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Home » Newsletters » BioWorld

BioWorld

March 12, 2014

View Archived Issues

Clinic roundup

Cytonet GmbH & Co. KG, of Weinheim, Germany, said interim data on its liver cell therapy treatment presented at the Society for Inherited Metabolic Disorders meeting in Pacific Grove, Calif., showed that pediatric patients with urea cycle disorders (UCDs) treated with the therapy had advantages in parameters such as event-free survival time or incidence of moderate or severe hyperammonemic events. Read More

Pharma: other news to note

Ventana Medical Systems Inc., of Tucson, Ariz., a member of the Roche Group, said it inked a multiyear deal with Bayer AG, of Leverkusen, Germany, to develop companion diagnostics, with a focus on immunohistochemistry, across Bayer’s portfolio of targeted therapy projects. Read More

Other news to note

Ambry Genetics Inc., of Aliso Viejo, Calif., defended itself against the preliminary injunction motion filed on July 9, 2013, by Myriad Genetics Inc., of Salt Lake City, and other plaintiffs in University of Utah Research Foundation et al. v. Ambry Genetics Corp. Read More

Financings roundup

Marina Biotech Inc., of Boston, closed its issuance of series C convertible preferred stock and common stock purchase warrants for gross proceeds of $6 million. Read More

Stock movers

Read More

Regulatory roundup

The EMA published the first summary for the public of the risk-management plan (RMP) of a newly authorized drug. The summary describes what is known and not known about the safety of Mumbai, India-based Piramal Imaging SA’s Neuraceq (florbetaben) and what measures will be taken to prevent or minimize the risks of the radiopharmaceutical used in brain scans. Read More

China’s new simplified M&A rules a step in the right direction

SHANGHAI – After a year of revisions, China’s Ministry of Commerce (MOFCOM) revealed its anticipated new “simple rules” for mergers and acquisitions. The move signals the government’s intentions toward fast-tracking deals that don’t trigger competition issues, but with the caveat that certain conditions apply. Read More

CMS backs away from proposed changes to Part D

Racing ahead of Congress, the Centers for Medicare & Medicaid Services (CMS) withdrew parts of a controversial rule revising the Medicare Part D prescription drug program. Read More

No chin-scratcher: Kythera takes back global ATX-101 rights from Bayer

Five months after an upsized follow-on offering brought in $120 million and in the midst of preparing its new drug application (NDA) to the FDA for ATX-101, Kythera Biopharmaceuticals Inc. pulled off a crafty reacquisition of global rights for the aesthetic candidate from Bayer Healthcare’s Consumer Care Division, a unit of Bayer AG, of Leverkusen, Germany. Read More

Still ‘galectin’ CKD data, La Jolla considers oral form; shares roar on phase II top-line

The higher-dose glitch in otherwise strong phase II results with its galectin-3-targeting chronic kidney disease (CKD) therapy did little to hold back shares of La Jolla Pharmaceutical Co. (NASDAQ:LJPC), which closed Tuesday at $17.96, up $7.06, or 64.8 percent. Read More

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