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BioWorld - Saturday, January 24, 2026
Breaking News: BioWorld 2025 Year in ReviewBreaking News: BioWorld MedTech 2025 Year in ReviewBreaking News: Trump administration impacts continue to roil the life sciences sector
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Six months out, new EU rules still raising feasibility concerns

June 25, 2024
By Nuala Moran
The industry is again raising concerns that new EU health technology assessment rules coming into force on Jan. 12, 2025, will have the opposite of the desired effect and slow down access to innovative therapies.
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Novo CEO joins growing list of Rx execs bowing to HELP Committee

June 25, 2024
By Mari Serebrov
Novo Nordisk A/S’ CEO Lars Jørgensen is set to be the next executive in the U.S. Senate Health, Education, Labor and Pensions (HELP) Committee’s pharma parade of shame. HELP Chair Bernie Sanders (I-Vt.) announced June 24 that Jørgensen will testify before the committee Sept. 24 about his company’s U.S. pricing of its blockbuster semaglutide drugs, Ozempic and Wegovy.
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US FDA issues CRL for Abbvie’s Parkinson’s drug, ABBV-951

June 25, 2024
By Karen Carey
After receiving a complete response letter (CRL) in 2023 related to device issues, North Chicago-based Abbvie Inc. received another CRL for ABBV-951 (foscarbidopa/foslevodopa) for treating motor fluctuations in advanced Parkinson’s disease, this time for issues at a third-party manufacturer.
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mRNA on digital background
Newco news

Exsilio launches with $82M to develop mRNA-based gene therapies

June 25, 2024
By Brian Orelli
Exsilio Therapeutics emerged from stealth mode on June 25, 2024, with $82 million from a series A financing that was co-led by Novartis Venture Fund and Delos Capital. The company plans to use naturally occurring, mobile genetic elements to integrate therapeutic genes at a defined location in the genome, making it safer than random integration, which can cause tumor formation.
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No sweat: FDA approves Botanix’s axillary hyperhidrosis NDA

June 25, 2024
By Lee Landenberger
The U.S. FDA has approved the NDA for Sofdra (sofpironium) for treating excessive underarm sweating from Botanix Pharmaceuticals Ltd. The approval was based on two pivotal phase III studies and is approved for those ages 9 and older.
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Liver disease

Innovent’s mazdutide reduces liver fat content in obese patients

June 25, 2024
By Tamra Sami
Innovent Biologics Inc.’s glucagon-like peptide-1 receptor and glucagon receptor dual agonist, mazdutide, saw 80% reduction in liver fat content in patients with more than 10% liver fat content in the phase III Glory-1 obesity trial.
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Fosun Pharma to buy out Henlius in $691.7M merger deal

June 25, 2024
By Tamra Sami
Shanghai Fosun Pharmaceutical Co. Ltd announced it will buy out partner Shanghai Henlius Biotech Inc. for up to HKD$5.4 billion (US$691.7 million), according to a joint announcement on the Hong Kong Stock Exchange.
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IPO puzzle pieces

China’s Ascentage drafts confidential IPO for dual listing in US

June 25, 2024
By Marian (YoonJee) Chu
Suzhou, China-headquartered Ascentage Pharma Group Corp. Ltd. has filed plans for a confidential IPO to the U.S. SEC for a potential dual listing on both the U.S. and Hong Kong stock exchanges. News of the U.S. IPO came just a few days after Ascentage drew a $75 million equity investment from Osaka, Japan-headquartered Takeda Pharmaceutical Co. Ltd. with the issuance of about 24.3 million shares at a purchase price of HK$24.09 (US$3.08) per share.
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Regulatory actions for June 25, 2024

June 25, 2024
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Biogen, Biontech, BMS, Duality, GSK, Mimivax, Novavax, Oncoinvent, Roche, Sellas, Takeda, Valneva.
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Other news to note for June 25, 2024

June 25, 2024
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alimera, Amylyx, Ani, Effector, Eiger, Evommune, Progen, Rani.
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