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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 Oct 27, 2026, 3:15 PM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether saxagliptin can reduce the risk of cardiovascular events when used alone or added to other diabetes medications

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

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
May 2010 (Type not available)
Primary completion
May 2013 (Actual)
Completion
May 2013 (Actual)
Last update posted
Jul 17, 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 — —
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Research Site Beachwood Ohio — —
Research Site Cadiz Ohio — —
Research Site Canal Fulton Ohio — —
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Research Site Hermitage Pennsylvania — —
Research Site Indiana Pennsylvania — —
Research Site Jersey Shore Pennsylvania — —
Research Site Johnstown Pennsylvania — —
Research Site Philadelphia Pennsylvania — —
Research Site Pittsburgh Pennsylvania — —
Research Site Sayre Pennsylvania — —
Research Site Tyrone Pennsylvania — —
Research Site Providence Rhode Island — —
Research Site Charleston South Carolina — —
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Research Site Greer South Carolina — —
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Research Site Burke 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 17, 2014 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01107886 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →