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A week in Seattle's life sciences land

It was not a good week to take time off. There was quite a bit of news. Here's a review, which I've arranged roughly in order of importance:

On the medical device front:

  • Physio-Control said it has reached an agreement with the FDA, under which it should eventually be able to start selling its defibrillators again. In January 2007, the Bothell-based unit of Medtronic voluntarily suspended shipments of its defibrillators, citing quality-control issues.

    The agreement appears to signal another delay in getting the defibrillators back on the market. We reported in November that the company was on track to resume full shipments by April 30 (read the story here).

    And on the biotech front:

  • Cell Therapeutics said it would raise roughly $28 million by selling preferred stock and debt to an institutional investor. The new funds were crucial since the company had $10.8 million in debt due in June and was short on cash. In a press release (read it here), Cell Therapeutics said that in addition to retiring the June debt, the company would use the new funds to purchase access to late-stage data of its Zevalin therapy, which it could potentially use to expand the cancer treatment's uses.

  • Genentech said its Rituxan treatment failed to meet the company's goals in a study looking at Rituxan's potential use in patients with lupus. Currently, the treatment is approved for patients with non-Hodgkin's lymphoma and rheumatoid arthritis. Kevin DeGeeter, an analyst at Oppenheimer & Co. and a noted bear on ZymoGenetics, wrote in a research report that "we view the data as a significant negative for (ZymoGenetics)." That's because, he argues, ZymoGenetics' Atacicept therapy has a "similar mechanism for B-cell suppression as Rituxan." ZymoGenetics is testing Atacicept in patients with lupus.

    On the topic of Atacicept, ZymoGenetics said Wednesday that partner Merck Serono had initiated a phase two trial of the treatment in patients with relapsing multiple sclerosis. (Read a release here.)

  • MediQuest Therapeutics said it had formally asked the FDA to approve its therapy for Raynaud's Disease, which the company calls MQX-503 (read our story on the announcement here). MQX-503 is a topical formulation which is designed to prevent or treat symptoms, including severe pain, associated with Raynaud's. Raynaud's disease affects mostly women and restricts blood flow to the fingers and toes, causing them to turn white. After the attack dies down, blood rushes back, creating red, tingly digits. More than 2 million people in the U.S. seek treatment each year for the disease, and MediQuest has said that it expects the market for its new drug to be worth more than $700 million.

  • Targeted Genetics said that an early-stage study of a gene therapy in three patients with Leber's congenital amaurosis showed that the therapy improved visual function in one of the patients. Leber's congenital amaurosis is a rare disease that results in total blindness by mid-age. There is no treatment. Targeted Genetics expects to enroll more patients in the study. Read Targeted Genetics' release here.

  • Acucela Inc. reported pre-clinical data, showing that animal models had demonstrated that a compound developed by the company had resulted in an "improvement in retinal abnormalities" in a blinding eye disease called retinopathy of prematurity. The company said the results were promising because in retinopathy of prematurity, blood vessels abnormally spread throughout the retina. The company's compound could potentially be a treatment.

  • A week doesn't go by without some Dendreon development. Washington CEO magazine covered the Dendreon saga in an article in its latest issue. The story doesn't break new ground but provides a thorough review of the controversy around Dendreon's Provenge prostate cancer treatment. Read the story here.

  • Posted by at May 5, 2008 10:39 a.m.
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