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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00349128
Other study ID # C LF23-0121 03 01
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received July 5, 2006
Last updated August 31, 2007
Start date January 2004

Study information

Verified date August 2007
Source Solvay Pharmaceuticals
Contact n/a
Is FDA regulated No
Health authority Ukraine: State Pharmacological Center - Ministry of HealthPoland: Ministry of HealthFrance: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

The primary objective was to assess the effect of 3-month treatment of low and standard doses of fenofibrate in combination with stable dose of metformin on fasting triglycerides levels in patients with type 2 diabetes and dyslipidemia.


Recruitment information / eligibility

Status Completed
Enrollment 382
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Type 2 diabetes mellitus

Exclusion Criteria:

- Type 1 diabetes, uncontrolled type 2 diabetes, - HbA1c = 10 % - Fasting plasma glucose > 300 mg/dL - Triglycerides > 500 mg/dL

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
fenofibrate and metformin combination (drug)


Locations

Country Name City State
Poland Site 201 Katowice
Poland Site 203 Katowice
Poland Site 202 Warszawa
Poland Site 204 Zabrze
Ukraine Site 111 Dnipropetrovsk
Ukraine Site 113 Dnipropetrovsk
Ukraine Site 108 Kharkiv
Ukraine Site 109 Kharkiv
Ukraine Site 101 Kyiv
Ukraine Site 102 Kyiv
Ukraine Site 103 Kyiv
Ukraine Site 104 Kyiv
Ukraine Site 105 Kyiv
Ukraine Site 106 Kyiv
Ukraine Site 107 Kyiv
Ukraine Site 112 Zaporizhya
United Kingdom Site 35 Acomb
United Kingdom Site 21 Atherstone
United Kingdom Site 14 Balsall Common
United Kingdom Site 32 Bangor
United Kingdom Site 23 Barry
United Kingdom Site 36 Basingstoke
United Kingdom Site 8 Bexhill-on-Sea
United Kingdom Site 20 Camberley
United Kingdom Site 22 Chesterfield
United Kingdom Site 10 Chippenham
United Kingdom Site 13 Coventry
United Kingdom Site 31 Doncaster
United Kingdom Site 15 Downpatrick
United Kingdom Site 17 Ely
United Kingdom Site 4 Ely
United Kingdom Site 11 Fife
United Kingdom Site 1 Frome
United Kingdom Site 16 Harrow
United Kingdom Site 5 Hastings
United Kingdom Site 26 Haverfordwest
United Kingdom Site 19 Keresley end
United Kingdom Site 9 Kingswood
United Kingdom Site 25 Newtownabbey
United Kingdom Site 33 Northampton
United Kingdom Site 28 Odiham
United Kingdom Site 3 Paignton
United Kingdom Site 12 Petersborough
United Kingdom Site 7 Randalstown
United Kingdom Site 27 Slough
United Kingdom Site 6 Soham
United Kingdom Site 2 South Glamorgan
United Kingdom Site 34 Stratford on Avon
United Kingdom Site 29 Swindon
United Kingdom Site 30 Trowbridge
United Kingdom Site 18 Yaxley

Sponsors (1)

Lead Sponsor Collaborator
Solvay Pharmaceuticals

Countries where clinical trial is conducted

Poland,  Ukraine,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in fasting triglycerides.
Secondary Assessment of lipid and glucose metabolisms.
See also
  Status Clinical Trial Phase
Completed NCT00362323 - Fenofibrate and Metformin Fixed Combination vs Metformin - FAME METFO Phase 3
Completed NCT00348725 - Acceptability of a Fixed Combination of Fenofibrate and Metformin Phase 3