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BioWorld - Tuesday, December 23, 2025
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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IPO, coins, financial chart

Abbisko raises $226M in Hong Kong IPO to develop new solid tumor treatment

Oct. 19, 2021
By Doris Yu
Abbisko Cayman Ltd. has raised $226 million through an IPO in Hong Kong, where it launched with an initial price of HK$12.46 (US$1.60) per share. The company, doing business as Abbisko Therapeutics, plans to use about a third of the proceeds for research and development of its lead candidate, ABSK-091, as a potential treatment for multiple solid tumors.
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Antibody-drug conjugate

Third ADC candidate with Synaffix’s tech enters clinic as Miracogen kicks off phase I

Oct. 12, 2021
By David Ho
It looks like Shanghai Miracogen Inc.’s antibody-drug conjugate (ADC) partnership with Synaffix BV is paying off as MRG-004A, an ADC designed to treat solid tumors, has entered a U.S. phase I/II trial to treat solid tumors.
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CBMG’s facility in Shanghai

CBMG bags $120M in its first financing since going private, funds to benefit CAR T candidates

Oct. 5, 2021
By Gina Lee
Cell therapy developer Cellular Biomedicine Group Inc. (CBMG) completed a $120 million series A financing, its first since becoming a private company. The funds will benefit the U.S. and China-based firm’s CAR T pipeline.
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Padcev vial

Astellas and Seagen win Japanese approval for Padcev in advanced urothelial cancer

Sep. 28, 2021
By David Ho
Astellas Pharma Inc. and Seagen Inc. received approval through a priority review from Japan's Ministry of Health, Labour and Welfare for Padcev (enfortumab vedotin) to treat radically unresectable urothelial carcinoma that has progressed after chemotherapy. The green light for the antibody-drug conjugate is based on the global phase III EV-301 clinical trial, which included sites in Japan.
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Lung cancer illustration

Cstone presents positive phase III data of sugemalimab for NSCLC

Sep. 28, 2021
By Doris Yu
Cstone Pharmaceuticals Co. Ltd. released positive data from the phase III trial, Gemstone-302, of sugemalimab plus chemotherapy for the first-line treatment of patients with stage IV squamous and non-squamous non-small cell lung cancer.
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Illustration of cancer cells and immunotherapy treatment

HER2/neu space bustling, Greenwich duet shows promise

Sep. 28, 2021
By Randy Osborne
Imugene Ltd.’s recent win with a patent granted in Japan with its HER-Vaxx immunotherapy, in development for HER2-positive gastric cancer, represented a smallish but significant win in the HER2/neu space, where plenty of other players are busy, with Greenwich Life Sciences Inc. a strong emerging name.
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Beyondspring NSCLC phase III hits primary endpoint but stock sags anyway

Sep. 21, 2021
By Lee Landenberger
Despite Beyondspring Pharmaceuticals Inc.’s phase III study meeting its primary and key secondary endpoints of a plinabulin/docetaxel combination in treating non-small-cell lung cancer (NSCLC), the company stock (NADAQ:BYSI) took a pounding. Shares sunk 32.9% on Sept. 20 to close at $15.36 each.
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FDA Approved stamp with pills

FDA approves Takeda’s Exkivity for rare form of lung cancer

Sep. 21, 2021
By Richard Staines
Takeda Pharmaceutical Co. Ltd. has grabbed a slice of the non-small-cell lung cancer (NSCLC) market, becoming the first company to gain FDA approval for an oral drug targeted against a rare form of the disease.
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FDA accepts Beigene’s first filing outside China; BLA seeks nod for anti-PD-1 tislelizumab

Sep. 21, 2021
By Doris Yu
The FDA has accepted for review Novartis AG and Beigene Ltd.’s BLA filing for the anti-PD-1 monoclonal antibody tislelizumab.
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South Korean won

Abion shares drop in South Korean debut, but listing raises $33M for cancer therapies

Sep. 14, 2021
By Gina Lee
Abion Inc., which focuses on precision oncology, raised ₩38.76 billion (US$33.36 million) in its debut on the Korean Stock Exchange’s Kosdaq board on Sept. 8.
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