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CTI Announces Data Presentations at the 18th Congress of the European Hematology Association
Date:6/10/2013

Safe Harbor Statement

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 market price of CTI's securities. Specifically, the risks and uncertainties that could affect the development of PIXUVRI and pacritinib include risks associated with preclinical and clinical developments in the biopharmaceutical industry in general and with PIXUVRI and pacritinib in particular including, without limitation, the potential failure of PIXUVRI to prove safe and effective for the treatment of relapsed or refractory NHL and/or other tumors as determined by the U.S. Food and Drug Administration (FDA); that results in future studies of PIXUVRI may differ from the results of past studies; that CTI may not be able to complete the PIX306 clinical trial of PIXUVRI-rituximab compared to gemcitabine-rituximab in patients who have relapsed after 1 to 3 prior regimens for aggressive B-cell NHL and who are not eligible for autologous stem cell transplant by June 2015 or at all as required by the European Medicines Agency (EMA) or have the results of such trial available by June 2015 or at all; that CTI may not be able complete a post-marketing study aimed at confirming the clinical benefit of PIXUVRI that was observed in the PIX301 trial; that the conditional marketing authorization for PIXUVRI may not be renewed; the potential failure of pacritinib to prove safe and effective for the treatment of patients with myelofibrosis, either alone or in combination regimens, as determined by the FDA and/or EMA; that pacritinib may not satisfy a medical need not currently addressed with existing non-selective JAK1/JAK2 inhibitors; that the Phase III clinical trials of pacritinib may not occur as planned; that CTI may not be able to successfully implement its plans, strategies and objectives related to the development of p
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SOURCE Cell Therapeutics, Inc.
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