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BioWorld - Saturday, February 14, 2026
Home » Topics » U.S., BioWorld Asia

U.S., BioWorld Asia
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Head and neck anatomy

Real-world data illuminates Rakuten's Alluminox solid tumor platform

Sep. 26, 2025
By Marian (YoonJee) Chu
No Comments
Rakuten Medical Inc. is advancing a pipeline of solid tumor therapeutics built on its Alluminox platform worldwide, having gained conditional early approval of ASP-1929, an Alluminox-derived photoimmunotherapy, in Japan in 2020.
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Red blood cells in an artery with cholesterol

Kalexo enters dyslipidemia fray with preclinical siRNA candidate

Sep. 23, 2025
By Marian (YoonJee) Chu
Mabwell Bioscience Co. Ltd. and Aditum Bio Management Co. LLC announced, in after-market hours Sept. 17, an agreement to forge a new company called Kalexo Bio Inc. and load the biotech with a preclinical dyslipidemia asset via a potential $1 billion global license deal.
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Keytruda Qlex

US FDA clears ‘one-minute’ Keytruda SC injection for solid tumors

Sep. 23, 2025
By Marian (YoonJee) Chu
No Comments
The U.S. FDA approved Merck & Co. Inc.’s Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph) injection on Sept. 19, making it the first and only subcutaneously (SC)-administered immune checkpoint inhibitor that can be administered in about a minute.
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Celltrion building and skyline

Celltrion to buy Lilly’s cGMP plant for $330M, invest up to $1B

Sep. 23, 2025
By Marian (YoonJee) Chu
No Comments
Celltrion Inc. announced plans to acquire from Eli Lilly and Co. a Branchburg, N.J.-based biologics cGMP facility for $330 million up front, with plans to invest up to a total of ₩1.4 trillion (US$1 billion) in plant acquisition and expansion.
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Rexulti

CRL halts Otsuka’s drive for a PTSD treatment

Sep. 23, 2025
By Lee Landenberger
No Comments
The first new U.S. FDA-approved therapeutic option for PTSD in more than 20 years will have to wait. A supplemental NDA seeking approval of Rexulti (brexpiprazole) combined with sertraline, filed by one of Japan’s biggest pharmas, Otsuka Pharmaceutical Co. Ltd., received a complete response letter (CRL) from the agency.
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Handshake, money, calculator, MA-letters

Biotech leaders: Macroeconomics, US policy shifts making M&A harder

Sep. 23, 2025
By Nuala Moran
No Comments
The unsettling impact that the Trump administration’s health care and tariff initiatives are having on M&A activity and financing is highlighted in a new survey of CEOs and investors, who say uncertainty related to the U.S. policy environment is the top challenge they face when it comes to executing deals.
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Globe showing Asia-Pacific region
Asia Bio 2025

Piecing mosaic of APAC regulations key to Asia biotech growth

Sep. 16, 2025
By Marian (YoonJee) Chu
No Comments
“The comment I hear a lot from scientists … is that science has no borders,” Arif Noorani, partner at Sidley Austin LLP, said while addressing the panel audience at Asia Bio 2025 in Singapore. “I agree, but the reality is, we do have a lot of borders.”
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Deal illustration

Novartis taps Argo again, inks potential $5.2B collaboration

Sep. 9, 2025
By Jennifer Boggs
No Comments
Argo Biopharmaceutical Co. Ltd. and its RNAi work drew Novartis AG back to the table for a third time, as the companies entered a potential $5.2 billion deal involving cardiovascular-focused assets, including a right to first negotiation for BW-00112, an angiopoietin-like protein 3-targeting siRNA in phase II testing in severe hypertriglyceridemia.
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Dennis-Slamon speaks at GBC 25
Global Bio Conference 2025

The ‘molecular revolution’ driving R&D of new cancer therapeutics

Sep. 9, 2025
By Marian (YoonJee) Chu
No Comments
“New explosions in biotechnology are allowing us to interrogate cancers at a very sophisticated level compared to before,” Dennis Slamon told audience members at the Global Bio Conference in Seoul, South Korea Sept. 3.
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AI dollar sign

Propanc to acquire $100M of Ethereum to accelerate pipeline

Sep. 9, 2025
By Tamra Sami
No Comments
Propanc Biopharma, Inc. plans to acquire $100 million of Ethereum cryptocurrency over the next 12 months to accelerate its pipeline. The company is advancing its lead candidate, PRP, to enter a phase Ib trial in 30 to 40 advanced cancer patients with malignant solid tumors.
Read More
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