Guest guest Posted November 9, 2008 Report Share Posted November 9, 2008 Hi, I was prowling the internet and found that Deciphera was ready to begin in the first quarter of 2009 as a new clinical trial for CML. Not much information is available as they are yet to start. I believe that MDACC will be one of the trial centers. I think it is exciting to have another drug about to make it's debut, which means another choice for us. Here is the introduction to DCC-2036. BCR-ABL Program Chronic Myelogeous Leukemia (CML) program DCC-2036 inhibits BCR-ABL kinase, an oncogenic fusion protein kinase resulting from chromosomal translocation (Philadelphia + chromosome). BCR-ABL is causative of myeloproliferative diseases, including chronic myelogenous leukemia (CML). http://www.deciphera.com/BCR-ABL.html. _____________________________________________ Singapore, Oct 6, 2008: Eli Lilly, a leading innovation-driven corporation and privately-held Deciphera Pharmaceuticals, have entered into a collaboration and worldwide licensing agreement related to latter's preclinical B-Raf kinase inhibitor program for the study of potential oncology therapeutics. The collaboration will advance their B-Raf kinase 'switch pocket' inhibitors into the clinic and ultimately to patients in need of these therapies. http://www.biospectrumasia.com/Content/061008OTH7294.asp Deciphera is pursuing two distinct strategies centered on B-RAF inhibition. The first strategy seeks potent and highly selective BRAF inhibitors. The second strategy pursues B-RAF inhibitors which also inhibit other kinases of interest. http://www.deciphera.com/inthenews.html ______________________________________________ Singapore, Nov 5, 2008: Melbourne based Mesoblast has commenced a phase I/II clinical trial in the US using the patented allogeneic, or " off-the-shelf " , Mesenchymal Precursor Cells (MPCs) in up to 30 patients with haematologic malignancies undergoing bone marrow transplantation. This follows clearance by the United States Food and Drug Administration (FDA) of an Investigational New Drug (IND) submission, and ethics approval by the Institutional Review Board (IRB) at the University of Texas M. D. Cancer Center in Houston. The trial will be funded through a grant awarded by the United States National Institutes of Health (NIH). http://www.biospectrumasia.com/content/051108AUS7572.asp This is a lot to read, but since this is a weekend, you can take your time. FYI, Lottie Quote Link to comment Share on other sites More sharing options...
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