Wilex AG’s lead cancer product – an antibody for renal cell carcinoma – has failed in a Phase 3 trial. The antibody, Rencarex (girentuximab), was already partnered and had been given fast track review status by the US Food and Drug Administration.
The non-profit drug developer, Aeras, has signed an agreement with GlaxoSmithKline Vaccines SA to advance the clinical development of a new vaccine against tuberculosis. A Phase 2b trial of the vaccine is scheduled to start in Kenya, India and South Africa.
Affimed Therapeutics AG of Germany has raised €15.5 million in venture capital to finance the early clinical testing of two bispecific antibody products developed to treat lymphomas. The Series D funding is being lead by existing investors.
ArGEN-X BV of the Netherlands has taken the unusual step of out-licensing its lead preclinical antibody compound to a Shanghai-based company which will take it into human studies in China and thereafter develop it.
Ablynx NV said that its antibody-fragment therapeutic, ALX-0061, has met the efficacy endpoint at week 12 in a Phase 1/2 trial of patients with rheumatoid arthritis. The compound targets the interleukin-6 receptor.
Ipsen SA’s haemophilia alliance with Inspiration Biopharmaceuticals Inc has come under strain following the US company’s failure to raise external financing. Ipsen announced on Wednesday that the ‘parties continue to explore various options.’
UCB SA said that a Phase 2b study of its candidate antibody for rheumatoid arthritis, olokizumab, met its primary endpoint. But there was no improvement in efficacy when the drug was compared with tocilizumab (Actemra).
Swedish Orphan Biovitrum (Sobi) has told analysts that its recombinant clotting factor product for haemophilia B achieved positive results in a Phase 3 trial, paving the way for a regulatory filing in the US in the first half of 2013.
Noxxon Pharma AG of Germany has started a Phase 2a study of an oligonucleotide-based drug in patients with multiple myeloma, a disease that accounts for about 1% of all cancers. The 28-patient, multi-center study is being conducted in Europe.
MorphoSys AG said its candidate antibody for rheumatoid arthritis targeting granulocyte macrophage-colony stimulating factor (GM-CSF) has shown an unusually high efficacy score at four weeks in a Phase 1b/2a clinical study.