Linagliptin in Combination With Metformin in Treatment Naive Patients With Type 2 Diabetes Mellitus and Insufficient Glycaemic Control

This study has been completed.
Sponsor:
Collaborator:
Eli Lilly and Company
Information provided by (Responsible Party):
Boehringer Ingelheim
ClinicalTrials.gov Identifier:
NCT01438814
First received: September 21, 2011
Last updated: July 24, 2013
Last verified: July 2013

September 21, 2011
July 24, 2013
November 2011
March 2013   (final data collection date for primary outcome measure)
The change from baseline in Glycosylated Hemoglobin A1c (HbA1c) after 14 weeks treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01438814 on ClinicalTrials.gov Archive Site
  • Occurence of metformin pre-specified moderate to severe GI side effects assessed by investigators during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Occurrence of relative efficacy response (HbA1c lowering by at least 0.8% after 14 weeks of treatment) [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endpoint of occurence of relative efficacy response(HbA1c lowering by at least 0.5% after 14 weeks of treatment) and no occurence of moderate and severe metformin pre-specified GI side effects assessed by the investigators during 14 weeks [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endpoint of occurrence of relative efficacy response(HbA1c lowering by at least 0.8% after 14 weeks of treatment) and no occurrence of moderate and severe metformin pre-specified GI side effects assessed by investigators during 14 weeks [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • change from baseline in HbA1c by visit over time [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • change from baseline in body weight by visit over time [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endpoint of occurence of treat to target efficacy response, that is an HbA1c under treatment of <7.0% after 14 weeks of treatment, and no occurence of moderate or severe gastrointestinal (GI) side effects during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Change from baseline in fasting plasma glucose (FPG) after 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Metformin pre-specified GI symptom intensity score assessed by investigators during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Metformin pre-specified GI symptom intensity score assessed by patients during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endpoint of occurrence of treat to target efficacy response, that is an HbA1c under treatment of <6.5% after 14 weeks of treatment, and on occurence of moderate or severe metformin pre-specified GI side effects assessed by investigators [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Occurrence of relative efficacy response (HbA1c lowering by at least 0.5% after 14 weeks of treatment) [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Occurence of metformin pre-specified moderate to severe GI side effects assessed by investigators during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Occurrence of relative efficacy response (HbA1c lowering by at least 0.8% after 14 weeks of treatment) [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endponit of occurence of relative efficacy response(HbA1c lowering by at least 0.5% after 14 weeks of treatment) and no occurence of moderate and severe metformin pre-specified GI side effects assessed by the investigators during 14 weeks [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Compostie endpoint of occurrence of relative efficacy response(HbA1c lowering by at least 0.8% after 14 weeks of treatment) and no occurrence of moderate and severe metformin pre-specified GI side effects assessed by investigators during 14 weeks [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • change from baseline in HbA1c by visit over time [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • change from baseline in body weight by visit over time [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endpoint of occurence of treat to target efficacy response, that is an HbA1c under treatment of <7.0% after 14 weeks of treatment, and no occurence of moderate or severe gastrointestinal (GI) side effects during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Change from baseline in fasting plasma glucose (FPG) after 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Metformin pre-specified GI symptom intensity score assessed by investigators during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Metformin pre-specified GI symptom intensty score assessed by patients during 14 weeks of treatment [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Composite endpoint of occurrence of treat to target efficacy response, that is an HbA1c under treatment of <6.5% after 14 weeks of treatment, and on occurence of moderate or severe metformin pre-specified GI side effects assessed by investigators [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
  • Occurrence of relative efficacy response (HbA1c lowering by at least 0.5% after 14 weeks of treatment) [ Time Frame: 14 weeks ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Linagliptin in Combination With Metformin in Treatment Naive Patients With Type 2 Diabetes Mellitus and Insufficient Glycaemic Control
A Randomised, Double-blind, Double-dummy, Active-comparator Controlled Study Investigating the Efficacy and Safety of Linagliptin Co-administered With Metformin QD at Evening Time Versus Metformin BID Over 14 Weeks in Treatment Naive Patients With Type 2 Diabetes Mellitus and Insufficient Glycaemic Control

This phase IV, randomized, double-blind, double-dummy, active-comparator controlled study is to compare the efficacy and safety of linagliptin (5mg) co-administered with metformin (QD, metformin daily dose 1000mg)at evening time with metformin BID (min daily dose 1000mg, max.daily dose 2000mg) over 14 weeks in treatment naive patients with type 2 diabetes mellitus and insufficient glycaemic control.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Diabetes Mellitus, Type 2
  • Drug: metformin placebo
    metformin placebo tablets 500mg
  • Drug: linagliptin placebo
    linagliptin placebo tablets 5mg
  • Drug: metformin
    metformin tablets 500mg
  • Drug: placebo metformin
    placebo metformin 500 mg
  • Drug: metformin
    metformin tablets 500 mg
  • Drug: linagliptin
    linaglitpin tablets 5mg
  • Experimental: linagliptin + metformin
    patients to receive lingliptin +metformin QD
    Interventions:
    • Drug: placebo metformin
    • Drug: metformin
    • Drug: linagliptin
  • Active Comparator: metformin
    patients to receive metformin BID
    Interventions:
    • Drug: metformin placebo
    • Drug: linagliptin placebo
    • Drug: metformin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
689
March 2013
March 2013   (final data collection date for primary outcome measure)

Inclusion criteria:

  1. Diagnosis of Type 2 diabetes mellitus (T2DM) prior to informed consent;
  2. Male and female patients on diet and exercise regimen who are drug naive, defined as absence of any oral antidiabetic therapy or insulin for 12 weeks prior to randomization
  3. Glycosylated haemoglobin A1c (HbA1c) >/= 7.0% (53 mmol/mol) to </= 10.0% (86 mmol/mol)at visit 1 (screening);
  4. Age>/=18 and </=80 years at visit 1(screening);
  5. Body Mass Index(BMI)</= 45kg/m2 at vist 1 (screening);
  6. Signed and dated written informed consent by date of visit 1 in accordance with Good Clinical Practice (GCP) and local legislation

Exclusion criteria:

  1. Uncontrolled hyperglycaemia with a glucose level >240 mg/dl (13.3mmol/L) after an overnight fast during screening/placebo run-in and confirmed by a second measurement (Not on the same day);
  2. Treatment with any oral antidiabetic drug or insulin within 12 weeks prior to randomization
  3. Myocardial infarction,stroke or Transient ischemia attack (TIA) within 3 months prior to informed consent;
  4. Indication of liver disease/Impaired hepatic function, defined by serum levels of either Aspartate aminotransferase (ALT or SGPT), alanine aminotransferase (AST or SGOT), or alkaline phosphatase above 3 x upper limit of normal (ULN) as determined at visit 1,
  5. Impaired renal function, defined as eGFR< 60ml/min (severe renal impairment, modification of diet in renal disease (MDRD) formula) as determined at run-in phase
  6. Bariatric surgery within the past two years and other gastrointestinal surgeries that induced chronic malabsorption
  7. Medical history of Cancer(except for basal cell carcinoma) and/or treatment for cancer within the last 5 years
  8. Blood dyscrasia or any other disorders causing haemolysis or unstable Red Blood Cell (eg. malaria, babesiosis, haemolytic anemia)
  9. Known history of pancreatitis and chronic pancreatitis
  10. Contraindications to metformin according to the local label
  11. Treatment with anti-obesity drugs 3 months prior to informed consent or any other treatment at the time of screening (i.e. surgery, aggressive diet regimen etc) leading to unstable body weight
  12. Current treatment with systemic steroids at time of informed consent or change in dosage of thyroid hormones within 6 weeks prior to informed consent or any other uncontrolled endocrine disorder except T2DM
  13. Pre-menopausal women (last menstruation less than 1 year prior to informed consent) who:

    1. are nursing or pregnant or
    2. are of child-bearing potential and are not practicing an acceptable method of birth control, or do not plan to continue using this method throughout the study and do not agree to submit to periodic pregnancy testing during participation in the trial or who do not agree to continue contraception for at least 30 days after the last dose of study drug. Acceptable methods of birth control include transdermal patch, intra-uterine devices/systems (IUDs/IUSs), oral, implantable or injectable contraceptives, sexual abstinence and vasectomised partner.
  14. Alcohol or drug abuse within 3 months prior to informed consent that would interfere with trial participation or any ongoing condition leading to a decreased compliance to study procedures or study drgu intake
  15. Participation in another trial with application of any investigational drug within 30 days prior to informed consent
  16. Any other clinical condition that would jeopardize patients safety while participating in this trial
Both
18 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
Bangladesh,   Belgium,   Canada,   China,   Germany,   Guatemala,   Hong Kong,   India,   Lebanon,   Mexico,   Peru,   Philippines,   Spain,   Taiwan
 
NCT01438814
1218.60, 2011-002276-16
Not Provided
Boehringer Ingelheim
Boehringer Ingelheim
Eli Lilly and Company
Study Chair: Boehringer Ingelheim Boehringer Ingelheim
Boehringer Ingelheim
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP