Saturday, September 15, 2012

Cell Therapeutics gains Approval in Europe for Pixuvri™

Cell Therapeutics, Inc. (NASDAQ:CTIC) has traded as high as $1.65 during today�s trading session and last traded at $1.40 for a gain of 26.13% from yesterday�s close� CTIC shares have traded as high as $3.33 over the past 52 weeks, which is 57.95% off that high at last traded stock price. Get my next ALERT 100% FREE

Cell Therapeutics announced today that Pixuvri� (pixantrone dimaleate) has been granted a positive opinion for conditional approval from the European Medicines Agency’s (“EMA”) Committee for Medicinal Products for Human Use (“CHMP”). Based on the CHMP’s recommendation, CTI expects that a conditional marketing authorization for Pixuvri should be granted by the European Commission within the next few months. CHMP recommended Pixuvri for conditional approval as monotherapy for the treatment of adult patients with multiple relapsed or refractory aggressive non-Hodgkin B-cell lymphomas (“NHL”).

If the CHMP’s recommendation is formally adopted by the European Commission, Pixuvri would be approved for marketing in the 27 countries that are members of the E.U., as well as the European Economic Area.� The decision by the European Commission is typically issued approximately two to three months after the CHMP opinion and generally follows the recommendation from the CHMP. If the opinion is confirmed by the European Commission, Pixuvri would be the first drug approved for patients in this setting.

“We are very pleased with the CHMP’s positive recommendation recognizing the clinical benefit of Pixuvri in addressing a significant unmet medical need for patients with multiple relapsed or refractory aggressive B-cell NHL, and we believe that Pixuvri will add an important treatment option for physicians and provide a meaningful impact on patients,” stated James A. Bianco, CEO of CTI.

“There are currently no proven effective therapies for these advanced NHL patients. Our goal for this late stage patient population is to control disease progression and symptoms as a cure is no longer an option. We are encouraged by the PFS noted in the PIX301 study and the opportunity this agent provides in treating this difficult to treat group of patients,” said Bertrand Coiffier, M.D., Ph.D., Professor of Hematology at the Department of Hematology, Hospices Civils de Lyon and the University Lyon 1 in Lyon, France.

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