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Incyte Corporation Message Board

  • maddison3 maddison3 Nov 5, 2012 9:25 AM Flag

    ASH abstracts

    Due out today...according to Rich Levy. Shorts you have been warned. These abstracts will highlight long term survival for Jakafi. TJ, what do you think about stock price this week! Also big conference this coming weekend with Lilly on 050. This will be dynamite. My prediction for week is we close much who knows....IMHO

    Sentiment: Strong Buy

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    • I searched the ASH website and cannot locate the abstract on Jakafi. Has anyone had more success and can you post? Leaving now to vote....can't wait for results.... 4 more years? NO

      Sentiment: Strong Buy

      • 1 Reply to maddison3
      • Here is an important abstract of the low platelet treatment study which should expand the labeling of Jakafi next year.
        Background: Ruxolitinib (RUX) has demonstrated clinical benefit for patients with myelofibrosis (MF) with or without the JAK2V617F mutation at starting doses of 15 or 20 mg PO BID by alleviating symptoms, improving quality of life measures, reducing spleen volume and exhibiting an apparent increase in overall survival in the phase III placebo (PBO)-controlled COMFORT-I study. Reversible declines in platelet count and hemoglobin (Hgb) can occur with ruxolitinib but are rarely treatment-limiting. Patients with MF who have low platelet counts represent an important subset of MF patients; given the potential risk of bleeding complications, a dosing strategy for such patients is needed. We assessed an alternative strategy using lower starting doses of ruxolitinib with subsequent dose escalation in patients with MF who have platelet counts of 50–100 x 109/L (Study INCB018424-258; NCT01348490).
        Methods: RUX dosing started at 5 mg BID. With adequate platelet count, doses could increase by 5 mg once daily every 4 weeks to 10 mg BID. Further increases required evidence of suboptimal efficacy. Assessments include measurement of MF symptoms (MF Symptom Assessment Form v2.0 Total Symptom Score [TSS]); Patient Global Impression of Change (PGIC); EORTC QLQ-C30, measurement of spleen volume by MRI, and safety/tolerability.
        Results: A total of 50 patients have enrolled, with data available for 41 patients. Nineteen have completed 24 weeks of treatment; 70% of these patients attained a final dose of ≥10 mg BID of RUX. Treatment was generally well tolerated in this study population with no withdrawals for thrombocytopenia or bleeding events. Based on analysis of adverse events, no new safety signals were observed in this population of MF patients with low platelet counts. Data for efficacy parameters, including spleen volume reduction, TSS reduction, and improvement in EORTC-QLQ-C30 subscales and PGIC were consistent with RUX treatment in the COMFORT-I study, and demonstrated clinically

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