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BioWorld - Monday, April 13, 2026
Home » Topics » Clinical, BioWorld Asia

Clinical, BioWorld Asia
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Innovent scores first IND for TIGIT antibody and explores PD-1/RNAi combination

Jan. 14, 2020
By Elise Mak
China-based Innovent Biologics Inc. will need to get on two new tasks this year: Preparing for the first clinical trial for an anti-TIGIT antibody in China and investigating the combination therapy of its Tyvyt (sintilimab) and Sirnaomics Inc.’s STP-705.
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Boy in wheelchair, scenic overlook

Australia’s Antisense Therapeutics’ phase II DMD trial meets primary endpoints for disease progression

Dec. 31, 2019
By Tamra Sami
PERTH, Australia – On the heels of a $1.15 billion deal between Roche Holding AG and Sarepta Therapeutics Inc. for Sarepta’s gene therapy to treat Duchenne muscular dystrophy (DMD), another therapy to treat DMD is emerging from Down Under.
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Liver disease

Boehringer Ingelheim quits development of Pharmaxis drug for NASH indication

Dec. 24, 2019
By Tamra Sami
PERTH, Australia – Boehringer Ingelheim GmbH is discontinuing development of BI-1467335 for the treatment of nonalcoholic steatohepatitis (NASH) that it acquired from Sydney-based Pharmaxis Ltd. in 2015.
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Cautious optimism for Biolinerx’s CXCR4 inhibitor in pancreatic cancer

Dec. 17, 2019
By David Ho
HONG KONG – Israel-based Biolinerx Ltd. has unveiled the latest data from its ongoing phase IIa COMBAT/KEYNOTE-202 study at the European Society of Medical Oncology Immuno-Oncology Congress 2019 which evaluates Biolinerx’s BL-8040.
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ESMO Asia 2019

Panelists urge better designs, more global focus for phase I trials

Nov. 26, 2019
By David Ho
SINGAPORE – While a lot of focus is placed on phase III trials and the subsequent approvals, panelists during the ESMO Asia Congress pointed to the importance of designing the right kind of phase I trials, from reaching global populations to using appropriate endpoints.
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ESMO Asia 2019

Quality of life and quality of studies take stage as Takeda reports solid NSCLC findings

Nov. 26, 2019
By David Ho
SINGAPORE – Takeda Pharmaceutical Co. Ltd. presented new findings from its phase III ALTA-1L trial evaluating its Alunbrig (brigatinib) vs. crizotinib in adults with advanced anaplastic lymphoma kinase-positive (ALK+) non-small-cell lung cancer (NSCLC) who had not received a prior ALK inhibitor, showing Alunbrig reduced the risk of disease progression or death by 76% after more than two years of follow-up.
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Hua Medicine achieves primary efficacy endpoint in phase III trial for type 2 diabetes candidate

Nov. 26, 2019
By David Ho
HONG KONG – China-based Hua Medicine (Shanghai) Ltd.’s phase III trial of a potentially first-in-class dual-acting glucokinase activator, dorzagliatin, met its primary efficacy endpoint.
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Aslan's varlitinib clinical study for BTC patients failed to meet primary endpoints

Nov. 19, 2019
By Jihyun Kim
HONG KONG – Singaporean drugmaker Aslan Pharmaceuticals Ltd. announced top-line data from its pivotal phase III TreeTopp (treatment opportunity with varlitinib (ASLAN-001) in biliary tract cancer) study in second-line biliary tract cancer patients, which failed to meet co-primary endpoints of progression-free survival (PFS) and overall response rate (ORR).
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Chinatrials12 Summit

With the help of trial experts, Chinese biotechs set sail for global market

Nov. 13, 2019
By Elise Mak
SHANGHAI – Innovation-driven biotech companies are sprouting up in China and they now aim to gain a bigger global presence through conducting clinical trials not just in their home country but also abroad.
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Visen to start phase III for China's first long-acting growth hormone for children

Oct. 30, 2019
By Elise Mak
BEIJING – Shanghai-based Visen Pharmaceuticals is pushing its long-acting growth hormone therapy, which is also the first of its kind in China, one step closer to the NDA-stage after receiving clearance from Chinese regulators this week to start a phase III trial.
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