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BioWorld - Wednesday, July 15, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

Feb. 20, 2013

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Approvals on the Rise, Though Translational Work Still Key

BOSTON – The rise in the number of new drug approvals granted by the FDA in the past three years looks encouraging – hinting as it does that the industry is putting the productivity woes of the previous decade behind it. Read More

Phenotypic Screening Making A Comeback, Scientists Say

BOSTON – Recent advances in the tools and technology for drug discovery mean it now takes minutes and days to accomplish tasks that previously took months and weeks. Read More

Biosimilar MAbs Starting to Line Up for Approval

LONDON – 2013 will be a watershed year for biosimilars – biological therapies designed to be similar to existing biological therapeutic agents – delegates attending the Second Biosimilars Congregation in London heard Tuesday. Read More

Diamyd Staves Off Liquidation, Returns Cash to Shareholders

Following pressure from a group of dissident shareholders, Diamyd Medical AB agreed to return most of its cash to its investors, while retaining a small amount to continue two Phase II trials of its GAD vaccine for the treatment and prevention of Type I diabetes. Read More

FDA Accepts Zealand's GLP-1 Drug Lixisenatide for Review

The FDA accepted for review a new drug application for lixisenatide, the once-daily glucagon-like peptide-1 (GLP-1) receptor agonist Zealand Pharma A/S has developed in partnership with Sanofi SA, paving the way for a possible U.S. approval in Type II diabetes by early 2014. Read More

Gene Location Affects Properties, Impacts on Regulatory Pathways

BOSTON – Location, location, location: The idea that one gene equals one protein is long discredited and research into mechanisms including post-translational modification of proteins and the baroque complexities of epigenetic control is advancing understanding of how one gene can generate multiple proteins. Read More

Other News To Note

• Dompe Group, of Milan, Italy, said the first patient has been enrolled in a Phase I/II REPARO study evaluating the ophthalmological use of a topical solution of recombinant human nerve growth factor (rhNGF) for the treatment of moderate to severe neurotrophic keratitis (NK). Read More

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