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BioWorld - Friday, May 1, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Chi-Med wins China approval for first in-house oncology drug

Jan. 5, 2021
By David Ho
HONG KONG – Hutchison China Meditech Ltd. (Chi-Med) earned approval from China’s National Medical Products Administration (NMPA) for Sulanda (surufatinib) for the treatment of non-pancreatic neuroendocrine tumors (NETs).
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IPO puzzle pieces

Terms are set in the new year’s first IPOs

Jan. 5, 2021
By Lee Landenberger
Following a record-shattering year, terms were set for the first two biotech IPOs of 2021 in deals that could generate up to $300 million. Cullinan Oncology LLC, of Cambridge, Mass., set terms Jan. 4 for raising about $150 million by pricing 8.3 million shares in the $17 to $19 range.
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Health professional touching screen, digital/medical icons

Hummingbird taps Tempus’ AI for clinical trial in rare NRG1 fusion patients

Dec. 22, 2020
By David Ho
HONG KONG – Hummingbird Bioscience Pte. Ltd. is collaborating with artificial intelligence (AI) company Tempus Labs Inc. to advance HMBD-001, a differentiated anti-HER3 neutralizing antibody developed using Hummingbird's Rational Antibody Discovery platform, into clinical trials in HER3-driven cancers.
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Lung cancer illustration

Junshi’s phase III for toripalimab in NSCLC hits primary endpoint at interim peek

Dec. 22, 2020
By David Ho
HONG KONG – Shanghai Junshi Biosciences Co. Ltd.’s toripalimab has reached its prespecified primary endpoint of progression-free survival at the interim analysis of a phase III study in non-small-cell lung cancer (NSCLC), as efforts to expand approval of the anti-PD-1 antibody into other cancer types are underway.
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Pharmaengine inks partnership with Sentinel Oncology for checkpoint kinase 1 inhibitor SOL-578

Dec. 15, 2020
By Gina Lee
HONG KONG – Pharmaengine Inc. has signed a collaboration and licensing deal with Sentinel Oncology Ltd. for SOL-578.
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Kintor shares rise on early peek at HCC drug combo data

Dec. 15, 2020
By Michael Fitzhugh
Kintor Pharmaceutical Ltd. said it's "actively initiating" multiregional phase II/III trials to test a combination of GT-90001 (ascrinvacumab) and Opdivo (nivolumab) for advanced hepatocellular carcinoma.
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Denovo closes $46M series D to advance PKC-beta inhibitor in phase III cancer studies

Dec. 15, 2020
By Elise Mak
BEIJING – Denovo Biopharma LLC closed a series D financing round to raise nearly ¥300 million (US$46 million), just six months after its $83.5 million series C round.
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HKEX exterior

Harbour debuts on HKEX with $221M IPO, eyes innovation through partnership

Dec. 15, 2020
By Elise Mak
Clinical-stage biopharma HBM Holdings Ltd. (also known as Harbour Biomed) debuted on the Hong Kong Stock Exchange on Dec. 10, raising HK$1.71 billion (US$220.7 million) to advance its autoimmune candidates to commercial launches in 2023.
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Breast cancer awareness
SABCS 2020

In reversal of fortune, efti shows OS promise for metastatic breast cancer

Dec. 15, 2020
By Anette Breindl
Australian biopharma Immutep Ltd. saw its stock price jump 165% Dec. 10, as the company reported that adding its eftilagimod alpha (IMP-321, “efti”) to paclitaxel resulted in what the company called a “promising and improving” trend toward increased overall survival in women with metastatic hormone receptor-driven breast cancer.
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Impact Therapeutics closes $50M series C+ to advance Wee-1 inhibitor and PARP inhibitor

Dec. 8, 2020
By Elise Mak
Chinese biopharma Impact Therapeutics Inc. of Nanjing raised $50 million in a series C+ round on Nov. 30, two years after its $30 million series C round. Impact’s CEO Jun Bao told BioWorld that the majority of the proceeds would be used to take several programs forward. The financing round also paved the way toward an IPO.
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