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BioWorld - Wednesday, March 4, 2026
Home » Authors » Elise Mak

Articles by Elise Mak

Suzhou biotech Connect adds $55M in series B financing for clinical trials in UC, Crohn's, AD

Jan. 7, 2019
By Elise Mak
HONG KONG – Chinese clinical-stage biotech Connect Biopharmaceuticals Ltd., of Suzhou, secured $55 million in a series B financing to move forward its two lead drug candidates, CBP-307 for treating ulcerative colitis and Crohn's disease and CBP-201 for treating atopic dermatitis, to the next stage.
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Antengene raises $120M in series B funding round

Jan. 4, 2019
By Elise Mak
HONG KONG - Chinese clinical-stage biotech Antengene Corp. raised $120 million in series B financing to move forward its lead programs, ATG-008 and ATG-010 (selinexor), for treating blood cancer and liver cancer, respectively.
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Second China-made PD-1 drug approved; Innovent's Tyvyt gets NMPA nod in HL

Jan. 2, 2019
By Elise Mak
HONG KONG – With Thursday's nod for Tyvyt (sintilimab injection), a core asset of HKEX-listed Innovent Biologics Inc. to treat classical Hodgkin lymphoma, either relapsed or refractory after two or more lines of systemic chemotherapy, Chinese regulators have approved two homegrown anti-PD-1 monoclonal antibodies in little more than a week.
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Taiwan startup Sinew aiming for first-in-class NASH drug

Jan. 2, 2019
By Elise Mak
TAIPEI, Taiwan – Taiwan startup Sinew Pharma Inc. is developing what it hopes will be a first-in-class drug to treat nonalcoholic steatohepatitis (NASH). With an investigational new drug (IND) approval by the U.S. FDA under its belt, Sinew plans to advance its core product to a phase IIb study next year.
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Taiwan startup Sinew aiming for first-in-class NASH drug

Jan. 2, 2019
By Elise Mak
TAIPEI, Taiwan – Taiwan startup Sinew Pharma Inc. is developing what it hopes will be a first-in-class drug to treat nonalcoholic steatohepatitis (NASH). With an investigational new drug (IND) approval by the U.S. FDA under its belt, Sinew plans to advance its core product to a phase IIb study next year.
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Second China-made PD-1 drug approved; Innovent's Tyvyt gets NMPA nod in HL

Dec. 31, 2018
By Elise Mak
HONG KONG – With Thursday's nod for Tyvyt (sintilimab injection), a core asset of HKEX-listed Innovent Biologics Inc. to treat classical Hodgkin lymphoma, either relapsed or refractory after two or more lines of systemic chemotherapy, Chinese regulators have approved two homegrown anti-PD-1 monoclonal antibodies in little more than a week.
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Jointo riding China's innovation push, baby boom to business success

Dec. 28, 2018
By Elise Mak

Approval boosts Junshi's trading debut on HKEX

Dec. 27, 2018
By Elise Mak
HONG KONG – Shanghai Junshi Biosciences Ltd. (HKG:1877) made a strong debut on the Hong Kong Stock Exchange, helped by China's first marketing approval of a homemade PD-1 monoclonal antibody last week. The biotech company's shares finished their first day of trading, on Dec. 24, up 22.55 percent to HK$23.75 (US$3.03).
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I-Mab licenses rights for diabetes treatment to CSPC for $21.7M

Dec. 26, 2018
By Elise Mak
HONG KONG – I-Mab Biopharma (Shanghai) Co. Ltd. out-licensed China rights to its long-acting glucagon-like peptide-1 (GLP-1) Fc protein, known as TG-103, to treat diabetes to CSPC Pharmaceutical Group Co. Ltd. for ¥150 million (US$21.7 million). As part of the deal, CSPC paid ¥15 million up front to I-Mab to obtain the exclusive license and will pay another ¥135 million based on the development progress of TG-103 in China as well as royalties.
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Approval boosts Junshi's trading debut on HKEX

Dec. 26, 2018
By Elise Mak
HONG KONG – Shanghai Junshi Biosciences Ltd. (HKG:1877) made a strong debut on the Hong Kong Stock Exchange, helped by China's first marketing approval of a homemade PD-1 monoclonal antibody last week. The biotech company's shares finished their first day of trading, on Dec. 24, up 22.55 percent to HK$23.75 (US$3.03).
Read More
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