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BioWorld - Wednesday, May 6, 2026
Home » Authors » Marian (YoonJee) Chu

Articles by Marian (YoonJee) Chu

Woman and 3D brain

ABL lands £2B deal with GSK based on BBB passing drug platform

April 8, 2025
By Marian (YoonJee) Chu
ABL Bio Inc. announced April 7 that it sealed a potential £2.075 billion (US$2.65 billion) license deal with GSK plc, granting GSK global rights to use ABL’s blood-brain barrier (BBB) penetrating bispecific antibody platform, Grabody-B, to develop multiple programs in the neurodegenerative disease arena. Under the terms signed April 5, ABL agreed to transfer Grabody-B-related technology and know-how to GSK, upon which GSK will assume responsibility for preclinical and clinical development, manufacturing and commercialization.
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Sumitomo Pharma offloads two more subsidiaries

April 8, 2025
By Marian (YoonJee) Chu
Sumitomo Pharma Co. Ltd. announced that it will sell off two more of its subsidiaries, Sumitomo Pharma (China) Co. Ltd. and Sumitomo Pharma Asia Pacific Pte. Ltd. (and their subsidiaries), to Marubeni Global Pharma Corp. April 1, as the Japanese pharma continues restructuring efforts from last year.
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South Korea clears world’s first recombinant anthrax vaccine

April 8, 2025
By Marian (YoonJee) Chu
South Korea’s Ministry of Food and Drug Safety on April 8 cleared Barythrax injection (GC-1109) as the world’s first recombinant anthrax vaccine. The product was codeveloped by GC Biopharma Corp. and Korea Disease Control and Prevention Agency.
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Woman and 3D brain

ABL lands £2B deal with GSK based on BBB passing drug platform

April 7, 2025
By Marian (YoonJee) Chu
ABL Bio Inc. announced April 7 that it sealed a potential £2.075 billion (US$2.65 billion) license deal with GSK plc, granting GSK global rights to use ABL’s blood-brain barrier (BBB) penetrating bispecific antibody platform, Grabody-B, to develop multiple programs in the neurodegenerative disease arena. Under the terms signed April 5, ABL agreed to transfer Grabody-B-related technology and know-how to GSK, upon which GSK will assume responsibility for preclinical and clinical development, manufacturing and commercialization.
Read More
Radiopharma AMC

Radiopharmaceuticals stake more territory in breast cancer care

April 4, 2025
By Marian (YoonJee) Chu
Radiopharmaceuticals, including 16α-18F-fluoro-17β-estradiol (18F-FES) PET/CT, are emerging as powerful tools with new diagnostic and therapeutic potential in breast cancer diagnosis and treatment, Han Sang-won, professor from the department of nuclear medicine at Asan Medical Center, recently told BioWorld.
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Sumitomo Pharma offloads two more subsidiaries

April 3, 2025
By Marian (YoonJee) Chu
Sumitomo Pharma Co. Ltd. announced that it will sell off two more of its subsidiaries, Sumitomo Pharma (China) Co. Ltd. and Sumitomo Pharma Asia Pacific Pte. Ltd. (and their subsidiaries), to Marubeni Global Pharma Corp. April 1, as the Japanese pharma continues restructuring efforts from last year.
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GE Healthcare

GE Healthcare taps into Japan radiopharma market with Nihon buy

April 2, 2025
By Marian (YoonJee) Chu
GE Healthcare Technologies Inc. gained full ownership of Nihon Medi-Physics Co. Ltd. after acquiring the remaining 50% stake from Sumitomo Chemical Co. Ltd. on March 31.
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Daewoong researchers in the lab

Daewoong sees end of CS Pharma deal; new starts in cancer, DTx

April 1, 2025
By Marian (YoonJee) Chu
It was a mixed day for Daewoong Pharmaceutical Co. Ltd., which disclosed separately on March 28 both the termination of a $336 million licensing deal with CS Pharmaceuticals Ltd. and upbeat plans to unveil three new oncology assets at the upcoming American Association for Cancer Research in April.
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Daewoong researchers in the lab

Daewoong sees end of CS Pharma deal; new starts in cancer, DTx

March 28, 2025
By Marian (YoonJee) Chu
It was a mixed day for Daewoong Pharmaceutical Co. Ltd., which disclosed separately on March 28 both the termination of a $336 million licensing deal with CS Pharmaceuticals Ltd. and upbeat plans to unveil three new oncology assets at the upcoming American Association for Cancer Research in April.
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US FDA deals second blow to Hengrui-HLB’s liver cancer drug combo

March 25, 2025
By Marian (YoonJee) Chu
The U.S. FDA rejected, for the second time, Elevar Therapeutics Inc.’s NDA of a novel combination therapy for advanced liver cancer, which comprised Jiangsu Hengrui Pharmaceutical Co. Ltd.’s PD-1 inhibitor camrelizumab and HLB Co. Ltd.’s small-molecule tyrosine kinase inhibitor, rivoceranib.
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