Healthcare Industry News: imatinib
News Release - November 14, 2006
ChemGenex Announces Granting of Fast Track Status for Ceflatonin(R) by FDAMELBOURNE, Australia & MENLO PARK, Calif.--(HSMN NewsFeed)--ChemGenex Pharmaceuticals (ASX: CXS, NASDAQ: CXSP) announced today that its investigational drug Ceflatonin® (homoharringtonine, HHT) has been awarded Fast Track status by the U.S. Food and Drug Administration (FDA). The Fast Track designation covers Ceflatonin® for the treatment of patients with chronic, accelerated and blast-phase chronic myeloid leukemia (CML) who have failed imatinib mesylate (Gleevec®) and have the T315I bcr-abl point mutation.
"The FDA decision to award Fast Track status to Ceflatonin® was based on recent clinical data and the high unmet need for new treatments for patients failing Gleevec® and Sprycel(TM)," said Greg Collier, Ph.D., Chief Executive Officer and Managing Director of ChemGenex. "As we enter the final stages of clinical development, with significant interest in our trials being conducted in both the United States and Europe, we look forward to collaborating closely with the FDA to expedite the development and approval of Ceflatonin®."
Ceflatonin® (HHT) is a potent inducer of apoptosis (programmed cell death) in myeloid cells and inhibits angiogenesis (blood vessel formation). In Phase 2 studies, Ceflatonin® has demonstrated clinical activity in patients with CML, both as a single agent and in combination with other chemotherapeutic drugs. ChemGenex is developing Ceflatonin® for the treatment of CML, and pilot studies are underway in myelodysplastic syndrome (MDS) and in acute myeloid leukemia (AML).
Ceflatonin® has a different mechanism of action than tyrosine kinase inhibitors (TKI's), and ongoing and proposed clinical studies will seek to determine;
1. Efficacy in treatment of CML patients who have developed resistance to tyrosine kinase inhibitor (TKI) therapy due to development of the T315I bcr-abl kinase domain point mutation. The T315I bcr-abl mutation, which develops in some CML patients treated with TKI's, is associated with resistance to Gleevec® and Sprycel(TM);
2. Efficacy in CML patients who have failed therapy with two tyrosine kinase inhibitors, e.g., Gleevec® and Sprycel(TM) and
3. Efficacy as combination therapy with Gleevec®, for the treatment of residual disease and to prolong Gleevec® sensitivity in CML patients who have developed resistance to Gleevec®.
Ceflatonin® is not approved by the FDA as a treatment in any indication and is currently being evaluated in clinical trials for efficacy and safety for future regulatory applications.
Ceflatonin® is a registered trade-mark of ChemGenex Pharmaceuticals Limited.
Gleevec® is a registered trade-mark of Novartis AG.
Sprycel(TM) is a registered trade-mark of the Bristol-Myers Squibb Company.
About ChemGenex Pharmaceuticals Limited (www.chemgenex.com)
ChemGenex Pharmaceuticals is a pharmaceutical development company dedicated to improving the lives of patients by developing therapeutics in the areas of oncology, diabetes, obesity, and depression. ChemGenex harnesses the power of genomics for target discovery and validation, and in clinical trials to develop more individualized therapeutic outcomes. ChemGenex's lead compound, Ceflatonin®, is currently in phase 2/3 clinical trials for chronic myeloid leukemia and Quinamed® is in phase 2 clinical development for prostate, breast and ovarian cancers. The company has a significant portfolio of anti-cancer, diabetes, obesity and depression programs, several of which have been partnered with international pharmaceutical companies. ChemGenex currently trades on the Australian Stock Exchange under the symbol "CXS" and on NASDAQ under the symbol "CXSP".
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Source: ChemGenex Pharmaceuticals
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