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BioWorld - Sunday, May 3, 2026
Home » Authors » Elise Mak

Articles by Elise Mak

Hansoh joins growing HKEX IPO queue, undeterred by volatility; China to follow?

Sep. 10, 2018
By Elise Mak and Alex Ho
HONG KONG – China-based Hansoh Pharmaceutical Group Co. Ltd. filed for an IPO in Hong Kong late last week, making it the 11th biopharma company to seek a listing on the Hong Kong Stock Exchange (HKEX) since May and following Ascentage Pharma Group International's IPO a week earlier.
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South Korea's JW Pharma out-licensed atopic dermatitis drug in $402M agreement

Sep. 6, 2018
By Elise Mak
HONG KONG – South Korea's JW Pharmaceutical Corp. out-licensed its atopic dermatitis candidate, JW-1601, to Danish medical dermatologist Leo Pharma A/S, which has rights to develop and commercialize the drug worldwide, except in South Korea.
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Ascentage follows Chinese biopharma peers to seek HKEX listing

Aug. 29, 2018
By Elise Mak
HONG KONG – The latest Chinese biopharma company to join the listing spree in Hong Kong was Suzhou-based Ascentage Pharma Group International, which last week filed its application to list on the Hong Kong Stock Exchange (HKEX).
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Roche gets CNDA nod for Alecensa for ALK-positive NSCLC

Aug. 29, 2018
By David Ho and Elise Mak
HONG KONG – Roche Holding AG was granted a rapid approval from the China National Drug Administration (CNDA) for Alecensa (alectinib). The drug was greenlighted as a monotherapy treatment for patients with anaplastic lymphoma kinase (ALK)-positive, advanced non-small-cell lung cancer (NSCLC).
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TLC reports positive phase II results for osteoarthritis pain therapy

Aug. 29, 2018
By Elise Mak
HONG KONG – Taiwan Liposome Co. Ltd. said its lead product candidate TLC-599, to treat osteoarthritis pain, has demonstrated promising results in its phase II study, making it a potential best-in-class intra-articular steroid for its duration of action.
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China approves Hengrui's HER2-positive breast cancer drug in 10 months

Aug. 28, 2018
By Elise Mak

HONG KONG – Jiangsu Hengrui Medicine Co. Ltd. said the China National Drug Administration (CNDA) granted a conditional approval to its self-developed compound pyrotinib for treating HER2-positive breast cancer. The approval was based on clinical data from phase II studies, demonstrating China's effort in marketing domestic innovative drugs faster.


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Roche gets CNDA nod for Alecensa for ALK-positive NSCLC

Aug. 28, 2018
By David Ho and Elise Mak
HONG KONG – Roche Holding AG was granted a rapid approval from the China National Drug Administration (CNDA) for Alecensa (alectinib). The drug was greenlighted as a monotherapy treatment for patients with anaplastic lymphoma kinase (ALK)-positive, advanced non-small-cell lung cancer (NSCLC).
Read More

TLC reports positive phase II results for osteoarthritis pain therapy

Aug. 27, 2018
By Elise Mak
HONG KONG – Taiwan Liposome Co. Ltd. said its lead product candidate TLC-599, to treat osteoarthritis pain, has demonstrated promising results in its phase II study, making it a potential best-in-class intra-articular steroid for its duration of action.
Read More

Ascentage follows Chinese biopharma peers to seek HKEX listing

Aug. 27, 2018
By Elise Mak
HONG KONG – The latest Chinese biopharma company to join the listing spree in Hong Kong was Suzhou-based Ascentage Pharma Group International, which last week filed its application to list on the Hong Kong Stock Exchange (HKEX).
Read More

Canbridge to start phase III trial for esophageal squamous cell cancer drug candidate

Aug. 22, 2018
By Elise Mak
HONG KONG – Canbridge Life Sciences Ltd., of Beijing, said it would soon initiate a phase Ib/III clinical study of its monoclonal antibody candidate CAN-017 in esophageal squamous cell cancer (ESCC). The multicenter study will evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of CAN-017 in combination with chemotherapy as the second-line treatment for patients with locally advanced or metastatic ESCC.
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