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Cell Therapeutics, Inc. (CTI) Reports Fourth Quarter and Year-End Financial Results and Milestones
Date:3/6/2012

ls of Oncology. 2010: 5: 172-174.

This press release includes forward-looking statements that involve a number of risks and uncertainties, the outcome of which could materially and/or adversely affect actual future results and the trading price of CTI's securities. Specifically, the risks and uncertainties that could affect the development of CTI's drug candidates include risks associated with preclinical and clinical developments in the biopharmaceutical industry in general, and with pixantrone in particular, including, without limitation, the potential failure of pixantrone to prove safe and effective for the treatment of relapsed or refractory aggressive NHL and/or other tumors as determined by the FDA and/or the EMA, that Pixuvri may not be the first drug approved as monotherapy for the treatment of adult patients with multiple relapsed or refractory aggressive NHL, that the European Commission may not formally adopt the CHMP's recommendation regarding Pixuvri, that conditional approval of CTI's MAA for Pixuvri may not be granted by the European Commission within the next few months or at all, that Pixuvri may not be approved for marketing in all of the E.U. Member States and the European Economic Area members, that the EMA may request additional information from CTI regarding Pixuvri, the potential failure of tosedostat to prove safe and effective for the treatment of relapsed MDS, AML, multiple myeloma, blood related cancers and solid tumors as determined by the FDA and/or the EMA, that the FDA may not accept the proposed clinical trial of tosedostat and/or may request additional trials, that CTI may not meet with the FDA in March 2012 regarding the phase 3 clinical trial of tosedostat in MDS, that CTI may not acquire any additional novel clinical stage compounds to expand its hematologic cancer product pipeline, that CTI cannot predict or guarantee the pace or geography of enrollment of its clinical trials, that CTI may not
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