GlaxoSmithKline Plc reported a rise in turnover of 13%, at constant exchange rates, in the first quarter, driven by sales of anti-viral and pandemic influenza products. Sales in western markets meanwhile contributed less to the total, than a year ago.
Novo Nordisk A/S said that modern insulins drove growth in the first quarter when sales, in local currencies, rose by 11% to DKK13.7 million (€1.84 million). At the end of the quarter, the Danish company claimed 51% of the global insulin market.
Cellular Dynamics International (CDI) Inc of Madison, Wisconsin has raised $40.6 million in a Series B private equity round to increase production capacity for its human heart cells derived from induced pluripotent stem cells (IPSCs).
MorphoSys AG has confirmed that it expects to report revenue of between €89 to €93 million in 2010, up from €81 million in 2009, and to report an operating profit of €5 to €9 million, compared with €11.4 million the previous year.
Companies looking to partner or licence a medical product or platform often have difficulty working out what the value is of what they are selling. If their product or platform is really new, there is no precedent for establishing value.
The European Medicines Agency’s main scientific committee has recommended that AstraZeneca’s Seroquel (quetiapine fumarate) be approved as an add-on to ongoing treatment for major depressive episodes in patients with major depressive disorder.
Supply shortages for the two Genzyme Corp enzyme replacement therapies, Cerezyme and Fabrazyme, are expected to continue until at least the end of September 2010 because of a new manufacturing problem, the European Medicines Agency said.
Positive EMA opinion for Nycomed’s Daxas. The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency has issued a positive opinion for the Nycomed GmbH medicine, Daxas (roflumilast) for the maintenance treatment of severe chronic obstructive pulmonary disease (COPD). The opinion was issued on 23 April, 2010. Roflumilast is an anti-inflammatory agent designed to target both the systemic and pulmonary inflammation associated with COPD. It does this by reducing the activity of phosphodiesterase 4 (PDE4), an enzyme found in body cells which is important to the pathogenesis of COPD. The review of the application started in 27 May 2009 and was under active assessment for 210 days. The benefits of the drug are its ability to reduce inflammation in the lungs, to reduce narrowing of airways and to ease breathing problems in adults with severe COPD, the agency said.
Two US centres of the Fraunhofer-Gesellschaft in Germany, together with Boston University and the biopharmaceutical company iBio, Inc, have launched a factory that uses non-genetically modified green plants to produce vaccines.
Novartis said that Zortress (everolimus) has been cleared by the US Food and Drug Administration to help adult patients with kidney transplants keep the transplanted organ. The drug is already approved as an immunosuppressant and a cancer drug.