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A 56-Week Extension to a Clinical Study to Assess the Efficacy and Safety of Vildagliptin Compared to Placebo in Drug Naive Patients With Type 2 Diabetes and Mild Hyperglycemia

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Vildagliptin
Sponsored by
Novartis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Type 2 diabetes, Vildagliptin

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All Sexes

Inclusion Criteria: Completion of study CLAF237A2307 within 4 weeks of entering into the extension Written informed consent Ability to comply with all study requirements Blood glucose criteria must be met Exclusion Criteria: Premature discontinuation from study CLAF237A2307

Sites / Locations

Outcomes

Primary Outcome Measures

Change from baseline in HbA1c at 108 weeks

Secondary Outcome Measures

Adverse event profile after 108 weeks of treatment
Change in HbA1c from week 52 to week 108
Change from baseline in fasting plasma glucose at week 108
Change in fasting plasma glucose from week 52 to week 108
Change from baseline in body weight at week 108

Full Information

First Posted
March 6, 2006
Last Updated
July 31, 2017
Sponsor
Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT00300287
Brief Title
A 56-Week Extension to a Clinical Study to Assess the Efficacy and Safety of Vildagliptin Compared to Placebo in Drug Naive Patients With Type 2 Diabetes and Mild Hyperglycemia
Official Title
A 56-Week Extension to a Clinical Study to Assess the Efficacy and Safety of Vildagliptin Compared to Placebo in Drug Naive Patients With Type 2 Diabetes and Mild Hyperglycemia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
February 20, 2006 (Actual)
Primary Completion Date
June 26, 2007 (Actual)
Study Completion Date
June 26, 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Novartis

4. Oversight

5. Study Description

Brief Summary
This study is not being conducted in the United States. Key long-term clinical studies have shown that people with type 2 diabetes should try to achieve overall blood glucose levels as close to normal as possible. The purpose of this study is to gather data on the long-term safety and effectiveness of vildagliptin, an unapproved drug, compared to placebo in lowering overall blood glucose levels in people with type 2 diabetes who have not been previously treated with drug therapy to lower their blood sugar and whose blood glucose levels are close to normal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
Keywords
Type 2 diabetes, Vildagliptin

7. Study Design

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

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Vildagliptin
Primary Outcome Measure Information:
Title
Change from baseline in HbA1c at 108 weeks
Secondary Outcome Measure Information:
Title
Adverse event profile after 108 weeks of treatment
Title
Change in HbA1c from week 52 to week 108
Title
Change from baseline in fasting plasma glucose at week 108
Title
Change in fasting plasma glucose from week 52 to week 108
Title
Change from baseline in body weight at week 108

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Eligibility Criteria
Inclusion Criteria: Completion of study CLAF237A2307 within 4 weeks of entering into the extension Written informed consent Ability to comply with all study requirements Blood glucose criteria must be met Exclusion Criteria: Premature discontinuation from study CLAF237A2307
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Novartis Pharmaceuticals
Organizational Affiliation
Novartis Pharmaceuticals
Official's Role
Study Director
Facility Information:
City
Investigative Sites
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
18355325
Citation
Scherbaum WA, Schweizer A, Mari A, Nilsson PM, Lalanne G, Wang Y, Dunning BE, Foley JE. Evidence that vildagliptin attenuates deterioration of glycaemic control during 2-year treatment of patients with type 2 diabetes and mild hyperglycaemia. Diabetes Obes Metab. 2008 Nov;10(11):1114-24. doi: 10.1111/j.1463-1326.2008.00875.x. Epub 2008 Mar 18.
Results Reference
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A 56-Week Extension to a Clinical Study to Assess the Efficacy and Safety of Vildagliptin Compared to Placebo in Drug Naive Patients With Type 2 Diabetes and Mild Hyperglycemia

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