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BioWorld - Tuesday, June 23, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

Sep. 2, 2025

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Spikevax vial and product packaging

South Korea clears Moderna’s Spikevax LP.8.1 vaccine for COVID-19

South Korea’s Ministry of Food and Drug Safety approved Moderna Inc.’s Spikevax LP.8.1 vaccine as an updated shot for COVID-19 targeting the LP.8.1 variant, according to Moderna Korea’s announcement Sept. 1. The regulatory clearance comes days after the U.S. FDA accepted, on Aug. 27, Moderna’s supplemental BLAs for two of its COVID-19 vaccines, Spikevax and Mnexspike. Read More
Financial chart and flag of China

Chinese biopharma financings up in Hong Kong

Financings are on the rise in Hong Kong as a number of Chinese pharmaceutical companies announced capital raisings, including Simcere Pharmaceutical Group Ltd., Qyuns Therapeutics Co., Ltd., Harbour Biomed Ltd. and Cutia Therapeutics. Read More
K-Sure Chairman and President Jang Young-jin Ryu (right) with KPTA Chairman Ryu Hyung-seon at the MOU signing

Korea pharma group to support exports, Korea-Japan-China trade

The Korea Pharmaceutical Traders Association said Aug. 26 that it signed a strategic agreement with Korea Trade Insurance Corp. to support South Korean companies exporting biopharmaceutical materials overseas. Read More

Fosun out-licenses immunology candidate to Sitala in $675M deal

Shanghai Fosun Pharmaceutical (Group) Co. Ltd.’s subsidiary, Shanghai Fosun Pharma Industrial, signed off ex-China rights to a phase II small-molecule inhibitor, FXS-6837, to Sitala Bio Ltd. in a potential $675 million deal. Read More
Kidney disease illustration

Vor and Remegen post another phase III win

The recombinant fusion protein drug telitacicept from Remegen Co. Ltd. and Vor Bio Inc. has notched a phase III win in treating adults with IgA nephropathy. The clinical trial of the fusion protein hit the primary endpoint, reducing proteinuria, too much protein in patients’ urine, in stage A of the study in China. Read More
Illustration of kidney cancer showing tumor inside the kidney

FDA issues CRL for Telix’s kidney cancer imaging agent

Telix Pharmaceuticals Ltd. received an FDA complete response letter (CRL) a day after the Aug. 27 PDUFA date for its BLA for radiopharmaceutical renal cancer imaging agent, Zircaix (TLX250-CDx, 89Zr-DFO-girentuximab). Read More
European flag, vial, syringe

Europe approves Bio-Thera’s Stelara biosimilar

Bio-Thera Solutions Inc. announced Aug. 26 that the European Commission cleared Usymro (BAT-2206) as a biosimilar to Janssen Pharmaceuticals Inc.’s Stelara (ustekinumab). The EMA issued marketing authorization for Usymro on Aug. 14, following the EMA’s Committee for Medicinal Products for Human Use adopting a positive opinion on June 19. Read More

Appointments and advancements for Sept. 2, 2025

New hires and promotions in biopharma in Asia-Pacific, including: Hutchmed. Read More

Financings for Sept. 2, 2025

Biopharmas in Asia-Pacific raising money in public or private financings: Aptose, Hanmi Pharmaceutical, Vaxxas. Read More

In the clinic for Sept. 2, 2025

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Akeso, Correctseqeuence Therapeutics. Read More

Other news to note for Sept. 2, 2025

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: Catalyst, Serb Pharmaceuticals. Read More

Regulatory actions for Sept. 2, 2025

Regulatory snapshots, including drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations in Asia-Pacific:Bio-Thera. Read More

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