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BioWorld - Monday, July 20, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Singapore’s Tessa gains U.S. RMAT designation for CD30 CAR T, expands manufacturing efforts

March 3, 2020
By David Ho
HONG KONG – Tessa Therapeutics Pte Ltd.’s CD30 CAR T-cell therapy has been granted a regenerative medicine advanced therapy designation by the U.S. FDA based on data from two independent phase I/II trials.
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Shanghai, China, stock market illustration

Bio-Thera launches $241M pre-revenue IPO on Shanghai’s STAR; shares up 83% on debut

Feb. 25, 2020
By Elise Mak
BEIJING – Chinese biosimilar maker Bio-Thera Solutions Ltd., of Guangzhou, on Feb. 21 launched a pre-revenue listing on Shanghai’s STAR market to reap $241 million at a valuation of almost $2 billion.
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HKEX building

Akeso refiles IPO with HKEX amid coronavirus outbreak

Feb. 11, 2020
By Elise Mak
BEIJING – Zhongshan-based Akeso Inc., which focuses on bispecific antibodies, is again seeking pre-revenue listing on the Hong Kong Stock Exchange (HKEX), after its first IPO attempt failed to go through in December. The move comes at a time when analysts believe the coronavirus outbreak is weighing on the city’s IPO market. The second application, submitted on Feb. 3, was again supported by Morgan Stanley and J.P. Morgan. The clinical-stage biotech is reportedly seeking $300 million to support its R&D through the IPO, particularly its core asset, AK-104, a PD-1/CTLA4 bispecific antibody.
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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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South Korean won

Bionetix secures $9.33M in series B funding for AML/MDS and glaucoma treatment

Jan. 21, 2020
By Jihyun Kim
HONG KONG – Bionetix Inc., of Suwon, South Korea, has secured ₩10.8 billion (US$9.33 million) in series B funding. The biotech, founded in February 2017, has attracted a total of KRW14.7 billion to date. The company will use the funds to advance NTX-301, a therapy for myelodysplastic syndrome/acute myeloid leukemia (MDS/AML) with epigenetic dysregulation, and NTX-101, a glaucoma treatment.
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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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IPO, coins, financial chart

China’s I-Mab goes public in targeted range for $103.7M; after-market deep Zai?

Jan. 21, 2020
By Randy Osborne
Shanghai-based I-Mab Biopharma Co. Ltd. became the first IPO out of the gate this year, pricing its IPO of about 7.4 million American depositary shares (ADSs) – each 10 representing 23 ordinary shares of the company, par value $0.0001 per share – at $14 each, within the planned range of $12 at the low end and $15 at the high. But the stock’s performance might not have been all investors hoped, as shares (NASDAQ:IMAB) closed at $12.50 Jan. 17.
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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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KRAS protein

Targovax scores potential $100M KRAS vaccine deal in China

Jan. 14, 2020
By Cormac Sheridan
DUBLIN – Shares in Targovax ASA rose as much as 26% last Wednesday on news of an option and license agreement in China involving its peptide-based KRAS-directed cancer vaccines, TG-01 and TG-02.
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