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Additionally, non-clinical data will be presented evaluating the result of AC220 monotherapy and in conjunction with chemotherapy. ‘AML continues to be a disease with a significant unmet medical need and brand-new therapies are urgently needed,’ said M. Scott Salka, Chief Executive Officer of Ambit Biosciences. ‘The Phase I scientific data we’ve seen for AC220 in AML are extremely encouraging and works with the further advancement of the highly selective second-era FLT3 inhibitor.’ Related StoriesPenn research forms basis for new treatment approaches for Sezary syndromePotential fresh drug target for acute myeloid leukemiaDr. Paul Liu called 2015 Distinguished Alumnus for contributions to leukemia researchData Highlights for AC220 include: ORAL PRESENTATIONS Abstract #636 AC220, a Potent, Selective, Second Era FLT3 Receptor Tyrosine Kinase Inhibitor, in a First-in-Human Stage 1 AML Study Offered by: Jorge Cortes, MD Session Name: Acute Myeloid Leukemia – Therapy, excluding Transplantation II Day: Monday, 7 December, 2009, 5:45pm , Morial Convention Middle Space 343-345 POSTER PRESENTATIONS Abstract# 2053 AC220 – A FLT3 Inhibitor, Boosts Survival in Two Genotypically Distinct FLT3-ITD Models of Acute Myeloid Leukemia and Sustained Protection Following Chronic Administration Session Name: Acute Myeloid Leukemia – Therapy, sunday excluding Transplantation II, December 6, 2009, 6:00 – 8:00pm, Hall E, Poster Board II-45 Abstract#: 2052 AC220, a Potent and Particular FLT3 Inhibitor, Enhances the Cytotoxic Effects of Chemotherapeutic Agents in Cell Tradition and in Mouse Tumor Xenograft Program Name: Acute Myeloid Leukemia – Therapy, excluding Transplantation II Sunday, December 6, 2009, 6:00 PM – 8:00 PM, Hall E, Poster Board II-44..