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Efficacy and Safety of Vildagliptin in Subjects With Impaired Glucose Tolerance

Primary Purpose

Prediabetic State

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
vildagliptin
Sponsored by
Novartis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prediabetic State focused on measuring Pre-diabetes, vildagliptin, IGT

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All Sexes

Inclusion Criteria: Blood glucose criteria must be met Body mass index (BMI) in the range 23-45 Exclusion Criteria: Diagnosis of diabetes Serious cardiovascular events within the past 6 months Use of insulin or any oral antidiabetic agent Other protocol-defined exclusion criteria may apply

Sites / Locations

  • Novartis Pharmaceuticals

Outcomes

Primary Outcome Measures

Change in area under the 0-2 hour prandial glucose curve at 12 weeks

Secondary Outcome Measures

Adverse event profile after 12 weeks of treatment
Change in ratio for postprandial insulin AUC and postprandial glucose AUC (0-2 hours) after 12 weeks of treatment
Change in HOMA B at 12 weeks
Change in fasting insulin at 12 weeks
Change in fasting proinsulin/insulin ratio at 12 weeks

Full Information

First Posted
October 9, 2005
Last Updated
May 4, 2012
Sponsor
Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT00237250
Brief Title
Efficacy and Safety of Vildagliptin in Subjects With Impaired Glucose Tolerance
Official Title
Efficacy and Safety of Vildagliptin in Subjects With Impaired Glucose Tolerance
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
July 2006 (Actual)
Study Completion Date
July 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Novartis

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to assess the safety and effectiveness of vildagliptin, an unapproved drug, compared to placebo in lowering post-meal blood glucose levels in people with pre-diabetes who have high blood sugar levels after meals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetic State
Keywords
Pre-diabetes, vildagliptin, IGT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
171 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
vildagliptin
Primary Outcome Measure Information:
Title
Change in area under the 0-2 hour prandial glucose curve at 12 weeks
Secondary Outcome Measure Information:
Title
Adverse event profile after 12 weeks of treatment
Title
Change in ratio for postprandial insulin AUC and postprandial glucose AUC (0-2 hours) after 12 weeks of treatment
Title
Change in HOMA B at 12 weeks
Title
Change in fasting insulin at 12 weeks
Title
Change in fasting proinsulin/insulin ratio at 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Eligibility Criteria
Inclusion Criteria: Blood glucose criteria must be met Body mass index (BMI) in the range 23-45 Exclusion Criteria: Diagnosis of diabetes Serious cardiovascular events within the past 6 months Use of insulin or any oral antidiabetic agent Other protocol-defined exclusion criteria may apply
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Novartis Pharmaceuticals
Organizational Affiliation
Novartis Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Novartis Pharmaceuticals
City
East Hanover
State/Province
New Jersey
ZIP/Postal Code
07936
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17947341
Citation
Rosenstock J, Foley JE, Rendell M, Landin-Olsson M, Holst JJ, Deacon CF, Rochotte E, Baron MA. Effects of the dipeptidyl peptidase-IV inhibitor vildagliptin on incretin hormones, islet function, and postprandial glycemia in subjects with impaired glucose tolerance. Diabetes Care. 2008 Jan;31(1):30-5. doi: 10.2337/dc07-1616. Epub 2007 Oct 18.
Results Reference
derived

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Efficacy and Safety of Vildagliptin in Subjects With Impaired Glucose Tolerance

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