Decreasing Cardiovascular Risk with Antihyperglycemic Agents in Patients with T2DM
New therapeutic options have emerged in the type 2 diabetes (T2DM) management paradigm that improve hyperglycemic control while decreasing cardiovascular risk. Watch this expert-led 90-minute panel discussion to learn about exciting new research on cardiovascular outcomes studies of antidiabetic agents and the resultant practical applications for patient care. Participants in this program will also receive expert advice on using ADA and AACE/ACE guidelines appropriately as well as other strategic insights to improve care for their patients with T2DM and cardiovascular risk.
Contracted Research for Amgen, Inc.; Arisaph Pharmaceuticals, Inc.; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Daiichi Sankyo; Janssen Pharmaceuticals, Inc.; Merck & Co., Inc.; and Takeda Pharmaceuticals U.S.A, Inc. Consulting Fees for Alnylam Pharmaceuticals Inc.; Amarin Pharma Inc.; Amgen, Inc.; Arisaph Pharmaceuticals, Inc.; AstraZeneca; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Eisai, Inc.; GlaxoSmithKline; Kowa Pharmaceuticals, Inc., Lipimetix Development Inc., Merck & Co., Inc., Pfizer Inc., Regeneron Pharmaceuticals, Inc., Sanofi US; and Takeda Pharmaceuticals U.S.A, Inc.
Advisory Board for Amarin Pharma Inc.; Amgen, Inc., AstraZeneca; Boehringer Ingelheim Pharmaceuticals, Inc.; Eisai Co.; Intarcia Therapeutics, Inc.; Janssen Pharmaceuticals, Inc.; Lilly; Merck & Co., Inc.; Novo Nordisk Inc.; Pfizer Inc.; Regeneron Pharmaceuticals, Inc.; and Sanofi US. Contracted Research for Amgen, Inc.; AstraZeneca; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Grifols; Janssen Pharmaceuticals, Inc.; Lexicon Pharmaceuticals; Merck & Co., Inc.; Novo Nordisk Inc.; and Sanofi US. Speaker’s Bureau for Amarin Pharma Inc.; Amgen, Inc.; AstraZeneca; Boehringer Ingelheim and Eli Lilly and Company; Janssen Pharmaceuticals, Inc.; Merck & Co., Inc.; Novo Nordisk Inc.; Regeneron Pharmaceuticals, Inc.; and Sanofi US.
Non-faculty contributors and others involved in the planning, development, and editing/review of the content have no relevant financial relationships to disclose.
pmiCME is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
pmiCME designates this enduring material for a maximum of 1.50 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
pmiCME is accredited by the American Association of Nurse Practitioners as an approved provider of nurse practitioner continuing education. Provider Number 040308.
This program has been approved for 1.50 contact hour of continuing education, including 0.90 of pharmacology.
Boehringer Ingelheim Pharmaceuticals, Inc. and Lilly USA, LLC
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Clinical judgment must guide each clinician in weighing the possible risks, benefits, or contraindications of any diagnostics, interventions or treatments discussed. Clinicians should review manufacturers’ product information and consider these with the recommendations of other authorities when applying the assessment and/or clinical management strategies discussed in this activity to the care of their patients.
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Discussion of Off-Label Uses and Investigational Products
During the course of their presentations, the faculty may mention uses of products that have not been approved in the United States for the indication(s) being discussed. All presenters are instructed to notify participants when they are discussing unapproved uses or investigational agents. In addition, specific slides will include notation of the off-label use or investigational agent being discussed. Views presented related to unapproved uses of products are solely those of the presenter(s) and are not endorsed by pmiCME or DBC Pri-Med, LLC.
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