Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting

The ORIGIN Trial (Outcome Reduction With Initial Glargine Intervention) (ORIGIN)

This study has been completed.
Sponsor:
Collaborator:
Population Health Research Institute
Information provided by (Responsible Party):
Sanofi
ClinicalTrials.gov Identifier:
NCT00069784
First received: October 1, 2003
Last updated: January 24, 2013
Last verified: January 2013
Results First Received: December 18, 2012  
Study Type: Interventional
Study Design: Allocation: Randomized;   Endpoint Classification: Efficacy Study;   Intervention Model: Factorial Assignment;   Masking: Open Label;   Primary Purpose: Treatment
Condition: Diabetes Mellitus, Non-Insulin-Dependent
Interventions: Drug: insulin glargine (HOE901)
Drug: omega-3 polyunsaturated fatty acids (PUFA)
Drug: placebo
Device: reusable pen device for insulin injection

  Participant Flow
  Hide Participant Flow

Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
This study was conducted at 575 sites in 40 countries between August 22, 2003 and December 19, 2011. Three sites were closed and data from these sites were not analyzed following site audits and in compliance with rulings from national health authorities.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
The purpose of the factorial design was to efficiently answer two independent scientifically worthwhile questions regarding insulin glargine and omega-3 fatty acids within the context of a single clinical trial. Sample size was determined based on the insulin glargine study objective. Results reported below are those of the insulin glargine study.

Reporting Groups
  Description
Insulin Glargine Treatment with Insulin Glargine with or without omega-3 polyunsaturated fatty acids
Standard Care Standard care with or without omega-3 polyunsaturated fatty acids

Participant Flow:   Overall Study
    Insulin Glargine   Standard Care
STARTED   6264 [1]   6273 [1] 
Safety Population (Treated)   6231 [2]   6273 [3] 
COMPLETED   5052 [4]   6273 [5] 
NOT COMPLETED   1212   0 
Adverse Event                105                0 
Withdrawal by Subject                1090                0 
Other                17                0 
[1] randomized participants = intent-to-treat (ITT) population
[2] randomized patients who received at least one dose of insulin glargine
[3] patients randomized to standard care arm
[4] completed study treatment
[5] not applicable (no treatment)



  Baseline Characteristics
  Hide Baseline Characteristics

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
No text entered.

Reporting Groups
  Description
Insulin Glargine Treatment with Insulin Glargine with or without omega-3 polyunsaturated fatty acids
Standard Care Standard care with or without omega-3 polyunsaturated fatty acids
Total Total of all reporting groups

Baseline Measures
   Insulin Glargine   Standard Care   Total 
Overall Participants Analyzed 
[Units: Participants]
 6264   6273   12537 
Age 
[Units: Years]
Mean (Standard Deviation)
 63.5  (7.8)   63.5  (7.9)   63.5  (7.8) 
Gender, Customized 
[Units: Participants]
     
Male   4181   3969   8150 
Female   2082   2304   4386 
Missing value   1   0   1 
Baseline Weight [1] 
[Units: Kg]
Mean (Standard Deviation)
 83.33  (16.77)   83.13  (17.28)   83.23  (17.03) 
[1] Due to missing values, N=6256 for insulin glargine and N=6271 for standard care.
Baseline Body Mass Index [1] 
[Units: Kg/m²]
Mean (Standard Deviation)
 29.77  (5.17)   29.88  (5.33)   29.82  (5.25) 
[1] Due to missing values, N=6251 for insulin glargine and N=6270 for standard care.
Any previous cardiovascular event 
[Units: Participants]
     
No   2552   2607   5159 
Yes   3712   3666   7378 
Diabetes diagnosis at time of screening [1] 
[Units: Participants]
     
IFG and/or IGT   735   717   1452 
Newly diagnosed diabetic   365   395   760 
Established diabetes with no OAD treatment   1414   1467   2881 
Established diabetes with one OAD treatment   3748   3692   7440 
Unclear diabetes status   2   2   4 
[1]

IFG = Impaired Fasting Glucose defined as a Postprandial Plasma Glucose (PPG) value ≥140 and <200 mg/dL (ie, ≥7.8 and <11.1 mmol/L), with a Fasting Plasma Glucose (FPG) <126 mg/dL (7.0 mmol/L)

