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BioWorld - Sunday, December 14, 2025
Home » Newsletters » BioWorld Asia

BioWorld Asia

May 21, 2024

View Archived Issues
eye-analysis.png

Biocon, Samsung win FDA nods for interchangeable Eylea biosimilars

The U.S. FDA approved the country’s first two interchangeable biosimilars, or copy products, of Regeneron Pharmaceuticals Inc./Bayer AG’s Eylea (aflibercept) on May 20, to treat four eye-related conditions. The FDA granted the approvals to U.S.- and India-based Johnson & Johnson Services Inc./Biocon Biologics Ltd.’s Yesafili (aflibercept-jbvf; M-710) and South Korea’s Samsung Bioepis Co. Ltd.’s Opuviz (aflibercept-yszy; SB-15). Read More

Théa returns rights to Curacle’s oral diabetic macular edema drug

Théa Open Innovation, a subsidiary of France’s Laboratoires Théa SAS, returned rights to South Korea’s Curacle Co. Ltd.’s CU-06, an oral diabetic macular edema drug candidate. Curacle posted positive top-line phase IIa data of CU-06 just three months prior. Read More
USTR seal

Usual players show up again in US trade report of bad actors

The U.S. Trade Representative (USTR) once again called out the usual cast of characters in this year’s Special 301 Report for not playing by the rules when it comes to protecting intellectual property. And once again, industry asked the USTR to go further by placing new players on the list. Read More
Cityscape, US flag and virtual lock

US Biosecure bill advancing through Congress, new tariffs imposed

Shaking up corporate and pipeline structure, San Diego-based cancer developer Erasca Inc. in-licensed two assets from China-based biopharmas in all-cash deals, while laying off 18% of its workforce, primarily in drug discovery. The flurry of announcements made on May 16, which included $160 million raised in private placement, showed that Erasca would scrap three existing pipeline assets – ERAS-007, ERAS-801 and ERAS-4 – and reshape development to a RAS-targeting franchise. Read More
Concept of business partnership

Erasca buys-in assets from two China biotechs, slashes workforce

Shaking up corporate and pipeline structure, San Diego-based cancer developer Erasca Inc. in-licensed two assets from China-based biopharmas in all-cash deals, while laying off 18% of its workforce, primarily in drug discovery. The flurry of announcements made on May 16, which included $160 million raised in private placement, showed that Erasca would scrap three existing pipeline assets – ERAS-007, ERAS-801 and ERAS-4 – and reshape development to a RAS-targeting franchise. Read More

Dong-A ST invests ₩25B in Ildong subsidiary, inks cancer deal

To strengthen its cancer pipeline, South Korea’s Dong-A ST Co. Ltd. made a strategic investment of ₩25 billion (US$18.45 million) in Seocho-gu, Seoul-based Idience Co. Ltd., a cancer-focused subsidiary of Ildong Pharmaceutical Co. Ltd. on May 20. Read More

FDA issues CRL on rivoceranib-camrelizumab combo in liver cancer

South Korea’s HLB Co. Ltd. saw its stock (KOSDAQ:028300) drop nearly 30% on May 17 as CEO Jin Yang-gon announced the U.S. FDA’s complete response letter (CRL) to its NDA seeking approval of its rivoceranib and camrelizumab (Airtuika, Jiangsu Hengrui Pharmaceutical Co. Ltd.) combo for liver cancer. Read More
Joshua Smiley, president and chief operating officer, Zai Lab

Zai Lab exec buys stock as Augtyro, Vyvgart SC advances in China

Zai Lab Ltd., of Shanghai and Cambridge, Mass., has been on a regulatory roll in China, gaining approval of Bristol Myers Squibb Co.’s Augtyro (repotrectinib) for lung cancer on May 12 and NMPA acceptance of subcutaneous Vyvgart‘s (efgartigimod alfa SC) supplemental BLA with priority review on May 14. Read More

Report leads to suspension of Ecohealth, NIH rebuke

Citing the need to protect the public interest, the U.S. Department of Health and Human Services ordered an immediate government-wide funding suspension May 15 of Ecohealth Alliance Inc. while formal debarment proceedings are pending against the New York-based nongovernmental organization. Read More
Cholesterol plaque in artery

CSPC Pharmaceutical’s JMT-202 cleared to enter clinic in China for hypertriglyceridemia

CSPC Pharmaceutical Group Ltd.’s anti-βKlotho monoclonal antibody drug JMT-202 has received clearance from China’s National Medical Products Administration (NMPA) to enter clinical trials to lower triglyceride levels in patients with hypertriglyceridemia. Read More
Gunsoo Kim, CEO, Curocell

Bio Korea 2024: Curocell CEO points to rise, fall of CAR T trends

As South Korea’s Curocell Inc. looks to develop the country’s first homegrown CAR T-cell therapy, CEO Gunsoo Kim highlighted rising and falling trends in the global CAR T development space at Bio Korea 2024. Read More

Appointments and advancements for May 21, 2024

New hires and promotions in the med-tech industry in Asia-Pacific, including: Haemalogix, Hutchmed, Sumitomo. Read More

Financings for May 21, 2024

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

In the clinic for May 21, 2024

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Hutchmed, Innocare, Immutep, Recce, Sumitomo. Read More

Other news to note for May 21, 2024

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: Erasca, Joyo, Medshine, Torii, Verrica. Read More

Regulatory actions for May 21, 2024

Regulatory snapshots, including drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations in Asia-Pacific: Aribio, Asieris, Brii, Drug Farm, Eisai, HLB, Mabwell, Ractigen, Sumitomo, Zai Lab. Read More

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