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BioWorld - Saturday, July 18, 2026
Home » Topics » Regions » Asia-Pacific

Asia-Pacific
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Yunovia cleared for Korea phase I trial of small-molecule GLP-1 asset

Sep. 3, 2024
By Marian (YoonJee) Chu
Yunovia Co. Ltd. gained clearance in South Korea to start a multiple ascending dose phase I study for ID-110521156 – a novel, orally available, small-molecule, glucagon-like peptide-1 (GLP-1) agonist.
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Brain activity concept illustration

Despite clinical failure, new analysis supports Actinogen's Xanamem

Aug. 30, 2024
By Tamra Sami
After initially reporting that Xanamem failed to meet the primary endpoint in cognitive attention in the phase IIa Xanacidd cognition and depression trial, Actinogen Medical Ltd. CEO Steven Gourlay said a new analysis shows clinically and statistically significant benefits in depression.
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Gene editing illustration

Yoltech licenses gene editing therapy to Salubris for $145M

Aug. 29, 2024
By Tamra Sami
Yoltech Therapeutics Co. Ltd. licensed its PCSK9-targeting gene editing therapeutic, YOLT-101, to Shenzhen Salubris Pharmaceuticals Co. Ltd. for mainland China rights in a deal worth ¥1.035 billion (US$145 million).
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Yunovia cleared for Korea phase I trial of small-molecule GLP-1 asset

Aug. 28, 2024
By Marian (YoonJee) Chu
Yunovia Co. Ltd. gained clearance in South Korea to start a multiple ascending dose phase I study for ID-110521156 – a novel, orally available, small-molecule, glucagon-like peptide-1 (GLP-1) agonist.
Read More
Australia flag with microscope, test tubes

Pfizer urges Australia to establish clear vision for life sciences

Aug. 27, 2024
By Tamra Sami
Pfizer Inc. is calling on the Australian government to establish priorities for the life sciences sector to attract more investment into research, clinical trials and manufacturing in Australia. The new report recommends that the government issue a life sciences vision akin to the one issued by the U.K. in 2021 to make the country more competitive to attract investment.
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HKEX exterior

TYK Medicines raises $74M in HKEX IPO to launch EGFR inhibitor

Aug. 27, 2024
By Tamra Sami
TYK Medicines Inc. made a strong debut on the main board of the Hong Kong Stock Exchange (HKSE), raising HK$579 million (US$74.32 million) to commercialize its lead compound, EGFR inhibitor TY-9591, now in pivotal trials in patients with EGFR mutation-positive lung cancer.
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Global handshake silhouette

Huadong gets China rights to Imbiologics’ Oxtima program for ₩430B

Aug. 27, 2024
By Marian (YoonJee) Chu
Imbiologics Inc. scored a potential ₩430 billion (US$315.5 million) deal with China’s Hangzhou Zhongmei Huadong Pharmaceutical Co. Ltd. for Oxtima, an autoimmune disease program with two assets co-developed by Seoul, South Korea-based HK Inno.N Corp.
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Antibody-drug conjugate

Adcendo licenses Multitude’s phase I-ready ADC for $1B+

Aug. 27, 2024
By Tamra Sami
Adcendo ApS has inked a deal with Multitude Therapeutics Inc. and is licensing Multitude’s phase I-ready antibody-drug conjugate (ADC), ADCE-T02, which targets tissue factor. Under the deal, Copenhagen, Denmark-based Adcendo gains exclusive development and commercialization rights for the ADC globally, excluding greater China (mainland China, Hong Kong, Macao and Taiwan) where Multitude retains all rights.
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Chinese flag on flagpole

US lawmakers flag clinical trials with ties to China military

Aug. 27, 2024
By Mari Serebrov
Drug and device sponsors conducting clinical trials in China to support U.S. FDA approval may want to reconsider their choice of trial sites, as trials conducted at hospitals and clinics affiliated with China’s military or in the Xinjiang Uyghur Autonomous Region could be in for increased scrutiny.
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Seegene Novaplex MPXV OPXV Assay

Asia med-tech stocks rise as WHO moves to contain mpox outbreak

Aug. 27, 2024
By Marian (YoonJee) Chu
Shares of Chinese and South Korean med-tech companies continued to rise after the World Health Organization declared mpox a public health emergency of international concern Aug. 14 after recent outbreaks.
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