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David Greene
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Trading and investing full time for personal account and consulting with a money manager firm with assets of over $55 Million. Worked on Wall Street for 18 years at two wirehouses and one boutique investment banking firm. Investment discipline includes taking advantage of Wall Street's tendency... More
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  • Upcoming ASCO Abstract on Clinical Study of CTT's Pain Management Therapy Shows Better Than Expected Results 0 comments
    May 20, 2010 10:05 PM | about stocks: ABIO, ABT, CBST, AFFX, ARIA, ARYX, BAX, BCR, BDX, BSX, CELG, CMN, CNMD, CTIC, CTT-RETIRED, CYBX, DCTH, DNDN, ENZ, ETRM, GE, GILD, GNVC, GSK, HAE, IART, IBPI, IRIX, JNJ, KOOL, MAKO, MDT, MLNM, NVS, PDLI, PFE, PGNX, PHG, PMTI, RDNT, RTN, SOMX, SQNM, STJ, STS, SYK, VOLC, VVUS, WYE
    The abstract on Competitive Technologies' (NYSE Amex:CTT) Calmare Pain Management System's effectiveness on Chemotherapy-Induced Peripheral Neuropathy (CIPN) was posted on the website for the Annual Meeting of the  American Society of Clinical Oncology (OTC:ASCO) to be held from June 5-8. The clinical study of 16 patients saw "an overall 64% reduction in pain", significantly better than the study's primary goal of a 20% reduction in numeric pain scores.

    The conclusions by the authors was: "Patient-specific cutaneous electrostimulation with the MC5-A Calmare device appears to dramatically reduce pain in refractory CIPN patients with no toxicity."  Twenty-five percent (25%) of the patients had their CIPN pain enitirely alleviated. The presentation will be delivered at the ASCO meeting on June 8. Below is the abstract text:

    Pilot trial of a patient-specific cutaneous electrostimulation device (MC5-A Calmare) for chemotherapy-induced peripheral neuropathy

    Author(s): T. J. Smith, P. J. Coyne, P. Dodson, G. L. Parker, V. Ramakrishnan; Massey Cancer Center of Virginia Commonwealth University, Richmond, VA

    Abstract:

    Background: Chemotherapy-induced peripheral neuropathy (CIPN) is a major dose-limiting and persistent consequence of numerous classes of antineoplastic agents affecting up to 30-40% of patients (pts). To date, there is no highly effective prevention or therapy. An evolving hypothesis for reducing CIPN pain involves direct nerve stimulation to reduce the pain impulse. Methods: We evaluated the effect of the MC5-A Calmare therapy device on CIPN. The device is designed to generate a patient-specific cutaneous electrostimulation to reduce the abnormal pain intensity. Gel electrodes like EKG pads are applied below and above the dermatomes of pain. Pts with stable CIPN of > 5 pain, off chemotherapy, from one center received 1-hour interventions daily over 10 working days. NCT00952848. Results: The 16 pts had a mean age of 58.6 years; 4 men, 14 women; duration of CIPN all > 3 months up to 8 years. The most common drugs related to their neuropathy were taxanes, platinums, and bortezimib. The primary goal of a 20% reduction in numeric pain scores after day 10 was achieved in 15 of 16. The primary endpoint of CIPN pain score fell by 59% from day 1 to day 10. Adjusting for the correlations and the variability between patients and daily scores with a repeated measures analysis, there was an overall 64% reduction in pain. A daily treatment benefit was seen with a significant difference between the pre and post daily scores. Four patients had their CIPN reduced to 0. No toxicity was seen. Some responses have been durable without maintenance, and some patients had return of normal sensation and motor function. Conclusions: Patient-specific cutaneous electrostimulation with the MC5-A Calmare device appears to dramatically reduce pain in refractory CIPN patients with no toxicity. Further studies are underway to define the mechanisms of action, duration of benefit, and optimal schedule.

    Breakdown on results in chart form is included at the link below.

    Link to ASCO abstract: http://abstract.asco.org/AbstView_74_49144.html




    Disclosure: Long CTT
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