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BioWorld - Thursday, July 9, 2026
Home » Topics » Asia-Pacific, BioWorld

Asia-Pacific, BioWorld
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BioKorea 2022: As microbiome therapies emerge, leaders see challenges, opportunities

May 11, 2022
By Gina Lee
Microbiome-modulating therapies are increasingly being explored to treat a variety of diseases. However, the market is still in its infancy and a lack of solid regulations remains challenging for companies to overcome, speakers at the BioKorea 2022 said May 11.
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Juniper acquires infigratinib rights from Helsinn in emerging markets

May 6, 2022
By David Ho
Juniper Biologics Pte. Ltd. has added another candidate to its pipeline in the space of less than a month. In the latest deal, the Singapore-based company inked an exclusive licensing agreement with Switzerland’s Helsinn Healthcare SA, gaining rights to develop and commercialize oncology drug infigratinib in Australia, New Zealand, Southeast Asia and certain markets in the Middle East and Africa.
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Chinese flag on flagpole

China’s NMPA approves Pfizer’s third-generation ALK inhibitor Lorbrena in NSCLC

May 3, 2022
By Tamra Sami
China’s National Medical Products Administration (NMPA) gave the green light to Pfizer Inc.’s third-generation anaplastic lymphoma kinase (ALK) inhibitor, Lorbrena (lorlatinib), for patients with ALK-positive advanced non-small-cell lung cancer (NSCLC).
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Gold dollar sign inside gold cog
Newco news

Chimera going for ‘Gold’ as AFCR award boosts funding round

April 28, 2022
By David Ho
Chimera Bioengineering Inc. has been selected as the winner of the Asian Fund for Cancer Research's (AFCR) 2021 BRACE Award Venture Competition, contributing $500,000 as part of a recent $7.5 million capital infusion and bringing to $26 million the company’s total amount raised to date.
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Clinical research concept with medical icons on light bulb

With positive phase III Tibsovo data, Servier and Cstone targeting AML

April 26, 2022
By Doris Yu
Backed by fresh phase III data showing a combination of the IDH1 gene inhibitor Tibsovo (ivosidenib) and azacitidine significantly improved event-free survival and overall survival for adults with previously untreated IDH1-mutated acute myeloid leukemia (AML) vs. azacitidine alone, Cstone Pharmaceuticals Co. Ltd. is working to bring the treatment to Chinese AML patients “as soon as possible,” a spokesperson told BioWorld.
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Lungs

Bridge Biotherapeutics inks ₩30B deal with Shaperon for GPCR19 agonist

April 22, 2022
By Gina Lee
Bridge Biotherapeutics Inc. inked an exclusive in-license agreement for Shaperon Inc.’s G protein-coupled receptor 19 (GPCR19) agonist, BBT-209, a potential treatment for idiopathic pulmonary fibrosis. Bridge will pay Shaperon ₩2 billion (US$1.63 million) up front. The potential deal value, which includes up-front, milestone, and royalty payments, is ₩30 billion.
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SK Biopharmaceuticals and Ubix to develop cancer treatments using targeted protein degradation

April 21, 2022
By Gina Lee
South Korean companies Ubix Therapeutics Inc. and SK Biopharmaceuticals Co. Ltd. are partnering to develop targeted protein degradation cancer therapies.
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Genequantum collaborates with Aimedbio to develop ADC for brain tumors

April 20, 2022
By Doris Yu and Gina Lee
Genequantum Healthcare Co. Ltd. will work with Aimedbio Inc. to co-develop an antibody-drug conjugate (ADC) to treat brain and other cancers, working toward an IND filing in 2023.
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Knee pain illustration

Juniper Biologics acquires gene therapy for knee osteoarthritis in $600M deal from Kolon Life Science

April 14, 2022
By David Ho and Gina Lee
Through a $600 million deal, Juniper Biologics Pte. Ltd. has acquired rights from Kolon Life Science Inc. to develop and commercialize TG-C LD (Tissuegene-C low dose) for the treatment of knee osteoarthritis. Singapore-based Juniper will hold the rights for Asia Pacific, the Middle East and Africa and be responsible for developing and commercializing the candidate within those regions.
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Late-stage trial finds Celltrion’s bevacizumab biosimilar comparable to Avastin

April 14, 2022
By Gina Lee

Results from a phase III study comparing Celltrion Inc.’s biosimilar VEGF ligand inhibitor CT-P16 to Roche Holding AG’s Avastin (bevacizumab) in patients with metastatic or recurrent non-squamous non-small-cell lung cancer (NSCLC) found it to be similarly effective and as safe compared to the reference drug. Incheon, South Korea-based Celltrion presented the results at the 2022 annual meeting of the American Association for Cancer Research. The company now plans “to speed up the approval process through consultation with regulatory authorities in each country,” a Celltrion official said.


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