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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00333151
Other study ID # NN2211-1574
Secondary ID
Status Completed
Phase Phase 3
First received June 1, 2006
Last updated January 24, 2017
Start date May 2006
Est. completion date August 2007

Study information

Verified date January 2017
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is conducted in the United States of America (USA) and Canada. This trial is designed to show the effect of treatment with liraglutide when added to existing rosiglitazone and metformin combination therapy and to compare it with the effects of therapy with rosiglitazone and metformin alone.


Recruitment information / eligibility

Status Completed
Enrollment 576
Est. completion date August 2007
Est. primary completion date August 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Type 2 diabetes

- Treated with oral anti-diabetic (OAD) drugs for at least 3 months

- Treated with one or more OAD and in moderate to poor glycemic control

- Body Mass Index (BMI) less than or equal to 45.0 kg/m2

Exclusion Criteria:

- Treatment with insulin within the last three months prior to the trial except due to intercurrent illness, at the discretion of the Investigator

- Any serious medical condition

- Treatment with any drug that could interfere with glucose level

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
liraglutide

rosiglitazone

metformin


Locations

Country Name City State
Canada Novo Nordisk Investigational Site Calgary Alberta
Canada Novo Nordisk Investigational Site Edmonton Alberta
Canada Novo Nordisk Investigational Site Gatineau
Canada Novo Nordisk Investigational Site Halifax Nova Scotia
Canada Novo Nordisk Investigational Site Laval Quebec
Canada Novo Nordisk Investigational Site London Ontario
Canada Novo Nordisk Investigational Site Mississauga
Canada Novo Nordisk Investigational Site Montreal
Canada Novo Nordisk Investigational Site Montreal
Canada Novo Nordisk Investigational Site Ottawa Ontario
Canada Novo Nordisk Investigational Site Quebec
Canada Novo Nordisk Investigational Site Red Deer
Canada Novo Nordisk Investigational Site St John's
Canada Novo Nordisk Investigational Site Toronto
Canada Novo Nordisk Investigational Site Toronto Ontario
Canada Novo Nordisk Investigational Site Vancouver
Canada Novo Nordisk Investigational Site Windsor
Canada Novo Nordisk Investigational Site Winnipeg Manitoba
United States Novo Nordisk Investigational Site Albany New York
United States Novo Nordisk Investigational Site Arlington Texas
United States Novo Nordisk Investigational Site Asheville North Carolina
United States Novo Nordisk Investigational Site Athens Georgia
United States Novo Nordisk Investigational Site Atlanta Georgia
United States Novo Nordisk Investigational Site Atlanta Georgia
United States Novo Nordisk Investigational Site Atlanta Georgia
United States Novo Nordisk Investigational Site Baton Rouge Louisiana
United States Novo Nordisk Investigational Site Berlin New Jersey
United States Novo Nordisk Investigational Site Brooklyn New York
United States Novo Nordisk Investigational Site Chapel Hill North Carolina
United States Novo Nordisk Investigational Site Chattanooga Tennessee
United States Novo Nordisk Investigational Site Cincinnati Ohio
United States Novo Nordisk Investigational Site Cleveland Ohio
United States Novo Nordisk Investigational Site Colton California
United States Novo Nordisk Investigational Site Columbus Ohio
United States Novo Nordisk Investigational Site Columbus Ohio
United States Novo Nordisk Investigational Site Concord California
United States Novo Nordisk Investigational Site Dallas Texas
United States Novo Nordisk Investigational Site Dallas Texas
United States Novo Nordisk Investigational Site Dallas Texas
United States Novo Nordisk Investigational Site Dallas Texas
United States Novo Nordisk Investigational Site Dayton Ohio
United States Novo Nordisk Investigational Site Des Moines Iowa
United States Novo Nordisk Investigational Site Duncan South Carolina
United States Novo Nordisk Investigational Site Durham North Carolina
United States Novo Nordisk Investigational Site Escondido California
United States Novo Nordisk Investigational Site Fort Myers Florida
United States Novo Nordisk Investigational Site Goodyear Arizona
United States Novo Nordisk Investigational Site Greenville North Carolina
United States Novo Nordisk Investigational Site Houston Texas
United States Novo Nordisk Investigational Site Houston Texas
United States Novo Nordisk Investigational Site Hyattsville Maryland
United States Novo Nordisk Investigational Site Idaho Falls Idaho
United States Novo Nordisk Investigational Site Jacksonville Florida
United States Novo Nordisk Investigational Site Kettering Ohio
United States Novo Nordisk Investigational Site La Jolla California
United States Novo Nordisk Investigational Site Lake Mary Florida
United States Novo Nordisk Investigational Site Lexington Kentucky
United States Novo Nordisk Investigational Site Long Beach California
United States Novo Nordisk Investigational Site Los Angeles California
United States Novo Nordisk Investigational Site Los Angeles California
United States Novo Nordisk Investigational Site Lubbock Texas
United States Novo Nordisk Investigational Site Mentor Ohio
United States Novo Nordisk Investigational Site Midland Texas
United States Novo Nordisk Investigational Site Milwaukee Wisconsin
United States Novo Nordisk Investigational Site Mission Viejo California
United States Novo Nordisk Investigational Site New Albany Indiana
United States Novo Nordisk Investigational Site New Britain Connecticut
United States Novo Nordisk Investigational Site New Orleans Louisiana
United States Novo Nordisk Investigational Site Newport News Virginia
United States Novo Nordisk Investigational Site Northport New York
United States Novo Nordisk Investigational Site Orange California
United States Novo Nordisk Investigational Site Peoria Illinois
United States Novo Nordisk Investigational Site Plainsboro New Jersey
United States Novo Nordisk Investigational Site Plantation Florida
United States Novo Nordisk Investigational Site Powder Springs Georgia
United States Novo Nordisk Investigational Site Reno Nevada
United States Novo Nordisk Investigational Site Richmond Virginia
United States Novo Nordisk Investigational Site Rochester New York
United States Novo Nordisk Investigational Site Salt Lake City Utah
United States Novo Nordisk Investigational Site San Antonio Texas
United States Novo Nordisk Investigational Site San Antonio Texas
United States Novo Nordisk Investigational Site Santa Ana California
United States Novo Nordisk Investigational Site Santa Barbara California
United States Novo Nordisk Investigational Site Spokane Washington
United States Novo Nordisk Investigational Site Spring Valley California
United States Novo Nordisk Investigational Site St. Louis Missouri
United States Novo Nordisk Investigational Site Topeka Kansas
United States Novo Nordisk Investigational Site Tupelo Mississippi
United States Novo Nordisk Investigational Site Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Countries where clinical trial is conducted

