Beacon NewsFlashes - February 7, 2011
Opinion: A Multiple Myeloma Patient’s Viewpoint On Randomized Clinical Trials – In the latest article published in the opinion section of The Myeloma Beacon, Dr. Jim Omel, a physician and multiple myeloma patient, wrote about how the clinical trial process could be changed to encourage greater participation among myeloma and other cancer patients. To receive a copy of all opinion articles when they are published or if you are interested in contributing an opinion piece, send an email to .
FDA Puts Carfilzomib On Fast Track For Treatment Of Multiple Myeloma – On January 31, Onyx Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) approved fast-track designation for carfilzomib, a second-generation proteasome inhibitor that has shown promising anti-myeloma activity as a single agent and in combination with Revlimid (lenalidomide) and low-dose dexamethasone (Decadron). The fast-track designation accelerates the review and approval process of drugs developed to treat serious or life-threatening illnesses. Onyx can now submit carfilzomib’s New Drug Application to the FDA on a rolling basis. For more information, please see the Onyx Pharmaceuticals press release.
Investigational Drug Siltuximab Enhances Melphalan Efficacy In Multiple Myeloma Cells – Pre-clinical results showed that the monoclonal antibody siltuximab (CNTO 328), which is being developed by Centocor Ortho Biotech, enhanced the activity of melphalan (Alkeran). Siltuximab increased melphalan’s toxicity to myeloma cells and neutralized interleukin-6, a protein that promotes growth and drug resistance of myeloma cells. Several clinical trials studying siltuximab in myeloma patients are ongoing. For more information, please see the study in the British Journal of Haematology (abstract).
Investigational Drug BI 2536 Is Active Against Multiple Myeloma Cells – Results from a recently published study show that BI 2536, which is being developed by Boehringer Ingelheim, induces cell death in multiple myeloma cells. BI 2536 inhibits an enzyme called polo-like kinase 1, which regulates the cell cycle and has been associated with the development of many cancers. Additionally, BI 2536 increased the efficacy of Velcade (bortezomib) and dexamethasone in these cell lines. The study authors concluded that the results suggest BI 2536 should be studied in clinical trials for multiple myeloma. For more information, please see the study in the journal Experimental Hematology (abstract).
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