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    Cell Therapeutics May Be Banking Too Much on Lymphoma Drug

    Tue, 04/06/2010 - 06:02 EDT - Seeking Alpha
    • Zacks.com

    Zacks.com submits:
    April is crucial for Cell Therapeutics (CTIC), as the U.S. Food and Drug Administration (FDA) decides on the approvability of pixantrone by April 23, 2010. The company is seeking approval of its lead candidate, pixantrone for the treatment of relapsed or refractory aggressive non-Hodgkin’s Lymphoma (NHL) in patients who have not responded to other treatment options. However, we are not quite optimistic about the product gaining approval. Last month, the FDA’s Oncologic Drugs Advisory Committee unanimously decided against the approval of the candidate, citing lack of sufficient clinical data.Complete Story »

    • Original article
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      Zacks.com submits: In a positive development, Cell Therapeutics (CTIC) announced that the US Food and Drug Administration ((FDA)) has completed its inspection of the company’s manufacturing facility in Italy and found it to be compliant with all the required norms. The facility manufactures Cell Therapeutics’ Pixuvri (pixantrone), which is currently under FDA review.

    • FDA Likely to Deliver Blow to Cell Therapeutics

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    • Cell Therapeutics to Challenge FDA Decision

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    • Good News for Cell Therapeutics

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    • Cell Therapeutics: Product Developments in Line, But Liquidity Problems Remain

      Zacks.com submits: In an attempt to guard itself against hostile takeover, Cell Therapeutics (CTIC) adopted a shareholder rights plan. The plan, to be effective from Jan 7, 2010, has been designed so that a potential buyer has to discuss any offer with Cell Therapeutics' board of directors before approaching the shareholders directly.

    • Cell Therapeutics: Worth Buying Ahead of FDA Decision

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    • More Drama From Cell Therapeutics

      By M.E. Garza: Very early on Monday morning, Cell Therapeutics, Inc. (NASDAQ:CTIC) told Wall Street that they need additional time to prepare for the highly anticipated review of the Pixuvri NDA by the FDA's Oncologic Drugs Advisory Committee ("ODAC") at its February 9, 2012 meeting.

    • FDA Concerned About Forest Labs Drug: Biotech's Latest Missed Targets, Mishaps

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    • Cell Therapeutics' Pixantrone - Is Hope Coming For Patients And Patient Shareholders?

      By Brian Nichols:The Lancet is one of the more credible resources in the field of medicine and biotechnology with its three journals: infectious disease, neurology, and oncology. Writings from it tend to be well informed, well researched, well prepared, and highly objective for its readership.

    • Cell Therapeutics Still Waiting on Its Diagnosis

      The Burrill Report submits: Cell Therapeutics (CTIC) got a momentary reprieve from potentially bad news Friday as the US Food and Drug Administration postponed a meeting about pixantrone, an experimental treatment for refractory aggressive non-Hodgkin’s lymphoma, due to blustery weather.

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