Overcoming Barriers to Injectable Therapies
Individualizing Antihyperglycemic Regimens in T2DM
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) and basal insulin analogs are essential antihyperglycemic therapies for many patients with type 2 diabetes mellitus (T2DM) (eg, those in need of large glucose-lowering effects or, based on recent updates to the official indications for 2 of the GLP-1 RAs). This Engaging the Patient activity will discuss newer insulin therapies as well as GLP-1 injectable therapies, including rationales and clinical trial evidence for combining these two agents. The activity includes a demonstration of clinician and patient interactions-ways to educate patients on the use of injectable medications, as well as approaches to reducing hypoglycemia and improving patient adherence.
Advisory Board for Abbott Laboratories; Janssen Pharmaceuticals, Inc.; Lilly; and Novo Nordisk Inc. Services Provided for Promotional Purposes (not for CME/CE) for Abbott Laboratories; Janssen Pharmaceuticals, Inc.; Lilly; and Novo Nordisk Inc. Speaker’s Bureau for Abbott Laboratories; Janssen Pharmaceuticals, Inc.; Lilly; and Novo Nordisk Inc.
Advisory Board for Ironwood Pharmaceuticals, Inc. and Merck & Co., Inc. Speaker’s Bureau for Ironwood Pharmaceuticals, Inc.; Merck & Co., Inc.; and Takeda Pharmaceuticals U.S.A., Inc.
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 1.00 AMA PRA Category 1 Credit™. 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 1.00 contact hour of continuing education, which includes 0.61 hour of pharmacology.
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Novo Nordisk Inc.
Integritas Communications, 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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Pri-Med programs are owned and operated by DBC Pri-Med, LLC, a division of Diversified Communications, Inc. pmiCME, the accredited division of Pri-Med, is accredited with commendation by the ACCME and approved as a provider of continuing education by the AANP. pmiCME is the accredited provider for this activity.
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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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