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J&J releases mixed psoriasis data

At week 12 of the study, patients receiving CNTO 1275 achieved at least 75% improvement in their psoriasis, as measured by the Psoriasis Area Severity Index (PASI 75),

Diosynth extends manufacturing deal with PDL

Diosynth Biotechnology is a company that offers contract cGMP manufacturing of biopharmaceuticals. Retavase is used in the treatment of acute myocardial infarction (AMI) in adults for the improvement

FDA accepts Anesiva pain drug for review

Acceptance for filing of a new drug application means that the FDA has found the company's submission to be sufficiently complete to review. The agency usually makes a

Bayer drug linked to increased death risk

According to the researchers the safety of Trayslol, also known as aprotinin, came under scrutiny in 2006 after an observational study reported that aprotinin use was associated with

Biogen cancer drug gets fast track status

Biogen has also initiated a registartion trial of lumiliximab. Lumiliximab is an anti-CD23 monoclonal antibody. CD23 is highly expressed on B-CLL cells. The trial will compare treatment with

ViroPharma says CMV drug gets orphan status

Orphan drug designation entitles ViroPharma to seven years of market exclusivity in the US. Other potential advantages include protocol assistance, the potential for priority review, tax credits, and

Vitamin D may cut cancer risk

The researchers believe that vitamin D could prevent up to half of the cases of breast cancer and two-thirds of the cases of colorectal cancer in the US.

Bioenvision applies for expanded Evoltra label

Evoltra is currently approved in Europe to treat pediatric patients with relapsed or refractory acute lymphoblastic leukemia and where there is no other treatment option anticipated to result