IGT = Impaired Glucose Tolerance defined as an FPG ≥110 and <126 mg/dL (≥6.1 and <7 mmol/L), without diabetes mellitus (PPG must be <200 mg/dL [11.1 mmol/L])

OAD = oral antidiabetic drug

Duration of diabetes for established diabetes patients [1] 
[Units: Years]
Median (Inter-Quartile Range)
 3.50 
 (1.50 to 7.50) 
 3.50 
 (1.50 to 7.50) 
 3.50 
 (1.50 to 7.50) 
[1] Population of patients with established diabetes. Due to missing values, N=5148 for insulin glargine and N=5141 for standard care.
Glycated Hemoglobin A1c (HbA1c) [1] 
[Units: Percent]
Median (Inter-Quartile Range)
 6.41 
 (5.81 to 7.18) 
 6.40 
 (5.81 to 7.16) 
 6.40 
 (5.81 to 7.18) 
[1] Due to missing values, N=6175 for insulin glargine and N=6189 for standard care.
Fasting Plasma Glucose [1] 
[Units: mmol/L]
Median (Inter-Quartile Range)
 6.94 
 (6.05 to 8.20) 
 6.90 
 (6.00 to 8.20) 
 6.94 
 (6.05 to 8.20) 
[1] Due to missing values, N=6248 for insulin glargine and N=6266 for standard care.


  Outcome Measures
  Show All Outcome Measures

1.  Primary:   Composite of the First Occurrence of Cardiovascular (CV) Death, Nonfatal Myocardial Infarction (MI) or Nonfatal Stroke   [ Time Frame: from randomization until study cut-off date (median duration of follow-up: 6.2 years) ]
  Hide Outcome Measure 1

Measure Type Primary
Measure Title Composite of the First Occurrence of Cardiovascular (CV) Death, Nonfatal Myocardial Infarction (MI) or Nonfatal Stroke
Measure Description

Number of participants with a first occurrence of one of the above events.

The outcome's evaluation is based on the number of such positively-adjudicated first events occurring for patients assigned to the study groups. Assessments of the above events were reviewed by the Event Adjudication Committee who was kept blinded to the group assignment of participants.

Statistical analysis is performed on the time from randomization to the first occurrence of the events. Number of participants with a composite endpoint (i.e. with first occurrence of CV death, nonfatal MI or nonfatal stroke) is provided in the first row of the statistical table.

Time Frame from randomization until study cut-off date (median duration of follow-up: 6.2 years)  
Safety Issue No  

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.

The analysis was based on the intent-to-treat (ITT) population i.e. all randomized participants.

For the endpoint's composition, the numbers only summarize the event when it was the first occurrence of the endpoint. A participant is counted only once within a category. The same participant may appear in different categories.


Reporting Groups
  Description
Insulin Glargine Treatment with Insulin Glargine with or without omega-3 polyunsaturated fatty acids
Standard Care Standard care with or without omega-3 polyunsaturated fatty acids

Measured Values
   Insulin Glargine   Standard Care 
Participants Analyzed 
[Units: Participants]
 6264   6273 
Composite of the First Occurrence of Cardiovascular (CV) Death, Nonfatal Myocardial Infarction (MI) or Nonfatal Stroke 
[Units: Participants]
   
Participants with a composite endpoint   1041   1013 
Endpoint's composition: CV death   484   476 
Endpoint's composition: nonfatal MI   297   282 
Endpoint's composition: nonfatal stroke   261   256 


