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Working Party on Similar Biological (Biosimilar) Medicinal Products (BMWP) of Committee for Medicinal Products for Human Use (CHMP).
The ODAC did not identify specific a hemoglobin target at which ESA therapy should begin, but recommended that FDA establish one.
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The researchers at the University of Rochester Medical Center in New York said theyve delved to the core of what are called Gprotein coupled receptors, which are complex molecules that transmit signals through cell membranes.
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Levin NW, Fishbane S, Ca単edo FV, Zeig S, Nassar GM, Moran JE, Villa G, Beyer U, Oguey D; MAXIMA study investigators Intravenous methoxy polyethylene glycol-epoetin beta for haemoglobin control in patients with chronic kidney disease who are on dialysis: a randomised non-inferiority trial (MAXIMA).
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According to the disclosure policy of the American Academy of CME Academy, all faculty, planning committee members, editors, managers, and other individuals who are in a position to control content are required to disclose any relevant relationships with any commercial interests related to this activity.
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CMS opened an internally generated National Coverage Decision (NCD) to evaluate coverage of uses of ESAs in non-renal disease applications.
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Pero las verdaderas curas para las enfermedades siguen siendo poco comunes.
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Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois; the Australian Graduate School of Management, University of New South Wales and the University of Sydney, Sydney, Australia; the Department of Nephrology, Tenon Hospital and Pierre and Marie Curie University, Paris, France; the Departments of Medicine and Oncology, McGill University Health Center, Montreal, Quebec, Canada; the University of New Mexico, VA Cooperative Studies Program, Albuquerque, New Mexico; the Division of Nephrology, David Geffen School of Medicine, University of California, Los Angeles, California; and Hotel Dieu Hospital and INSERM U362, Department of Hematology, Paris, France.
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