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ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

Does Saxagliptin Reduce the Risk of Cardiovascular Events When Used Alone or Added to Other Diabetes Medications

ClinicalTrials.gov ID: NCT01107886

Public ClinicalTrials.gov record NCT01107886. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicentre, Randomised, Double-Blind, Placebo-Controlled Phase IV Trial to Evaluate the Effect of Saxagliptin on the Incidence of Cardiovascular Death, Myocardial Infarction or Ischaemic Stroke in Patients With Type 2 Diabetes

Study identification

NCT ID
NCT01107886
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AstraZeneca
Industry
Enrollment
18,206 participants

Conditions and interventions

Interventions

  • Saxagliptin Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2010
Primary completion
Apr 30, 2013
Completion
Apr 30, 2013
Last update posted
Jul 16, 2014

2010 – 2013

United States locations

U.S. sites
202
U.S. states
43
U.S. cities
202
Facility City State ZIP Site status
Research Site Birmingham Alabama
Research Site Phoenix Arizona
Research Site Tempe Arizona
Research Site Tucson Arizona
Research Site Little Rock Arkansas
Research Site Alhambra California
Research Site Anaheim California
Research Site Bakersfield California
Research Site Burlingame California
Research Site Duarte California
Research Site Huntington Park California
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Research Site Bridgeport Connecticut
Research Site Bristol Connecticut
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Research Site Washington D.C. District of Columbia
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Research Site Endwell New York
Research Site New Hyde Park New York
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Research Site Charlotte North Carolina
Research Site Durham North Carolina
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Research Site Manassas Virginia
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Research Site Norfolk Virginia
Research Site Richmond Virginia
Research Site Burien Washington
Research Site Federal Way Washington
Research Site Tacoma Washington
Research Site Wenatchee Washington
Research Site Milwaukee Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 334 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01107886, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 16, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01107886 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →