Efficacy and Safety of FIAsp Compared to Insulin Aspart in Combination With Insulin Glargine and Metformin in Adults With Type 2 Diabetes (onset® 2)

This study is currently recruiting participants.
Verified February 2014 by Novo Nordisk A/S
Sponsor:
Information provided by (Responsible Party):
Novo Nordisk A/S
ClinicalTrials.gov Identifier:
NCT01819129
First received: March 21, 2013
Last updated: February 19, 2014
Last verified: February 2014
  Purpose

This trial is conducted in Asia, Europe and North America. The aim of the trial is to compare FIAsp (faster-acting insulin aspart) to insulin aspart, both in combination with insulin glargine and metformin in adults with type 2 diabetes.


Condition Intervention Phase
Diabetes
Diabetes Mellitus, Type 2
Drug: insulin aspart (FIAsp)
Drug: insulin aspart
Drug: insulin glargine
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: Efficacy and Safety of FIAsp Compared to Insulin Aspart in Combination With Insulin Glargine and Metformin in Adults With Type 2 Diabetes

Resource links provided by NLM:


Further study details as provided by Novo Nordisk A/S:

Primary Outcome Measures:
  • Change from baseline in HbA1c [ Time Frame: Week 0, week 26 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Change from baseline in 2-hour PPG increment (meal test) [ Time Frame: Week 0, week 26 ] [ Designated as safety issue: No ]
  • Number of treatment emergent confirmed hypoglycaemic episodes [ Time Frame: From week 0 to week 26 ] [ Designated as safety issue: No ]
  • Change from baseline in body weight [ Time Frame: Week 0, week 26 ] [ Designated as safety issue: No ]

Estimated Enrollment: 676
Study Start Date: September 2013
Estimated Study Completion Date: January 2015
Estimated Primary Completion Date: January 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Insulin aspart (FIAsp) Drug: insulin aspart (FIAsp)
Mealtime FIAsp administered subcutaneously (s.c., under the skin). Dose individually adjusted.
Drug: insulin glargine
Administered s.c. once daily at subjects' pre-trial dose. Subjects will continue their metformin treatment without changing the frequency or dose throughout the trial.
Active Comparator: Insulin aspart Drug: insulin aspart
Mealtime insulin aspart administered subcutaneously (s.c., under the skin). Dose individually adjusted.
Drug: insulin glargine
Administered s.c. once daily at subjects' pre-trial dose. Subjects will continue their metformin treatment without changing the frequency or dose throughout the trial.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Type 2 diabetes (diagnosed clinically) for 6 months or longer at time of screening (visit 1)
  • Treated with basal insulin for at least 6 months prior to screening (visit 1)
  • Current once daily treatment with insulin NPH (Neutral Protamine Hagedorn), insulin detemir or glargine for at least 3 months prior to the screening visit (visit 1)
  • Current treatment with: a. metformin with unchanged dosing for at least 3 months prior to screening (visit 1). The metformin dose must be at least 1000 mg or b. metformin in combination with sulfonylurea (SU) or glinide or DPP-IV (dipeptidyl peptidase-4) inhibitors and/or alpha-glucosidase inhibitors (AGI) with unchanged dosing for at least 3 months prior to screening (visit 1). The metformin dose must be at least 1000 mg
  • HbA1c by central laboratory: a. 7.0 - 9.5% (53 - 80 mmol/mol) (both inclusive) in the metformin group at the screening visit (visit 1) or b. 7.0 - 9.0% (53 - 75 mmol/mol) (both inclusive) in the metformin + other OAD (oral antidiabetic drug) (SU, glinide, DDP-IV inhibitors, AGI) combination group at the screening visit (visit 1)
  • Body mass index (BMI) equal to or below 40.0 kg/m^2

Exclusion Criteria:

  • Any use of bolus insulin, except short-term use due to intermittent illness (no longer than 14 days consecutive treatment) and not 3 months prior to the screening visit (visit 1)
  • Use of GLP-1 (glucagon-like peptide-1) agonists and/or TZDs within the last 3 months prior to screening (visit 1)
  • Recurrent severe hypoglycaemia (more than 1 severe hypoglycaemic event during the last 12 months) or hypoglycaemic unawareness as judged by the Investigator or hospitalisation for diabetic ketoacidosis during the previous 6 months prior to screening (visit 1)
  • Cardiovascular disease, within the last 6 months prior to screening (visit 1), defined as: stroke, decompensated heart failure New York Heart Association (NYHA) class III or IV, myocardial infarction, unstable angina pectoris or coronary arterial bypass graft or angioplasty
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01819129

Contacts
Contact: Novo Nordisk clinicaltrials@novonordisk.com

  Hide Study Locations
Locations
United States, Arizona
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Glendale, Arizona, United States, 85308
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Glendale, Arizona, United States, 85306-4652
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Mesa, Arizona, United States, 85213
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Phoenix, Arizona, United States, 85020
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Tempe, Arizona, United States, 85283
United States, California
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Anaheim, California, United States, 92801
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Fresno, California, United States, 93720
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Greenbrae, California, United States, 94904
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Lomita, California, United States, 90717
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Northridge, California, United States, 91325
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San Diego, California, United States, 92111
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San Ramon, California, United States, 94583
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Walnut Creek, California, United States, 94598
United States, Colorado
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Aurora, Colorado, United States, 80045
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Colorado Springs, Colorado, United States, 80910
United States, Connecticut
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Waterbury, Connecticut, United States, 06708
United States, Florida
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Boynton Beach, Florida, United States, 33472
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Bradenton, Florida, United States, 34208
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Cooper City, Florida, United States, 33024
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Fort Lauderdale, Florida, United States, 33316-2521
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Jacksonville, Florida, United States, 32216
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Jacksonville, Florida, United States, 32205
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Miami, Florida, United States, 33144
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Miami, Florida, United States, 33173
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Pembroke Pines, Florida, United States, 33027
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Tampa, Florida, United States, 33603
United States, Georgia
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Atlanta, Georgia, United States, 30308-2253
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Roswell, Georgia, United States, 30076
United States, Illinois
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Peoria, Illinois, United States, 61602
United States, Indiana
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Avon, Indiana, United States, 46123
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Indianapolis, Indiana, United States, 46254
United States, Kansas
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Topeka, Kansas, United States, 66606
United States, Kentucky
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Louisville, Kentucky, United States, 40206
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Madisonville, Kentucky, United States, 42431-1661
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Paducah, Kentucky, United States, 42003
United States, Louisiana
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Monroe, Louisiana, United States, 71203
United States, Michigan
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Buckley, Michigan, United States, 49620
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Detroit, Michigan, United States, 48201
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Troy, Michigan, United States, 48085-5524
United States, Missouri
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Chesterfield, Missouri, United States, 63017
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Jefferson City, Missouri, United States, 65109-6001
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St. Louis, Missouri, United States, 63141
United States, Montana
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Butte, Montana, United States, 59701
United States, Nebraska
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Elkhorn, Nebraska, United States, 68022
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Omaha, Nebraska, United States, 68105
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Omaha, Nebraska, United States, 68198-3020
United States, New Jersey
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Toms River, New Jersey, United States, 08755-8050
United States, New York
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Mineola, New York, United States, 11501
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New Windsor, New York, United States, 12553
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North Massapequa, New York, United States, 11758-1802
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Northport, New York, United States, 11768
United States, North Carolina
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Hickory, North Carolina, United States, 28602
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Wilmington, North Carolina, United States, 28401
United States, Ohio
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Carlisle, Ohio, United States, 45005
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Cleveland, Ohio, United States, 44122
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Dayton, Ohio, United States, 45439
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Franklin, Ohio, United States, 45005
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Mason, Ohio, United States, 45040-6815
United States, Rhode Island
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East Providence, Rhode Island, United States, 02914
United States, South Carolina
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Gaffney, South Carolina, United States, 29341
United States, Tennessee
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Chattanooga, Tennessee, United States, 37404
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Johnson City, Tennessee, United States, 37604
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Spring Hill, Tennessee, United States, 37174
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Tullahoma, Tennessee, United States, 37388
United States, Texas
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Dallas, Texas, United States, 75251
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Dallas, Texas, United States, 75230
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Hurst, Texas, United States, 76054
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Plano, Texas, United States, 75075
United States, Utah
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Murray, Utah, United States, 84123
United States, Virginia
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Midlothian, Virginia, United States, 23114
United States, Washington
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Port Orchard, Washington, United States, 98366
United States, Wisconsin
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Kenosha, Wisconsin, United States, 53142-7884
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Milwaukee, Wisconsin, United States, 53209
Canada, British Columbia
Recruiting
Surrey, British Columbia, Canada, V3S 2N6
Croatia
Recruiting
Osijek, Croatia, 31 000
India
Recruiting
Indore, Madhya Pradesh, India, 452010
Israel
Recruiting
Beer Sheva, Israel, 84101
Puerto Rico
Novo Nordisk Clinical Trial Call Center Recruiting
Ponce, Puerto Rico, 00717
Russian Federation
Recruiting
Saint-Petersburg, Russian Federation, 194358
Serbia
Recruiting
Belgrade, Serbia, 11000
Slovakia
Recruiting
Bratislava, Slovakia, 851 01
United Kingdom
Recruiting
Stoke on Trent, United Kingdom, ST4 6QG
Sponsors and Collaborators
Novo Nordisk A/S
Investigators
Study Director: Kit Gjølbye Madsen Novo Nordisk A/S
  More Information

Additional Information:
No publications provided

Responsible Party: Novo Nordisk A/S
ClinicalTrials.gov Identifier: NCT01819129     History of Changes
Other Study ID Numbers: NN1218-3853, U1111-1118-2509, CTRI/2014/01/004285
Study First Received: March 21, 2013
Last Updated: February 19, 2014
Health Authority: Canada: Health Canada
Croatia: Ministry of Health and Social Care
India: Drugs Controller General of India
Israel: Ministry of Health
Russia: Ministry of Health of the Russian Federation
Serbia: Agency for Drugs and Medicinal Devices
Slovakia: State Institute for Drug Control
United Kingdom: Medicines and Healthcare Products Regulatory Agency
United States: Food and Drug Administration

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Insulin aspart
Glargine
Insulin
Metformin
Insulin, Long-Acting
Hypoglycemic Agents
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on April 17, 2014