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BioWorld - Friday, February 20, 2026
Home » Topics » Asia-Pacific, BioWorld Asia

Asia-Pacific, BioWorld Asia
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Prism offers Genentech peptide mimetic small-molecules library for multitarget collaboration

Jan. 11, 2022
By Gina Lee
Prism Biolab Co. Ltd. has added Genentech Inc., a unit of Roche Holding AG, to the list of users for its peptide mimetic small-molecules library after signing a multitarget research collaboration and licensing agreement.
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Kyowa Kirin expands Inveniai AI platform collaboration once again

Jan. 11, 2022
By Gina Lee
Inveniai LLC and Kyowa Kirin Co. Ltd. have expanded their partnership a second time, inking their most recent multiple drug discovery agreement. The multiyear deal will see the duo discover novel targets and treatments for therapeutic areas across Kyowa Kirin’s portfolio and areas of interest using Inveniai’s artificial intelligence (AI) platform.
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Wuxi Global Forum highlights need for computational technology, data to improve clinical trials

Jan. 11, 2022
By Doris Yu
Computational technology and high-quality data will help scientists to improve R&D and find better treatments for human diseases, according to experts at the Wuxi Global Forum 2022.
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RNA illustration

Sirnaomics starts 2022 with $64M Hong Kong IPO

Jan. 4, 2022
By Doris Yu
Sirnaomics Ltd. became the first RNA therapeutics company to list on the Hong Kong Stock Exchange (HKEX) with a $64 million initial public offering. Its shares (HKEX:2277) have since surged, rising to HK$93.90 ($12.04) on Jan. 4 following their debut at HK$65.90 per share.
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Australian flag on laptop screen with health professional

Australia is falling behind in accessing innovative drugs, devices

Jan. 4, 2022
By Tamra Sami
PERTH, Australia – Australia should be at the front of the line among developed nations when it comes to innovative drugs and devices, but health policies must evolve to respond to changes in technology and global trends, Johnson & Johnson (J&J) said. Although Australia’s health policy has served the country well, tensions in the system are becoming seismic shifts that mirror international trends, J&J said in a recent report on Australia’s health system.
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Flag of India

India seeking to improve domestic pharma and med-tech ecosystems with new guidelines

Jan. 4, 2022
By David Ho
India’s Department of Pharmaceuticals (DOD) released draft guidelines to boost research and development in its pharmaceutical and medical device industries. The document touched on the reasons for a dedicated R&D and innovation policy, which involved reducing import dependence, increasing the speed of biologic and biosimilar development cycles, and tackling infrastructural challenges.
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Antibodies attacking cancer cell

Legochem licenses out ADC to Iksuda in $1B deal

Dec. 28, 2021
By Gina Lee
Legochem Biosciences Inc. has licensed out its antibody-drug conjugate (ADC) LCB-14 to Iksuda Therapeutics Ltd. in the duo’s latest deal that is worth $1 billion. Daejeon, South Korea-based Legochem will receive $50 million in an up-front payment and near-term milestones, and up to $950 million in developments, regulatory and commercial milestones.
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Biosion licenses out anti-Trop2 humanized MAb to Obi Pharma

Dec. 21, 2021
By Doris Yu
Obi Pharma Inc. has acquired global rights to BSI-04702, an anti-trophoblast antigen 2 (Trop2) humanized monoclonal antibody (MAb), from Biosion Inc. Obi is granted exclusive rights for further preclinical and clinical development, registration and commercialization of the candidate as an antibody-drug conjugate and other derivative products.
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Providence and Everest’s vaccine is first mRNA in WHO’s Solidarity Trial Vaccines study

Dec. 21, 2021
By David Ho
Everest Medicines Ltd. and Providence Therapeutics Holdings Inc.’s COVID-19 vaccine was cleared for inclusion in the World Health Organization’s (WHO) Solidarity Trial Vaccines clinical trial.
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Handshake with digital globe overlay

Qilu in-licenses HBV-focused RNAi therapy from Arbutus in $300M deal

Dec. 21, 2021
By Doris Yu
Qilu Pharmaceutical Co. Ltd. licensed rights to AB-729, an RNA interference (RNAi) therapeutic from Arbutus Biopharma Corp., in a deal worth up to $300 million. Qilu obtained rights to develop and commercialize the phase II asset for the treatment of hepatitis B (HBV) in mainland China, Hong Kong, Macau, and Taiwan. Under terms of the agreement, Qilu will pay Arbutus $40 million up front, as well as up to $245 million in development, regulatory and sales milestones. In addition, Qilu will make a $15 million equity investment in Arbutus at a price of $4.19 per share.
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