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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01159249
Other study ID # CLAF237A1308
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date June 2010
Est. completion date January 2012

Study information

Verified date May 2012
Source Novartis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to demonstrate the long-term safety of vildagliptin in patients with type 2 diabetes. This study will study vildagliptin as add-on therapy with metformin, thiazolidinedione, α-glucosidase inhibitor (α-GI), rapid-acting insulin secretagogues in the treatment of type 2 diabetes in Japan.


Recruitment information / eligibility

Status Completed
Enrollment 245
Est. completion date January 2012
Est. primary completion date January 2012
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - patients with type 2 diabetes inadequately controlled with diet, exercise and metformin, thiazolidinedione, or a-GI, or glinides monotherapy - Age in the 20 years or over inclusive - HbA1c in the range of = 6.5 to = 10% Exclusion Criteria: - Type 1 diabetes mellitus, diabetes that is a result of pancreatic injury, or secondary forms of diabetes - Significant heart diseases - Significant diabetic complications

Study Design


Intervention

Drug:
Vildagliptin


Locations

Country Name City State
Japan Novartis Investigative Site Chikushino Fukuoka
Japan Novartis Investigative Site Edogawa-ku Tokyo
Japan Novartis Investigative Site Fukuoka
Japan Novartis Investigative Site Fukuoka
Japan Novartis Investigative Site Fukuoka
Japan Novartis Investigative Site Hachioji Tokyo
Japan Novartis Investigative Site Hannou Saitama
Japan Novartis Investigative Site Hiki-Gun Saitama
Japan Novartis Investigative Site Hunabashi Chiba
Japan Novartis Investigative Site Itoshima-shi Fukuoka
Japan Novartis Investigative Site Izumisano Osaka
Japan Novartis Investigative Site Katsushika-ku Tokyo
Japan Novartis Investigative Site Kawaguchi Saitama
Japan Novartis Investigative Site Kawasaki Kanagawa
Japan Novartis Investigative Site Kawasaki Kanagawa
Japan Novartis Investigative Site Kobe Hyogo
Japan Novartis Investigative Site Koriyama Fukushima
Japan Novartis Investigative Site Koshigaya city Saitama
Japan Novartis Investigative Site Minato-ku Tokyo
Japan Novartis Investigative Site Shinagawa-ku Tokyo
Japan Novartis Investigative Site Tokorozawa Saitama
Japan Novartis Investigative Site Toshima-ku Tokyo
Japan Novartis Investigative Site Yokohama Kanagawa
Japan Novartis Investigative Site Yokohama-city Kanagawa

Sponsors (1)

Lead Sponsor Collaborator
Novartis Pharmaceuticals

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure AEs, vital signs, laboratory evaluations 52 weeks
Secondary HBA1c 52 weeks
Secondary Fasting Plasma Glucose 52 weeks
Secondary Fasting Insulin 52 weeks
Secondary Fasting C-peptide 52 weeks
Secondary HOMA-B 52 weeks
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