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Biotech / Medical : Biotech success, 2002

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To: Miljenko Zuanic who started this subject3/13/2002 7:04:52 PM
From: Miljenko Zuanic   of 117
 
Wednesday March 13, 1:41 pm Eastern Time
Press Release
SOURCE: Cell Therapeutics (UK) Limited; Cell Therapeutics, Inc.
TRISENOX(R) Granted Marketing Authorization in Europe from the European Commission
LONDON, March 13 /PRNewswire-FirstCall/ -- Cell Therapeutics (UK) Limited, a wholly owned subsidiary of Cell Therapeutics, Inc. (CTI) (Nasdaq: CTIC - news), announced that the European Commission has granted the Marketing Authorization for TRISENOX (arsenic trioxide), indicated for the induction of remission and consolidation in adult patients with relapsed/refractory acute promyelocytic leukemia (APL) characterized by the presence of the t(15:17) translocation and/or the presence of the Pro-Myelocytic Leukemia/Retinioic-Acid-Receptor- alpha (PML/RAR-alpha) gene. Previous treatment should have included a retinoid and chemotherapy. U.S. Food and Drug Administration (FDA) also approved TRISENOX for the treatment of relapsed/refractory APL in September 2000 for marketing in the United States.
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