Genzyme and Boston Scientific Get Good News From the FDA; Acusphere and Targanta Not So Much; TransMedics Pulls IPO Plug; & More Boston-Area Life Sciences News

going to be more and more choosy about which firms and programs they support.

—Watertown, MA-based HIV drug developer Panacos Pharmaceuticals (NASDAQ:[[ticker:PANC]]) announced plans to reduce its staff from 33 workers to 15 and to explore such strategic options as a financing, partnership, sale of the company, or sale of certain assets.

—Ryan chatted with John Dunn, executive vice president of the VC arm of Biogen Idec (NASDAQ:[[ticker:BIIB]]). The Cambridge, MA-based firm this year committed an additional $100 million to Biogen Idec New Ventures; Dunn says he expects to invest the new allocation over a four-year period. Ryan also gave a quick overview of some of the 13 companies in the Biogen outfit’s portfolio.

An FDA panel recommended that biotech behemoth Amgen, which has operations in Seattle and Cambridge, MA, be required to run more clinical trials before it’s allowed to market its colorectal cancer drug, panitumumab (Vectibix), to patients with a specific genetic profile.

The FDA approved a new stent produced by Natick, MA-based Boston Scientific (NYSE:[[ticker:BSX]]). The device is designed to prop open renal arteries, which carry blood to the kidneys.

—Biogen Idec (NASDAQ: BIIB) announced that another patient taking natalizumab (Tysabri) has been diagnosed with PML, the rare and often fatal brain infection called PML.

—The quasi-public Massachusetts Life Sciences Center announced that Johnson & Johnson (NYSE:[[ticker:JNJ]]) will be the first member of a new consortium of firms that will provide matching funds to support Bay State life sciences startups and researchers. The agency also announced $3.7 million in grants to fund collaborative research between scientists and companies in the commonwealth, and plans to set up shop in 5,855 square feet of office space in Waltham.

—Andover, MA-based TransMedics, a developer of organ-transport systems, scrapped a planned IPO. The offering, originally announced in September of 2007, was to have been worth up to $86 million.

—Cambridge, MA-based Genzyme (NASDAQ: [[ticker:GENZ]]) won FDA approval for a drug designed to aid the treatment of patients with non-Hodgkin’s lymphoma and multiple myeloma. Plerixafor (Mozobil) is projected to generate about $75 million in sales in 2009.

Author: Rebecca Zacks

Rebecca is Xconomy's co-founder. She was previously the managing editor of Physician's First Watch, a daily e-newsletter from the publishers of New England Journal of Medicine. Before helping launch First Watch, she spent a decade covering innovation for Technology Review, Scientific American, and Discover Magazine's TV show. In 2005-2006 she was a Knight Science Journalism Fellow at MIT. Rebecca holds a bachelor's degree in biology from Brown University and a master's in science journalism from Boston University.