Sodium-Glucose Transporter 2 Inhibitors: New Therapeutic Targets, New Therapeutic Options in the Treatment of Type 2 Diabetes Mellitus CME

Author Information and Disclosures

Release Date: March 31, 2008Valid for credit through March 31, 2009

Credits Available
Physicians - maximum of 1.0 AMA PRA Category 1 Credit(s) for physicians

To participate in this internet activity: (1) review the target audience, learning objectives, and author disclosures; (2) study the education content; (3) take the post-test and/or complete the evaluation; (4) view/print certificate View details.

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BMS, AstraZeneca

Learning Objectives

Upon completion of this activity, participants will be able to:

  1. Review the pathophysiology of type 2 diabetes in the context of the need for new drugs in the armamentarium for glycemic control
  2. Review the role of the kidney in maintaining normal glucose homeostasis
  3. Examine the potential of SGLT2 inhibition in the treatment of type 2 diabetes
Authors and Disclosures

John P.H. Wilding, DM, FRCP
Disclosure: John P.H. Wilding, DM, FRCP, has disclosed that he has served as an advisor or consultant to AstraZeneca, Bristol-Myers Squibb, and GlaxoSmithKline. Dr. Wilding has also disclosed that he has received grants for clinical research from AstraZeneca and Bristol-Myers Squibb.


Dick De Zeeuw, MD, PhD
Disclosure: Dick De Zeeuw, MD, PhD, has disclosed that he has received grants for clinical research from AstraZeneca.


Kristin M. Richardson
Disclosure: Kristin M. Richardson has disclosed no relevant financial relationships.


 
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