Insulin Degludec Titration Using Mobile Insulin Dosing System

Inclusion Criteria

• •1. Subject has the ability to sign an informed consent form. Prior to randomization patients has signed the informed consent, approved by an Institutional Review Board/Independent Ethics Committee, and provided Health Insurance Portability and Accountability Act authorization (HIPAA) or other privacy authorization prior to any participation in study.
• •2. Subject 18 and older who has documented type 2 diabetes diagnosis at least 3 months before the screening
• •3. Subject has HbA1c \>/= 7.5% and \</=12.5 % measured using a NGSP certified method
• •4. Subject is initiating basal insulin therapy with insulin degludec or switching to insulin degludec from any basal insulin. The subject may also be on concomitant anti-hyperglycemic agents, including oral hypoglycemic (OAs), non-insulin injectables (e.g. GLP-1) which has been at a stable dose for approx. 3 months, or as determined by the Investigator
• •5. Subject is a male or non-pregnant, non-lactating female, at least 6 weeks postpartum prior to screening visit. A urine pregnancy test is required for all female subjects unless she is not of childbearing potential, defined as postmenopausal for at least one year prior to screening visit or surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy)
• •6. If female is of childbearing potential, is practicing one of the following methods of birth control (and will continue through the duration of the study):
• •1. Condoms, sponge, diaphragm, or intrauterine device;
• •2. Oral or parenteral contraceptives for 3 months prior to screening visit;
• •3. Vasectomized partner;
• •4. Total abstinence from sexual intercourse
• •7. Subject has a Glooko compatible smart device (smartphone/tablet) with an active data plan or access to Wi-Fi and downloaded at least one mobile application on their phone on their own. If subject does not have a Glooko compatible smart device, a loaner smart device can be provided for the study period.
• •8. Subject is currently performing self-monitoring of blood glucose(SMBG)