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Home » Newsletters » BioWorld Asia

BioWorld Asia

June 5, 2013

View Archived Issues

Bergenbio's AXL-Kinase Inhibition Potential Is Broad

LONDON – Bergenbio AS has raised $6 million in a Series B round supported by all the existing investors, providing funding for a number of Phase I trials of its lead product BGB 324, a first-in-class AXL receptor tyrosine kinase inhibitor. Read More

Neuroblastoma Discovery May Lead to Wider Cancer Treatment

LONDON – A new study has given hope that it may one day be possible to develop a specific treatment for neuroblastoma, which is a rare type of childhood cancer. Read More

Biotech Flourishing in Flanders; Busy Hub a Standout in Europe

GHENT, Belgium – Patrik De Haes, CEO of Thrombogenics NV, rang the opening bell – albeit remotely – on the NYSE Euronext Brussels exchange to kick off proceedings at the 2013 Knowledge For Growth meeting at the International Convention Center in Ghent, Belgium, last Thursday. Read More

Oxagen Spinout Atopix to Advance Allergy Pipeline

LONDON – A new company has been spun out of genomics pioneer Oxagen Ltd. to take forward the lead compound OC459 in fresh indications. Read More

Nanobiotix Nanoparticle Targets Radiotherapy Effects on Tumors

LONDON – Nanobiotix SA presented positive safety data from the first clinical study of NBTXR3, a nanoparticle drug that enhances the effects of radiotherapy on tumor cells without damaging healthy tissue, at the American Society of Clinical Oncology (ASCO) meeting in Chicago on Saturday. Read More

Big Pharma Must Embrace Disruption or Get Run Over

GHENT, Belgium – The pharmaceutical industry has enjoyed 60 years of stability and is now – whether it likes it or not – ripe for disruption. That was the main message Bernard Munos, of InnoThink Center for Research in Biomedical Innovation in Indianapolis, delivered to delegates at a heavily attended keynote at the Knowledge for Growth meeting at the International Convention Center last week. Read More

Other News To Note

• Sinovac Biotech Ltd., of Beijing, said its new drug application for its EV71 vaccine was filed and accepted by the Beijing Drug Administration. Sinovac completed Phase III studies in March showing a 95 percent efficacy rate for the vaccine against hand, foot and mouth disease caused by enterovirus 71. Read More

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