Sanofi Pasteur has become the second European company in a month to invest in antibody technology in order to discover new treatments for infectious diseases. It is paying €3 million upfront to Vivalis of France for access to the technology.
The French privately-owned immune therapy company, Cytheris SA, has raised €12 million in a Series D financing to accelerate development of its recombinant human interleukin-7 product, CYT107, for cancer and other indications.
Koninklijke Philips Electronics NV of the Netherlands has signed an agreement with the US discovery-stage company, RXi Pharmaceuticals, to explore the use of ultrasound for the delivery RNA interference compounds in cells.
A team of researchers in the US has reported that the CD95 receptor promotes tumour growth, a finding that advances work done at the German Cancer Research Center in Heidelberg, and at its spin-out, Apogenix GmbH.
Imperial Innovations Group Plc, a UK technology transfer company, said that it has realised £9.5 million in cash following the sale of its portfolio company, Respivert Ltd, to the Johnson & Johnson subsidiary, Centocor Ortho Biotech Inc.
Sanofi-Aventis said that it has reached an agreement to set up a joint venture in Japan with Nichi-Iko Pharmaceutical Co Ltd to develop genetic medicines. Sanofi will have a controlling interest in the venture to be called Sanofi-Aventis Nichi-Iko KK.
AstraZeneca Plc said its treatment for metastatic colorectal cancer, Recentin (cediranib), showed no improvement in overall survival in a Phase 3 trial, the second of two pivotal studies for this indication. A regulatory filing will not be made.
Noxxon Pharma AG said that it has raised €33 million in a Series D round of financing to support the ongoing clinical and preclinical development of its mirror-image oligonucleotides known as Spiegelmers. The round was led by NGN Capital.
The Novartis Group said that a Phase 3 trial of a drug for ovarian cancer failed to meet its primary endpoint and will not be submitted to the regulatory authorities. The drug, EPO906 (patupilone), did not show a significant overall survival advantage.
The European Medicines Agency has given its backing to data generated by a company which is developing a new cell therapy. It is the first time the regulator has formerly certified early-stage data for an advanced therapy product.