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BioWorld - Saturday, May 9, 2026
Home » Authors » Elise Mak

Elise Mak

Articles

ARTICLES

Illumina, Nky partner to develop genetic testing for kidney disease testing

March 14, 2019
By Elise Mak

Mgi unveils new advanced sequencing chemistry

March 13, 2019
By Elise Mak

Robot developer Hoz Medical closes series A funding round

March 12, 2019
By Elise Mak

Chinese regulators issue new rules after CRISPR scandal 'wake-up call'

March 6, 2019
By Elise Mak
HONG KONG – In the aftermath of last year's highly controversial case of a researcher announcing the birth of two gene-edited babies in China, the National Health Commission (NHC) released a set of draft regulations that increases scrutiny over the use of new high-risk biomedical technologies, such as gene editing, stem cell technology, cloning and assisted reproduction.
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China clears Betta to launch clinical testing of novel drug targeting FGFR-relevant tumors

March 6, 2019
By Elise Mak
HONG KONG – Hangzhou-based Chinese oncology drugmaker Betta Pharmaceuticals Co. Ltd. said Chinese regulators have given a green light for the company to conduct clinical trials for its novel compound, BPI-17509. Developed in-house, the oral small molecule is designed to selectively target fibroblast growth factor receptor (FGFR) 1, 2 and 3 to treat intrahepatic cholangiocarcinoma, bladder cancer and lung squamous cell carcinoma, among other FGFR-relevant solid tumors.
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China clears Betta to launch clinical testing of novel drug targeting FGFR-relevant tumors

March 5, 2019
By Elise Mak
HONG KONG – Hangzhou-based Chinese oncology drugmaker Betta Pharmaceuticals Co. Ltd. said Chinese regulators have given a green light for the company to conduct clinical trials for its novel compound, BPI-17509. Developed in-house, the oral small molecule is designed to selectively target fibroblast growth factor receptor (FGFR) 1, 2 and 3 to treat intrahepatic cholangiocarcinoma, bladder cancer and lung squamous cell carcinoma, among other FGFR-relevant solid tumors.
Read More

Chinese regulators issue new rules after CRISPR scandal 'wake-up call'

March 4, 2019
By Elise Mak
HONG KONG – In the aftermath of last year's highly controversial case of a researcher announcing the birth of two gene-edited babies in China, the National Health Commission (NHC) released a set of draft regulations that increases scrutiny over the use of new high-risk biomedical technologies, such as gene editing, stem cell technology, cloning and assisted reproduction.
Read More

With revised registration guidelines, China moves closer to harmonization

March 1, 2019
By Elise Mak

Henlius wins approval for China's first homegrown biosimilar

Feb. 27, 2019
By Elise Mak
HONG KONG – Chinese drug regulators have approved the first homegrown biosimilar, Shanghai Henlius Biotech Inc.'s HLX-01, a biosimilar referencing Roche Holding AG's Mabthera (rituximab), to treat non-Hodgkin lymphoma (NHL). It will be marketed as Hanlikang.
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Henlius wins approval for China's first homegrown biosimilar

Feb. 27, 2019
By Elise Mak
HONG KONG – Chinese drug regulators have approved the first homegrown biosimilar, Shanghai Henlius Biotech Inc.'s HLX-01, a biosimilar referencing Roche Holding AG's Mabthera (rituximab), to treat non-Hodgkin lymphoma (NHL). It will be marketed as Hanlikang.
Read More
View All Articles by Elise Mak

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