News

Five medicines recommended for orphan designation in Europe

Five new investigational medicines have been recommended for designation as orphan medicinal products by a committee of the European Medicines Agency.  Producers of orphan-designated products may be eligible for grants and regulatory fee reductions.

UK Parliament backs hybrid embryo research

The UK House of Commons defeated opponents of a proposal to allow research using hybrid embryos. As a result, research involving hybrids will be allowed under a bill that updates the UK Human Fertilisation and Embryology Act 1990.

Ark Therapeutics gives business update

Ark Therapeutics Group Plc said that results of a corroborative Phase 3 study of its gene-therapy treatment for malignant glioma, Cerepro (sitimagene ceradenovec), should be available in the third quarter of 2008, paving the way for the filing of a marketing authorisation application for the product in Europe.

Biovitrum implements its strategic restructuring

Biovitrum, the Swedish pharmaceutical company, said on 15 May 2008 that it is implementing its strategic restructuring plan of November 2007. The plan involves licensing out or terminating most of its primary care products while bringing its niche products all the way to market

Allergy Therapeutics shares soar on Phase 3 trial results

Shares of Allergy Therapeutics Plc rose by more than 24% following the company’s announcement on 14 May 2008 that a Phase 3 trial of its hayfever vaccine, Pollinex Quattro, had met its primary efficacy endpoints. Allergy Therapeutics said it would apply for marketing approval in the European Union during first quarter of 2009.

MorphoSys increases net profit in 2008 first quarter

MorphoSys AG, the German biotechnology company, achieved a net profit of €3.3 million in the 2008 first quarter after €0.6 million a year earlier. The operating profit trebled to €4.1 million from €1.3 million on revenue of €16.3 million, against €14.1 million.