Statistical Analysis 1 for Composite of the First Occurrence of Cardiovascular (CV) Death, Nonfatal Myocardial Infarction (MI) or Nonfatal Stroke
Groups [1] All groups
Method [2] Log Rank
P Value [3] 0.6273
Cox Proportional Hazard [4] 1.022
95% Confidence Interval 0.937 to 1.114
[1] Additional details about the analysis, such as null hypothesis and power calculation:
  The total required number of first coprimary outcomes (2200) assumed that a hazard reduction of 14-16% was clinically significant and controlled the overall experiment-wise Type 1 error at 5% with a power of 80% for each outcome. The total number of participants needed to achieve this number of events within the planned enrollment and treatment periods was ultimately estimated to be 12 500 based on the CURE and HOPE study databases.
[2] Other relevant method information, such as adjustments or degrees of freedom:
  Log-rank test stratified by double-blind treatment (omega-3 PUFA, placebo), baseline diabetes diagnosis and previous CV event.
[3] Additional information, such as whether or not the p-value is adjusted for multiple comparisons and the a priori threshold for statistical significance:
  For the analysis of the two coprimary efficacy outcomes, the overall Type 1 error was partitioned. The first coprimary outcome was tested at 4.4%, whereas the second coprimary outcome was tested at 1% (weighted Hochberg procedure).
[4] Other relevant estimation information:
  Hazard ratio (glargine/standard care) estimated by Cox regression model with treatment (glargine, standard care) as factor, stratified by double-blind treatment (omega-3 PUFA, placebo), baseline diabetes diagnosis and previous CV event.



2.  Primary:   Composite of the First Occurrence of Cardiovascular (CV) Death, Nonfatal Myocardial Infarction (MI), Nonfatal Stroke, Revascularization Procedure or Hospitalization for Heart Failure (HF)   [ Time Frame: from randomization until study cut-off date (median duration of follow-up: 6.2 years) ]

3.  Secondary:   Total Mortality (All Causes)   [ Time Frame: from randomization until study cut-off date (median duration of follow-up: 6.2 years) ]

4.  Secondary:   Composite Diabetic Microvascular Outcome (Kidney or Eye Disease)   [ Time Frame: from randomization until study cut-off date (median duration of follow-up: 6.2 years) ]

5.  Secondary:   Incidence of Development of Type 2 Diabetes Mellitus in Participants With IGT and/or IFG   [ Time Frame: from randomization until the last follow-up visit or last OGTT (median duration of follow-up: 6.2 years) ]

6.  Other Pre-specified:   Number of Patients With Various Types of Symptomatic Hypoglycemia Events   [ Time Frame: on-treatment period (median duration of follow-up: 6.2 years) ]
  Hide Outcome Measure 6

Measure Type Other Pre-specified
Measure Title Number of Patients With Various Types of Symptomatic Hypoglycemia Events
Measure Description

Symptomatic hypoglycemia was defined as an event with clinical symptoms consistent with hypoglycemia, based on data recorded in the participant’s diary. These were further categorized as confirmed (ie, with a concomitant home glucose reading ≤54 mg/dL [≤3.0 mmol/L]) or unconfirmed.

Severe hypoglycemia was defined as an event with clinical symptoms consistent with hypoglycemia in which the participant required the assistance of another person, and one of the following:

  • the event was associated with a documented self-measured or laboratory plasma glucose level ≤36 mg/dL (≤2.0 mmol/L), or
  • the event was associated with prompt recovery after oral carbohydrate, intravenous glucose, or glucagon administration.
Time Frame on-treatment period (median duration of follow-up: 6.2 years)  
Safety Issue Yes  

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
The population analyzed was the safety population consisting of all randomized and treated patients (who received at least one dose of study drug) for the insulin glargine group and of all randomized patients for the standard care group.

Reporting Groups
  Description
Insulin Glargine Treatment with Insulin Glargine with or without omega-3 polyunsaturated fatty acids
Standard Care Standard care with or without omega-3 polyunsaturated fatty acids

Measured Values
   Insulin Glargine   Standard Care 
Participants Analyzed 
[Units: Participants]
 6231   6273 
Number of Patients With Various Types of Symptomatic Hypoglycemia Events 
[Units: Participants]
   
Patients with hypoglycemia events   3597   1624 
Patients with non-severe hypoglycemia   3533   1582 
Patients with confirmed non-severe hypoglycemia   2581   904 
Patients with severe hypoglycemia   352   113 

No statistical analysis provided for Number of Patients With Various Types of Symptomatic Hypoglycemia Events



7.  Other Pre-specified:   Number of Patients With First Occurrence of Any Type of Cancer   [ Time Frame: from randomization until study cut-off date (median duration of follow-up: 6.2 years) ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
  Hide Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
No text entered.


  More Information