News

Antibodies said to attack viruses within cells

Country
United Kingdom

Researchers funded by the UK Medical Research Council have reported that the human body has a system of intracellular immunity by which antibodies can fight viruses from within infected cells.

Gain in market share boosts Shire’s Q3 results

Country
United Kingdom

Shire Plc reported strong third quarter results, partly because it was able to nearly triple sales of two drugs that compete directly with products that Genzyme Corp is having trouble supplying.

GSK to invest $60 million in US orphan developer

Country
United Kingdom

GlaxoSmithKline Plc is to pay approximately $60 million upfront for a licensing agreement and equity investment in the US-listed biopharmaceutical company, Amicus Therapeutics Inc, which is developing a product for Fabry disease.

FDA turns down diabetes drug from Biodel

Country
United States

The US Food and Drug Administration has issued a ‘complete response letter’ to Biodel Inc of Danbury, Connecticut rejecting its new drug application for Linjeta, a rapid-acting injectable regular human insulin for Types 1 and 2 diabetes.

US researchers generate hepatic tissue

Country
United States

Researchers from the Institute for Regenerative Medicine at Wake Forest University’s Baptist Medical Center have seeded human liver cells in a laboratory and reportedly maintained them in a specialised bioreactor for up to one week.

FDA approves everolimus for benign brain tumour

Country
United States

The US Food and Drug Administration has approved the Novartis cancer drug, Afinitor (everolimus), for a new indication which is to treat patients with a benign brain tumour but who are not candidates for surgery.

MorphoSys increases proprietary R&D spending

Country
Germany

MorphoSys AG increased its proprietary research and development spending by 40% in the first nine months of 2010 – an indicator of the growing importance of its portfolio of internally-generated therapeutic antibodies.

FDA approves new indication for Sprycel

Country
United States

The US Food and Drug Administration has approved a new indication for the cancer drug, Sprycel (dasatinib), enabling it to be administered to patients with a rare blood cancer when it is first diagnosed.