This site became the new on June 19th. Learn more.
Show more Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu
Give us feedback

The Efficacy and Safety Study in Patients With Type 2 Diabetes Mellitus (SUNSHINE)

This study has been completed.
Information provided by (Responsible Party):
AstraZeneca Identifier:
First received: May 28, 2012
Last updated: December 31, 2015
Last verified: December 2015
The efficacy and safety study of saxagliptin 5mg, once daily for 24 weeks in patients with type 2 diabetes mellitus.

Condition Intervention Phase
Diabetes Mellitus, Non-Insulin-Dependent Drug: Saxagliptin Phase 4

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Multicenter, Single Arm, Cohort Study to Evaluate the Efficacy and Safety of Saxagliptin 5mg, Once Daily for 24 Weeks, in Patients With Type 2 Diabetes Mellitus

Resource links provided by NLM:

Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • Absolute Change From Baseline in Haemoglobin A1c (HbA1c) [ Time Frame: Weeks 6, 12, and 24 ]
    Evaluation after 24 weeks oral administration of saxagliptin treatment in patients with type 2 diabetes inadequately controlled with diet and exercise or with metformin in addition to diet and exercise.

Secondary Outcome Measures:
  • Proportion (%) of Patients Achieving HbA1c <7% [ Time Frame: Weeks 6, 12, and 24 ]
  • Change From Baseline in Fasting Plasma Glucose (FPG) [ Time Frame: Weeks 6, 12, 18, and 24 ]
  • Change From Baseline in 2-hour Postprandial Plasma Glucose (2h-PPG) [ Time Frame: Week 24 ]

Enrollment: 2165
Study Start Date: November 2012
Study Completion Date: May 2014
Primary Completion Date: May 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Open label
Saxagliptin, oral 5mg once a day(Q. D.)
Drug: Saxagliptin
oral, 5 mg once a day (Q.D.)
Other Name: Onglyza

Detailed Description:
A multicenter, single arm, cohort study to evaluate the Efficacy and Safety of saxagliptin 5mg, once daily for 24 weeks, in patients with type 2 diabetes mellitus who are treatment naive or who have inadequate glycaemic control on metformin alone

Ages Eligible for Study:   18 Years to 99 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Provision of informed consent prior to any study specific procedures Diagnosed with type 2 diabetes
  • Men or women who are >18 years of age at time of consenting upon Visit 1
  • HbA1c >7.5% and ≤11.0% Patients should be drug naive or treated with metformin alone on stable doses of for at least continues 8 weeks prior to Visit 1
  • Drug naive patients are defined as patients who have not received medical treatment for diabetes (insulin and/or oral hypo)

Exclusion Criteria:

  • Pregnant or breastfeeding patients
  • Insulin therapy within one year of enrolment (with the exception of insulin therapy during a hospitalization or use in gestational diabetes)
  • Previous treatment with any DPP-IV inhibitors or GLP-1 analogue
  • History of administration of any antihyperglycemic therapy (other than metformin) during the 8 weeks prior to Visit 1(12 weeks for previous TZD)
  • Treatment with systemic glucocorticoids other than replacement therapy
  • Inhaled, local injected and topical use of glucocorticoids is allowed
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01608724

Research Site
Baotou, China
Research Site
Beijing, China
Research Site
Benxi, China
Research Site
Changchun, China
Research Site
Chengdu, China
Research Site
Chongqing, China
Research Site
Dalian, China
Research Site
Dongguan, China
Research Site
Foshan, China
Research Site
Fuzhou, China
Research Site
Guangzhou, China
Research Site
Guiyang, China
Research Site
Haikou, China
Research Site
Hangzhou, China
Research Site
Hhht, China
Research Site
Hubei, China
Research Site
Jimo, China
Research Site
Jinan, China
Research Site
Kunming, China
Research Site
Linyi, China
Research Site
Nanjing, China
Research Site
Nantong, China
Research Site
Qingdao, China
Research Site
Shanghai, China
Research Site
Shantou, China
Research Site
Shenyang, China
Research Site
Shiyan, China
Research Site
Suzhou, China
Research Site
Taiyuan, China
Research Site
Tianjin, China
Research Site
Urumqi, China
Research Site
Wenzhou, China
Research Site
Wuhan, China
Research Site
Wuxi, China
Research Site
Xian, China
Research Site
Zhanjiang, China
Research Site
Zhengzhou, China
Sponsors and Collaborators
Study Director: Simon Fisher AstraZeneca
  More Information

Responsible Party: AstraZeneca Identifier: NCT01608724     History of Changes
Other Study ID Numbers: D1680L00008
Study First Received: May 28, 2012
Results First Received: May 14, 2015
Last Updated: December 31, 2015

Keywords provided by AstraZeneca:
Type 2 DM

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Dipeptidyl-Peptidase IV Inhibitors
Protease Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Hypoglycemic Agents processed this record on August 16, 2017