Advances in the Management of Hematologic Diseases: Pipeline Drugs Become Clinical Reality
Release Date: June 23, 2009|
Expiration Date: June 23, 2010
1.5 AMA PRA Category 1 Credit(s)™|
May 30, 2009, Orlando, FL
This on-demand Webcast is from a satellite symposium held in conjunction with the 45th Annual Meeting of the American Society of Clinical Oncology held on May 29-June 2, 2009, in Orlando, FL.
The Advances in the Management of Hematologic Diseases: Pipeline Drugs Become Clinical Reality symposium has been designed to provide participants with leading-edge information on the novel, targeted anticancer therapies that are being developed for patients with hematologic malignancies, highlighting the mechanisms of action and the most current clinical data with these agents. This symposium will detail several of the key advancements in the rational targeting of proteins/processes that are disrupted in cancer and benign hematologic disorders, such as thrombopoiesis, fusion genes, and cell-cycle progression.
This educational activity is directed toward medical oncologists, translational researchers (both MDs and PhDs), drug developers from academia and industry, and other persons interested in cancer drug development. Fellows, nurses, physician assistants, and pharmacists are also invited to participate.
Upon completion of this educational activity, you should be able to:
You will be permitted 2 attempts to successfully complete the Posttest.
Complete the test(s) and evaluation by June 23, 2010 to receive your certificate online.
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These persons involved in the influence or control of content for the presentations from the Advances in the Management of Hematologic Diseases: Pipeline Drugs Become Clinical Reality symposium have disclosed the following relationship with the companies listed. The PER Scientific Content Team has no relevant financial relationships to disclose, unless noted below individually.
Morey Blinder, MD
Research Funding – Ligand Pharmaceuticals, Inc.
Bruce D. Cheson, MD, FACP
Paid Consultant – Astellas Pharma Inc., Celgene Corporation, Cephalon, Inc., EntreMed, Inc., Genentech, Inc., GlaxoSmithKline, Schering-Plough Corporation, Seattle Genetics, Inc.; Speaker’s Bureau – Genentech, Inc.
Ross Levine, MD
Paid Consultant – Novartis Pharmaceuticals Corporation
Keith R. McCrae, MD
Paid Consultant – GlaxoSmithKline; Speaker’s Bureau – Amgen, GlaxoSmithKline
PER Editorial Staff
No relevant relationships to disclose
This educational activity may contain discussion of published and/or investigational uses of agents that are not approved by the US Food and Drug Administration. For additional information about approved uses, including approved indications, contraindications, and warnings, please refer to the prescribing information for each product, or consult the Physician’s Desk Reference.
Commercial SupportAn educational grant for this activity was provided by Amgen.
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The views and opinions expressed in this learning activity are those of the presenters and do not necessarily reflect the views of the sponsor, supporter, or publisher. Although great care has been taken in compiling and checking the information given in this activity to ensure accuracy, the presenters and Physicians’ Education Resource and its servants or agents shall not be responsible or in any way liable for the continued currency of the information or for any errors, omissions, or inaccuracies in this activity, whether arising from negligence or otherwise howsoever or for any consequences arising therefrom.
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This activity is not sanctioned by, nor a part of, the 45th Annual Meeting of the American Society of Clinical Oncology.
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Editor, Advances in the Management of Hematologic Diseases: Pipeline Drugs Become Clinical Reality
Physicians’ Education Resource
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An educational grant for this activity was provided by: