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BioWorld - Monday, December 22, 2025
Home » Topics » Asia-Pacific, BioWorld

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Biomap signing ceremony

Biomap sets new global ‘biocomputing’ hub in Hong Kong

July 11, 2024
By Marian (YoonJee) Chu
Silicon Valley-based Biomap is setting up a new global biocomputing innovation hub, dubbed Biomap Innohub, in Hong Kong as the local government ramps up investment to build supercomputing prowess, Vicky Qu, senior vice president of Biomap, told BioWorld. The goal is to accelerate novel drug product development and commercialization with biocomputing.
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Brain scans

Kazia’s stock rockets on positive glioblastoma trial results

July 11, 2024
By Tamra Sami
Kazia Therapeutics Ltd.'s stock shot up 248% on July 10 after the Sydney-based company reported that paxalisib showed a 3.8-month improvement in overall survival, a 33% improvement, for newly diagnosed unmethylated patients with glioblastoma (GBM) compared to the concurrent standard-of-care arm in the pivotal GBM-Agile phase II/III study.
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Single strand RNA

BIX Korea 2024: Promise of mRNA technology for cell and gene therapy

July 10, 2024
By Marian (YoonJee) Chu
The industry is looking, with renewed hope, to the “promise” of messenger RNA (mRNA) therapeutics for a wide range of diseases beyond COVID-19, and not only in vaccine form but also for gene and cell therapies.
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Alteogen’s Altos nabs ₩24.5B in series B to develop new eye drug

July 9, 2024
By Marian (YoonJee) Chu
Altos Biologics Inc., founded as an eye disease-focused subsidiary of Alteogen Inc. in 2020, raised ₩24.5 billion (US$17.7 million) in a series B financing round to advance its pipeline of therapeutics for eye-related conditions, including age-related macular degeneration (AMD). Daejeon, South Korea-based Alteogen said July 9 that the funds raised will be funneled to develop OP-01, Altos’ candidate therapy for AMD.
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Kidneys

Biocity’s SC-0062 hits endpoint in chronic kidney disease trial

July 9, 2024
By Tamra Sami
Biocity Biopharmaceutics Co. Ltd.’s selective endothelin receptor type A antagonist, SC-0062, met the primary endpoint of reducing proteinuria in a phase II chronic kidney disease trial. The candidate showed a clinically meaningful and statistically significant reduction in proteinuria, with a clear dose-response relationship and good safety profile.
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Woman taking medication for mental illness
Newco news

Douglas gears up for slow-release ketamine phase III for depression

July 8, 2024
By Tamra Sami
On the heels of positive phase II results of its extended-release ketamine (R-107) in treatment-resistant depression, Douglas Pharmaceuticals Ltd. is gearing up to begin phase III trials of its ketamine treatment that is safe enough to take at home without clinical supervision.
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Iaso buys out Innovent’s rights to CAR T Fucaso

July 8, 2024
By Tamra Sami
Nanjing, China-based Iaso Biotherapeutics Co. Ltd. has bought out global rights to human anti-B cell maturation antigen CAR T Fucaso (equecabtagene autoleucel) from partner Innovent Biologics Inc.
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Deal illustration

Genexine, EPD Biotherapeutics to merge for new protein degraders

July 5, 2024
By Marian (YoonJee) Chu
Seoul, South Korea-based Genexine Co. Ltd. plans to merge with privately held EPD Biotherapeutics Co. Ltd. by October 2024 to build a pipeline of novel targeted protein degradation therapeutics with EPD Bio’s BioPROTAC platform technology.
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Lotte Biologics CEO Richard Lee

Lotte Biologics to build $3.3B South Korea biomanufacturing plant

July 3, 2024
By Marian (YoonJee) Chu
Lotte Biologics Co. Ltd. broke ground on its contract development and manufacturing organization (CDMO) plant at its Songdo Bio Campus in Incheon, South Korea, on July 3 to grow its production capacity and set “a new standard” for Korean CDMOs in the global market.
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Bar chart, downward arrow

Biosecure Act leaves biopharmas less confident in Chinese partners

July 3, 2024
By Tamra Sami
Confidence in working with Chinese biopharma companies has dropped by 30% to 50% for U.S.-based life sciences companies, with Chinese contract development and manufacturing organizations the hardest hit, according to a recent LEK survey of global life sciences companies on the impact of the pending U.S. Biosecure Act.
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