Morphea-like skin lesions reported in the phase 3 Long-Term Odanacatib Fracture Trial (LOFT) in postmenopausal women with osteoporosis - 18/02/21
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Funding sources: Funding for this research and medical writing assistance was provided by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, New Jersey, USA. |
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Disclosure: Dr Saag has received research grants from Amgen, Mereo, Merck Sharp & Dohme Corp. (MSD), and Radius, and consulting fees from Amgen, MSD, Radius, and Roche. Dr de Villiers has received consulting/speaker fees from Abbott, Amgen, Aspen, Adcock Ingram, MSD, and Pfizer. Drs Jacobe, Kovarik, and Werth have received consulting fees from MSD. Dr Leung, Authors Desai-Merchant and Julie Mattaliano, and Dr Deborah Gurner are current or former employees of MSD, a subsidiary of Merck & Co., Inc., Kenilworth, New Jersey, and may own stock and/or hold stock options in Merck & Co., Inc., Kenilworth, New Jersey. |
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This material was presented during an oral presentation at the American College of Rheumatology (ACR) 2016 Annual Meeting, November 11–16, 2016, Washington, DC, and included in the associated abstract. |
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IRB approval status: The study was approved by local institutional review boards and ethics review committees at all centers, as noted in the primary publication. |
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