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BioWorld - Tuesday, December 30, 2025
Home » Newsletters » BioWorld Asia

BioWorld Asia

Nov. 25, 2025

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Red and blue bispecific antibodies

Phrontline raises $60M in pre-A+ round for bispecific ADCs

Phrontline Biopharma Suzhou Co. Ltd. closed a $60 million pre-A+ financing round led by Lapam Investment, with participation from nine other investors. The funds raised will support Phrontline’s development of next-generation antibody-drug conjugate (ADC) candidates. Read More

Otsuka submits NDA for new non-stimulant ADHD therapy

Otsuka Pharmaceutical Co. Ltd. filed an NDA with the U.S. FDA for centanafadine (formerly EB-1020), a new nonstimulant therapy for treating attention-deficit hyperactivity disorder (ADHD) in children, adolescents and adults. Centanafadine is a norepinephrine, dopamine and serotonin reuptake inhibito formulated as a once-daily extended-release capsule. Read More
Korean Won currency symbol made of gray cast iron

New Samyang Holdings, Samsung Biologics spin-offs debut on Kospi

Two South Korean conglomerates – Samyang Holdings Corp. and Samsung Biologics Co. Ltd. – listed their newly spun-off biopharmaceutical units on Korea Exchange’s (KRX) main trading board Nov. 24. Read More
Lymph nodes and lymphatic vessels

Protara sees Chugai blue sky in LMs as phase II data strong

Success in Japan may further bolster Protara Therapeutics Inc. in its push with TARA-002 in pediatric patients with macrocystic and mixed cystic lymphatic malformations (LMs), for which the New York-based firm disclosed interim results from an ongoing phase II trial. Read More
Doctors examining lung scans

Taiho, Cullinan file rolling NDA on phase I/II zipalertinib data

With phase I/II data in hand, Taiho Pharmaceutical Co. Ltd. and Cullinan Therapeutics Inc. began filing a rolling NDA to the U.S. FDA for accelerated approval of zipalertinib to treat patients with locally advanced or metastatic non-small-cell lung cancer with epidermal growth factor receptor exon 20 insertion mutations who previously received platinum-based chemotherapy. Read More
Acute myeloid leukemia

GSK, LTZ partner to develop myeloid cell engagers

Immunotherapy-focused biotech company LTZ Therapetics Inc. and GSK plc are partnering to develop up to four potential first-in-class myeloid cell engagers using LTZ’s immune-engager platform to target blood cancers and solid tumors. Read More

FDA investigating Takeda’s Adzynma after reports of death

The U.S. FDA said postmarketing reports of neutralizing antibodies to ADAMTS13, including one reported patient death, have prompted an investigation into Takeda Pharmaceutical Ltd.’s Adzynma (apadamtase alfa), a recombinant protein product approved in 2023 for use in adults and pediatric patients with congenital thrombotic thrombocytopenic purpura. Read More

Appointments and advancements for Nov. 24, 2025

New hires and promotions in the med-tech industry, including: BioCardia, Galvanize Therapeutics, Labcorp, Q Holdings. Read More

Financings for Nov. 25, 2025

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

In the clinic for Nov. 25, 2025

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Jyong Biotech, Lynk, Innovent. Read More

Other news to note for Nov. 25, 2025

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: Actimed, Aptose, Austrianova, Avant, Celltrion, Cytomed, Hanmi, Kazia, Klothea, Klothonova, Mankind Pharma, Microbiotix, Nxera, TC Biopharm, Trioar. Read More

Regulatory actions for Nov. 25, 2025

Regulatory snapshots, including drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations in Asia-Pacific: Celltrion, Henlius, Obi Pharma. Read More

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