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BioWorld - Friday, May 8, 2026
Home » Authors » Elise Mak

Articles by Elise Mak

Miracogen expands ADC deal with Synaffix

Jan. 21, 2020
By Elise Mak and David Ho
HONG KONG – In less than a year, China-based Shanghai Miracogen Inc. has extended its partnership with Oss, the Netherlands based Synaffix BV for a second antibody-drug conjugate (ADCs) candidate. The new deal is similar to one signed last year in that it gives Miracogen nonexclusive rights to Synaffix’s Glycoconnect and Hydraspace ADC technologies for use in a second clinical candidate.
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Oncologie boosts pipeline with phase II-ready bispecific candidate in Mereo deal

Jan. 21, 2020
By Elise Mak
BEIJING – In a deal that adds another clinical-stage program to its pipeline, U.S.-China biotech Oncologie Inc. has picked up global rights to phase II-ready anti-DLL4/VEGF bispecific antibody navicixizumab from London-based Mereo Biopharma Group plc.
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Aum Biosciences partners with Cyclica for cancer therapies development

Jan. 21, 2020
By Jihyun Kim and Elise Mak
HONG KONG - Singapore-based biotech Aum Biosciences Pte. Ltd., and Toronto, Canada-based biotech Cyclica Inc. have agreed to work together to apply Cyclica’s drug discovery platform in Aum’s R&D programs for the discovery of potential new cancer therapies. Aum will deploy its drug R&D skills including a biomarker-driven approach while Cyclica will contribute its AI-augmented platforms, Ligand Design and Ligand Express.
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Chi-Med’s surufatinib phase III trial halted early after meeting primary endpoint in advanced pancreatic NET

Jan. 21, 2020
By Elise Mak
BEIJING – Hong Kong-headquartered Hutchison China Meditech Ltd.’s (Chi-Med) called an early stop to its phase III pivotal study of surufatinib in advanced pancreatic neuroendocrine tumors (NET) in China after it met the predefined primary endpoint of progression-free survival.
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Chinese flag, charts

China launches price war to reshuffle pharma industry; Bayer cuts prices by 90% to secure market

Jan. 21, 2020
By Elise Mak
China announced Jan. 17 which further pharmaceutical companies it will buy from under its centralized procurement program that seeks the lowest prices. The price war has forced foreign players to revalue the Chinese market and prompted Chinese players to come up with survival strategies under a policy that aims to consolidate the industry.
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China promotes real-world evidence in R&D and approval with new guidelines

Jan. 16, 2020
By Elise Mak
BEIJING – China has released guidelines to promote the use of real-world evidence (RWE) in drug development and reviews.
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Oncologie boosts pipeline with phase II-ready bispecific candidate in Mereo deal

Jan. 16, 2020
By Elise Mak
BEIJING – In a deal that adds another clinical-stage program to its pipeline, U.S.-China biotech Oncologie Inc. has picked up global rights to phase II-ready anti-DLL4/VEGF bispecific antibody navicixizumab from London-based Mereo Biopharma Group plc.
Read More

Miracogen expands ADC deal with Synaffix

Jan. 15, 2020
By David Ho and Elise Mak
HONG KONG – In less than a year, China-based Shanghai Miracogen Inc. has extended its partnership with Oss, the Netherlands based Synaffix BV for a second antibody-drug conjugate (ADCs) candidate. The new deal is similar to one signed last year in that it gives Miracogen nonexclusive rights to Synaffix’s Glycoconnect and Hydraspace ADC technologies for use in a second clinical candidate.
Read More

Innovent scores first IND for TIGIT antibody and explores PD-1/RNAi combination

Jan. 14, 2020
By Elise Mak
China-based Innovent Biologics Inc. will need to get on two new tasks this year: Preparing for the first clinical trial for an anti-TIGIT antibody in China and investigating the combination therapy of its Tyvyt (sintilimab) and Sirnaomics Inc.’s STP-705.
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Business pipeline illustration

Transcenta closes $100M series B+ to advance pipeline and IPO plan

Jan. 14, 2020
By Elise Mak
BEIJING – China-U.S. biotech Transcenta Holding Ltd., headquartered in Shanghai and  Boston, completed a series B+ financing round to secure $100 million to continue its efforts in developing oncology and bone disorder drugs and to prepare for an IPO.
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