ChemGenex Launches Multi-Center Phase 2 Clinical Trial of Ceflatonin in Combination with Gleevec in Patients with Chronic Myelogenous Leukemia.MELBOURNE, Australia & MENLO PARK Menlo Park. 1 Residential city (1990 pop. 28,040), San Mateo co., W Calif.; inc. 1874. Electronic equipment and aerospace products are manufactured in the city. Menlo College and a Stanford Univ. research institute are there. 2 Uninc. , Calif. -- ChemGenex Pharmaceuticals Limited (ASX ASX See: Australian Stock Exchange :CXS CXS Coherent X-Ray Scattering ) announced today that it has launched a multi-center Phase 2 study evaluating the use of Ceflatonin(R) (homoharringtonine or HHT HHT Hereditary Hemorrhagic Telangiectasia (Osler-Rendu-Weber disease) HHT Headquarters Troop HHT Hand-Held Terminal HHT House Hunting Trip HHT Heinrich Hertz Telescope HHT Headquarters & Headquarters Troop ) in combination with Gleevec(R) (imatinib mesylate imatinib mesylate Warning - Hazardous drug! Gleevec, Glivec (UK) Pharmacologic class: Protein-tyrosine kinase inhibitor Therapeutic class: Antineoplastic ), in patients with chronic myelogenous leukemia Chronic myelogenous leukemia (CML) Also called chronic myelocytic leukemia, malignant disorder that involves abnormal accumulation of white cells in the marrow and bloodstream. Mentioned in: Bone Marrow Transplantation (CML 1. CML - A query language. ["Towards a Knowledge Description Language", A. Borgida et al, in On Knowledge Base Management Systems, J. Mylopoulos et al eds, Springer 1986]. 2. CML - Concurrent ML. ) who have developed resistance to Gleevec(R). Dr. Jorge Cortes, Professor of Leukemia at the M.D. Anderson Cancer Center in Houston, Texas “Houston” redirects here. For other uses, see Houston (disambiguation). Houston (pronounced /'hjuːstən/) is the largest city in the state of Texas and the , is the principal investigator Noun 1. principal investigator - the scientist in charge of an experiment or research project PI scientist - a person with advanced knowledge of one or more sciences for the study. Gleevec(R) is a targeted therapeutic with global sales in excess of US$1.6 billion in 2004. Gleevec(R) was first approved in 2001 for the treatment of advanced-stage CML patients, and it remains the dominant therapy for CML globally. Despite Gleevec(R)'s effectiveness in early stage CML, responses in late (blastic) phase patients are usually short-lived (3-6 months median duration), with only 15% of patients experiencing a durable response. When used in earlier (chronic) stages of the disease, approximately 20% of patients have primary resistance to Gleevec(R) and a further 20% of patients develop resistance after 14 months. While Gleevec(R) and other investigational tyrosine kinase inhibitors have generated excellent results, there is still a need to improve therapy in CML. Agents with novel mechanisms of action are needed to treat patients who fail or develop resistance to tyrosine kinase inhibitors like Gleevec(R). Moreover, agents with synergistic mechanisms of action are needed for use in-combination with tyrosine kinase inhibitors to limit resistance and increase the chances of a cure. "Ceflatonin(R) is an attractive agent to combine with Gleevec(R) because it has confirmed Phase 2 single agent activity in refractory CML. We also know that it has a complementary mechanism of action that can reduce Bcr-Abl protein expression associated with Gleevec(R) resistance," said Greg Collier, Ph.D., Chief Executive Officer and Managing Director of ChemGenex. "Our objective in this study is to induce a good patient response while at the same time reducing the Bcr-Abl proteins associated with resistance to Gleevec(R) and CML disease progression." Ceflatonin(R) Clinical and Preclinical Activity Laboratory and human studies have demonstrated that HHT is active in patients with CML who have become resistant to Gleevec(R): --In a recent Phase 1 safety study sponsored by the National Cancer Institute (NCI See Liberate. ) at the M.D. Anderson Cancer Center in Houston, Texas, 10 patients in the advanced stages of CML who no longer responded to Gleevec(R) were treated with HHT. The investigators observed no significant toxicities and five (50%) of the patients responded to HHT therapy. --In preclinical studies preclinical studies, n.pl a term used to describe research done before a clinical study. May be laboratory or epidemiologic research. , HHT showed synergistic activity with Gleevec(R) as measured by a reduction in the marker (Bcr-Abl protein expression) that is a hallmark of Gleevec(R) resistance in CML. These studies confirm that Ceflatonin(R) shows promise against CML, both as a single agent therapy in advanced stages of the disease and in combination with Gleevec(R) for earlier stage disease. Clinical Trial Details The trial will be an open-label, multi-center study for patients with CML, whose disease is in chronic, accelerated, or blast phase. Patients will receive 2.5 milligrams per meter squared Ceflatonin(R) by continuous 24-hour intravenous infusion, daily for 5 days (days 1 - 5 of each treatment cycle) every 4 weeks. They will also receive Gleevec(R) 400 mg daily for CML patients in chronic phase, and 600 mg daily for CML patients in accelerated and blast phases. About ChemGenex Pharmaceuticals Limited (www.chemgenex.com) ChemGenex Pharmaceuticals is a gene-based pharmaceutical company dedicated to improving the lives of patients by developing therapeutics in the areas of oncology, diabetes, obesity, and depression. ChemGenex currently has two compounds in Phase 2 clinical trials phase 2 clinical trial Phase 2 study. See Phase study. , Ceflatonin(R) for leukemia and Quinamed(R) for solid tumors, and has a significant portfolio of anti-cancer, diabetes, obesity and depression programs. The company's diabetes and obesity program is partnered with Merck KGaA and the depression program is partnered with Vernalis plc. ChemGenex currently trades on the Australian Stock Exchange Australian Stock Exchange (ASX) Australia's major securities market, formed when the six state stock exchanges (Adelaide, Brisbane, Hobart, Melbourne, Perth, and Sydney stock exchanges) were merged in 1987. under the symbol "CXS." Gleevec(R) is a registered trade-mark of Novartis AG. Safe Harbor Safe Harbor 1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated. 2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive. Statement Certain statements made herein that use the words "estimate," 'project," "intend," "expect," "believe," and similar expressions are intended to identify forward-looking statements within the meaning of the US Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and of 1995. These forward-looking statements involve known and unknown risks and uncertainties which could cause the actual results, performance or achievements of the company to be materially different from those which may be expressed or implied by such statements, including, among others, risks or uncertainties associated with the development of the company's technology, the ability to successfully market products in the clinical pipeline, the ability to advance promising therapeutics through clinical trials, the ability to establish our fully integrated technologies, the ability to enter into additional collaborations and strategic alliances and expand current collaborations and obtain milestone payments, the suitability of internally discovered genes for drug development, the ability of the company to meet its financial requirements, the ability of the company to protect its proprietary technology, potential limitations on the company's technology, the market for the company's products, government regulation in Australia and the United States, changes in tax and other laws, changes in competition and the loss of key personnel. These statements are based on our management's current expectations and are subject to a number of uncertainties that could change the results described in the forward-looking statements. Investors should be aware that there are no assurances that results will not differ from those projected. |
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