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BioWorld - Wednesday, January 14, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

Aug. 26, 2025

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Illustration of the spine with ankylosing spondylitis

Akeso’s gumokimab, manfidokimab meet phase III endpoints

Akeso Pharmaceuticals Inc.’s gumokimab (AK-111) and manfidokimab met all primary efficacy endpoints in its phase III trials in active ankylosing spondylitis and in moderate to severe atopic dermatitis, respectively. Read More
Imdelltra vials and product packaging

Beone sells off Amgen Imdelltra royalties for $950M

Beone Medicines Ltd. (formerly Beigene Ltd.) is selling its worldwide royalty rights on Imdelltra (tarlatamab) sales, excluding China, to Royalty Pharma for up to $950 million. Read More
Child feet

Ribomic’s RBM-007 ready for phase III in achondroplasia

Ribomic’s umedaptanib pegol (RBM-007) looks to have some advantages compared to competitors in the achondroplasia space, and the company plans to progress the oligonucleotide-based aptamer that targets anti fibroblast growth factor 2 to phase III trials, Ribomic’s business development head, Kihei Yamashita, told BioWorld. Read More

Remegen licenses VEGF/FGF inhibitor to Santen for ¥1.3B

Remegen Co. Ltd. is out-licensing its VEGF/FGF dual-target fusion protein drug, RC28-E, to Santen Pharmaceutical (China) Co. Ltd. in a carve-out deal worth more than ¥1.3 billion (US$180 million). Read More
K-Organoid Consortium

South Korea forms new organoid consortium for nonanimal testing

South Korea’s Ministry of Food and Drug Safety (MFDS) launched a new industry-academia-research consortium to support the nation’s organoid industry, expected to grow in light of the U.S. FDA’s shift away from animal testing in the development of novel drugs. Read More

Opthea avoids bankruptcy under new investor settlement

After announcing in April that it would discontinue development of its lead candidate, sozinibercept (OPT-302), in wet age-related macular degeneration (AMD), Opthea Ltd. has come to a settlement agreement that will allow it to avoid bankruptcy and continue operations. Read More

US FDA approves six NMEs in July; Kalvista, PTC, Regeneron rise

The U.S. FDA approved 17 drugs in July, down from 23 in June, bringing the year-to-date total to 125. Through July, 2025 remains the third-highest count in BioWorld’s records, trailing 135 approvals in 2024 and 126 in 2020. Read More

In the clinic for August 26, 2025

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Biomx, Enlivex, Kelun-Biotech. Read More

Other news to note for August 26, 2025

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: ARC Therapies, Bio-Thera, Dong-A, Kukbo, Redhill Biopharma, Roche, Stada Arzneimittel, Xtalpi. Read More

Regulatory actions for August 26, 2025

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

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