Guest guest Posted September 16, 2010 Report Share Posted September 16, 2010 August 4, 2010............. The clinical development program follows previously conducted Phase I and Phase II trials of Thiarabine in solid tumors, where myelosuppression (decrease in the production of blood cells), particularly lymphopenia (abnormally low white blood cell levels) was dose limiting. Access believes an agent that produces significant lymphopenia can be a strong active against lymphoproliferative disorders like acute lymphoblastic leukemia (ALL), chronic myelogenous leukemia (CML), myeloma and lymphoma. " We are pleased to have Dr. Kantarjian lead our continued clinical development of Thiarabine, " said Nowotnik, Access Pharmaceuticals, Inc.'s Senior Vice President for R & D. He continued, " The findings in preclinical and clinical studies to this point have given us a strong indicator that Thiarabine could be highly beneficial in treating patients with hematologic malignancies. The new Phase I/II trial at MD , one of the country's leading cancer centers, is the next step in our comprehensive plan to build on the strong set of data and clinical results that have been generated to date on Thiarabine. " http://www.medicalnewstoday.com/articles/196747.php Thiarabine Fact Sheet........... " Thiarabine exhibited significant activity, including regressions or cures, in six tested leukemia or lymphoma cell lines. The compound produced better activity than ara-C or a fatty acid-modified ara-C (depot) analog in four of six tested models. Thiarabine also performed as well or better than clofarabine and gemcitabine in each of the models. " Unlike ara-C, thiarabine was found to be active in a wide variety of solid tumor xenograft models (14 different cell lines), including colorectal, lung, renal, prostate, breast and pancreatic tumors, mainly via intraperitoneal administration (one model was done iv). Thiarabine produced regressions or tumor-free survivors in about half of the models and exhibited better activity than gemcitabine or clofarabine in many models. Thiarabine activity was also better than that of paclitaxel or cisplatin in certain lung models. An increase in regression or cure rate over either compound alone was observed with combinations of thiarabine and cisplatin in lung tumors, thiarabine and irinotecan or clofarabine in colorectal tumors, and thiarabine plus clofarabine in a leukemia model. " http://www.accesspharma.com/product-programs/thiarabine/ (posted to their website in 2009) ____________________________ July 29, 2010 (Written by ) American Association for Cancer Research " At the Hokkaido University Graduate School of Medicine, Yusuke Ohba, M.D., Ph.D., an associate professor, and colleagues tested the feasibility of a fluorescence resonance energy transfer biosensor in measuring the activity of leukemia cells. " Using this test, we are now able to identify and predict the most suitable treatment option for individual chronic myeloid leukemia patients, " said Ohba. " This technique is both sensitive and practical to use; it is especially useful for patients who are in relapse, a case in which the clinician's important decision regarding the next step in treatment must be made quickly and accurately. " " Working with laboratory cells, the researchers developed a series of assays that measured protein levels and known activity markers within CML lines. Using these measurements, they were able to identify not only the drug-resistant cells within the cultures, but also accurately determine the next therapeutic option, including dose escalation, combination therapy or second generation inhibitors. " The most critical issue in dealing with imatinib resistance is what to switch over to, " said Ohba. " If the patient is switched to another drug to which they are also resistant, then the treatment will just be a waste of time and detrimental to the patient's condition. " In an accompanying editorial also published in Clinical Cancer Research, Yingxiao Wang, Ph.D., an assistant professor in the bioengineering department at the University of Illinois Urbana-Champaign, said this study is a " pioneer work. " " The entire cancer community is talking about personalized medicine, and key to that is knowing when an individual person will have a unique response, " said Wang. " This project is an important step forward. " The trial was funded by the Japanese government, and none of the authors had a conflict of interest. The test is not available clinically in the United States. http://www.medicalnewstoday.com/articles/196176.php _____________________________ July 20, 2010 - Written by Kim Irwin University of California - Los Angeles " Scientists at the UCLA Broad Stem Cell Research Center have described a population of cells that mark the very first stage of differentiation of human embryonic stem cells as they enter a developmental pathway that leads to production of blood, heart muscle, blood vessels and bone. Researchers hope that these cells could one day be used for clinical treatments of a wide range of medical conditions as the discovery may help scientists create better and safer tissues for use in regenerative medicine. It also will allow scientists to better understand the differences between pluripotent stem cells, which can become every cell in the body, and cells that have lost their pluripotency and are on their way to becoming specific types of tissue cells. The study appears in the early online edition of the peer-reviewed journal Proceedings of the National Academy of Sciences. " http://www.medicalnewstoday.com/articles/195455.php ___________________________ BCR/ABL1 Quant Test (July 14,2010) This is a trade marked manufactured drug test by Asuragen. (Drug standardization tests) " Asuragen, Inc. and Life Technologies Corporation (NASDAQ: LIFE) announced that they have achieved CE-marking and commercial launch in Europe of the BCR/ABL1 Quant Test, Asuragen's clinically validated and cGMP manufactured test intended to aid clinicians in the monitoring and treatment of individuals afflicted with chronic myeloid leukemia (CML). Asuragen manufacturers the monitoring test, which is exclusively distributed by Life Technologies and runs on the company's Applied Biosystems CE-marked 7500 Fast Dx Real-Time PCR Instrument. " The CE-marked BCR/ABL1 Quant Test for leukemia progression is a quantitative in vitro diagnostic test to help doctors determine the most effective treatment options for CML. The test monitors the BCR-ABL1 to ABL1 ratio by reverse transcription quantitative polymerase chain reaction (RT-qPCR) on whole blood or bone marrow of diagnosed Philadelphia chromosome positive chronic myeloid leukemia (CML) patients expressing b2a2, b3a2 or e1a2 fusion transcripts. The test is intended as an aid in the assessment of complete cytogenetic response (CCyR), major molecular response (MMR), minimal residual disease and relapse in CML patients. " The BCR/ABL1 Quant Test provides several advantages over current methods by enabling multiplex detection of all targets in a single reaction and providing unmatched standardization through the use of our proprietary Armored RNA Quant® technology for external calibrators and process controls, " said Rollie Carlson, President of Asuragen. " http://www.medicalnewstoday.com/articles/194588.php _____________________________ FYI, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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