companies.
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PET scans showing before and after treatment with VIPOR
ICKSH 2026

Five-drug VIPOR regimen shows promise in aggressive blood cancer

April 7, 2026
By Marian (YoonJee) Chu
No Comments
Deep molecular advances are enabling precision medicine for the field of hematology, Wyndham Wilson said during a plenary session at the 2026 Korean Society of Hematology International Conference March 26.
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Pill in immersive interface

Lilly taps Insilico AI in $2.75B deal to expand pipeline options

March 31, 2026
By Tamra Sami
No Comments
Eli Lilly and Co. is deepening its investment in artificial intelligence-driven drug discovery through a multibillion-dollar expansion of its collaboration with Hong-Kong listed Insilico Medicine Inc. in a move that could broaden its reach into next-generation metabolic therapies. Under the deal terms, Insilico is eligible to receive $115 million up front, plus development, regulatory, and commercial milestone payments worth $2.75 billion, in addition to sales-based royalties. In exchange, Lilly gains exclusive global rights to develop and commercialize multiple candidates generated using Insilico’s AI platform, including preclinical oral therapies.
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