United States,  Canada, 

References & Publications (13)

Alves C, Batel-Marques F, Macedo AF. A meta-analysis of serious adverse events reported with exenatide and liraglutide: acute pancreatitis and cancer. Diabetes Res Clin Pract. 2012 Nov;98(2):271-84. doi: 10.1016/j.diabres.2012.09.008. — View Citation

Blonde L, Russell-Jones D. The safety and efficacy of liraglutide with or without oral antidiabetic drug therapy in type 2 diabetes: an overview of the LEAD 1-5 studies. Diabetes Obes Metab. 2009 Dec;11 Suppl 3:26-34. doi: 10.1111/j.1463-1326.2009.01075.x — View Citation

Bode BW, Brett J, Falahati A, Pratley RE. Comparison of the efficacy and tolerability profile of liraglutide, a once-daily human GLP-1 analog, in patients with type 2 diabetes =65 and <65 years of age: a pooled analysis from phase III studies. Am J Geriat — View Citation

Buse JB, Garber A, Rosenstock J, Schmidt WE, Brett JH, Videbæk N, Holst J, Nauck M. Liraglutide treatment is associated with a low frequency and magnitude of antibody formation with no apparent impact on glycemic response or increased frequency of adverse events: results from the Liraglutide Effect and Action in Diabetes (LEAD) trials. J Clin Endocrinol Metab. 2011 Jun;96(6):1695-702. doi: 10.1210/jc.2010-2822. — View Citation

Davidson JA, Ørsted DD, Campos C. Efficacy and safety of liraglutide, a once-daily human glucagon-like peptide-1 analogue, in Latino/Hispanic patients with type 2 diabetes: post hoc analysis of data from four phase III trials. Diabetes Obes Metab. 2016 Ju — View Citation

Henry RR, Buse JB, Sesti G, Davies MJ, Jensen KH, Brett J, Pratley RE. Efficacy of antihyperglycemic therapies and the influence of baseline hemoglobin A(1C): a meta-analysis of the liraglutide development program. Endocr Pract. 2011 Nov-Dec;17(6):906-13. — View Citation

Jensen TM, Saha K, Steinberg WM. Is there a link between liraglutide and pancreatitis? A post hoc review of pooled and patient-level data from completed liraglutide type 2 diabetes clinical trials. Diabetes Care. 2015 Jun;38(6):1058-66. doi: 10.2337/dc13- — View Citation

King AB, Montanya E, Pratley RE, Blonde L, Svendsen CB, Donsmark M, Sesti G. Liraglutide achieves A1C targets more often than sitagliptin or exenatide when added to metformin in patients with type 2 diabetes and a baseline A1C <8.0%. Endocr Pract. 2013 Ja — View Citation

McGill JB. Insights from the Liraglutide Clinical Development Program--the Liraglutide Effect and Action in Diabetes (LEAD) studies. Postgrad Med. 2009 May;121(3):16-25. doi: 10.3810/pgm.2009.05.1998. Review. — View Citation

Niswender K, Pi-Sunyer X, Buse J, Jensen KH, Toft AD, Russell-Jones D, Zinman B. Weight change with liraglutide and comparator therapies: an analysis of seven phase 3 trials from the liraglutide diabetes development programme. Diabetes Obes Metab. 2013 Ja — View Citation

Sullivan SD, Alfonso-Cristancho R, Conner C, Hammer M, Blonde L. Long-term outcomes in patients with type 2 diabetes receiving glimepiride combined with liraglutide or rosiglitazone. Cardiovasc Diabetol. 2009 Feb 26;8:12. doi: 10.1186/1475-2840-8-12. — View Citation

Zinman B, Gerich J, Buse JB, Lewin A, Schwartz S, Raskin P, Hale PM, Zdravkovic M, Blonde L; LEAD-4 Study Investigators.. Efficacy and safety of the human glucagon-like peptide-1 analog liraglutide in combination with metformin and thiazolidinedione in pa — View Citation

Zinman B, Schmidt WE, Moses A, Lund N, Gough S. Achieving a clinically relevant composite outcome of an HbA1c of <7% without weight gain or hypoglycaemia in type 2 diabetes: a meta-analysis of the liraglutide clinical trial programme. Diabetes Obes Metab. — View Citation

* Note: There are 13 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary HbA1c after 26 weeks of treatment
Secondary body weight
Secondary Safety and tolerability
Secondary Glycaemic control
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