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BioWorld - Thursday, January 15, 2026
Home » Authors » Marian (YoonJee) Chu

Marian (YoonJee) Chu

Articles

ARTICLES

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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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
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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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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Quantamatrix

Quantamatrix advances ultra-rapid uRAST test for sepsis

Aug. 23, 2024
By Marian (YoonJee) Chu
Quantamatrix Inc. is advancing an Ultra-Rapid Antimicrobial Susceptibility Testing sepsis diagnostic test, touted as having the world’s fastest all-in-one antimicrobial technology, to reduce sepsis diagnosis time from days to an average of 13 hours.
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Innovent wins nod for China’s first KRAS G12C lung cancer drug

Aug. 22, 2024
By Marian (YoonJee) Chu
The National Medical Products Administration (NMPA) has approved Innovent Biologics Inc.’s Dupert (fulzerasib) as the first KRAS G12C inhibitor in China to treat select patients with non-small-cell lung cancer (NSCLC).
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Lungs wireframe illustration

US FDA approves J&J’s Rybrevant-Lazcluze combo for lung cancer

Aug. 21, 2024
By Marian (YoonJee) Chu
The U.S. FDA approved Janssen Biotech Inc.’s Rybrevant (amivantamab-vmjw) plus a new oral tyrosine kinase inhibitor called Lazcluze (lazertinib) as a first-line combination treatment to treat select non-small-cell lung cancers.
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Global handshake silhouette

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

Aug. 20, 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.
Read More
Global handshake silhouette

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

Aug. 19, 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.
Read More

Cullinan ends $625M deal, returns Harbour’s cancer drug

Aug. 13, 2024
By Marian (YoonJee) Chu
Cullinan Therapeutics Inc. terminated development of Harbour Biomed Holdings Ltd.’s bispecific B7H4 x 4-1BB immune activator, CLN-418 (HBM-7008), after reviewing phase I data.
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View All Articles by Marian (YoonJee) Chu

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