Skip to content

The LANCET Trial: A Trial of Long-acting Insulin Injection to Reduce C-reactive Protein in Patients With Type 2 Diabetes

The LANCET Trial: A Randomized Clinical Trial of Lantus for C-reactive Protein Reduction in Early Treatment of Type 2 Diabetes

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00366301
Enrollment
500
Registered
2006-08-21
Start date
2006-08-31
Completion date
2009-04-30
Last updated
2010-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Keywords

type 2 diabetes, insulin, insulin injection, metformin, C-reactive protein, insulin sensitivity, glycemic control, inflammation

Brief summary

The purpose of this study, which is being conducted at 100 centers throughout the United States, is to determine whether Lantus, a long-acting insulin injection, either alone or in combination with metformin, is effective in reducing C-reactive protein (CRP) in adults with type 2 diabetes. CRP is a marker of chronic low-level inflammation, a new risk factor for diabetes, heart attack, stroke, and other cardiovascular events.

Detailed description

Study Rationale Low-grade systemic inflammation as indicated by elevated levels of C-reactive protein (CRP) is often present in patients with type 2 diabetes. Individuals with type 2 diabetes represent a vulnerable population in which cardiovascular event rates are high and among whom CRP reduction may have the greatest impact. While several classes of oral hypoglycemic agents have been shown to lower CRP, data are not available for newer formulations of long-acting insulins such as Lantus (insulin glargine injection) and no study has comprehensively evaluated the relative merit of insulin-providing versus insulin-sensitizing strategies for this purpose. Investigational Plan This is a multicenter, community-based, randomized 2x2 factorial trial of Lantus and metformin among patients with type 2 diabetes treated with either diet or oral monotherapy (other than metformin) only who have poor glycemic control and elevated CRP. The primary endpoint is change in CRP. Secondary endpoints include improvement in insulin sensitivity, glycemic control, blood lipids, as well as selected inflammatory and prothrombotic markers, and adipokine levels. Limited data suggest that short-term insulin administration in patients with poorly controlled type 2 diabetes may lower CRP, but the benefit of CRP reduction that is unique to insulin therapy and independent of glycemic control per se remains uncertain. The insulin-sensitizing agent metformin, a mainstay of anti-diabetic therapy, has been shown to reduce macrovascular complications among patients with type 2 diabetes and, in some but not all randomized clinical trials, also has a modest CRP-lowering effect. This study is designed to assess whether the use of Lantus either alone or in combination with metformin lowers CRP over a 14-week treatment period. Eligible men and women age 18 to 79 years with early diabetes on diet only or oral monotherapy with baseline HbA1c 7.0-10% and CRP greater than or equal to 2.0 mg/l will be randomized in a 2X2 factorial fashion as follows. First, participants will be assigned at random to open-label Lantus or no insulin. Then, within these two categories, subjects will be assigned at random to metformin or placebo. Thus, the four resultant treatment groups are Lantus injection and placebo pill, Lantus injection and metformin pill, metformin pill alone, and placebo pill alone. All patients will receive diet and exercise counseling. This study design will permit testing of the overall effect of Lantus as well as the effect of combination therapy with metformin for CRP reduction at a targeted level of glycemic control (fingerstick fasting blood glucose \< 110 mg/dl). All participants will be provided with a glucometer for fingerstick glucose testing calibrated to report plasma-referenced values.

Interventions

DRUGInsulin glargine injection

Once daily for 14 weeks

DRUGmetformin

Up to 4 pils per day (2g per day) maximum

DRUGPlacebo pill

Up to 4 pills per day

Sponsors

Sanofi
CollaboratorINDUSTRY
Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
No

Inclusion criteria

* Men and women aged 18 to 79 * Type 2 diabetes, treated only by diet or oral drugs other than metformin * HbA1c greater than or equal to 7% and less than or equal to 10% * C-reactive protein greater than or equal to 2 mg/L

Exclusion criteria

* Baseline use of metformin or insulin * Type 1 diabetes, history of ketoacidosis or positive anti-GAD antibody * History of congestive heart failure requiring drug therapy * Active liver disease * Kidney impairment * Recent initiation or change in dose of statins, fibric acid derivatives, angiotensin receptor blockers, nonsteroidal anti-inflammatory agents, or corticosteroids

Design outcomes

Primary

MeasureTime frame
Percentage Reduction in C-reactive Protein (CRP)14 weeks

Countries

United States

Participant flow

Recruitment details

Recruitment occurred at 73 US office-based practices between October 2006 and December 2008.

Pre-assignment details

Preenrollment evaluation comprised local laboratory testing of hsCRP,HbA1c, and safety parameters (ALT or AST and creatinine). Eligible participants were enrolled in a 2-week run-in. Ability to self-monitor fingerstick blood glucose and perform insulin injection was determined and evaluation for evidence of marked hyperglycemia was undertaken.

Participants by arm

ArmCount
Placebo Pill
Placebo pill
124
Metformin Pill
Metformin pill
126
Insulin Glargine Plus Placebo Pill
Insulin glargine plus placebo pill
126
Insulin Glargine Plus Metformin Pill
Insulin Glargine plus metformin pill
124
Total500

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003
Overall StudyLost to Follow-up4437
Overall StudyWithdrawal by Subject4211

Baseline characteristics

CharacteristicPlacebo PillTotalInsulin Glargine Plus Metformin PillInsulin Glargine Plus Placebo PillMetformin Pill
Age Continuous
Mean (SD)
54.0 years
STANDARD_DEVIATION 10.9
53.9 years
STANDARD_DEVIATION 11.4
54.0 years
STANDARD_DEVIATION 11.7
53.8 years
STANDARD_DEVIATION 11.4
53.8 years
STANDARD_DEVIATION 11.5
Ethnicity (NIH/OMB)
Hispanic or Latino
13 Participants53 Participants17 Participants19 Participants4 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
110 Participants438 Participants105 Participants104 Participants119 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
1 Participants9 Participants2 Participants3 Participants3 Participants
Race/Ethnicity, Customized
African American
25 Participants108 Participants24 Participants25 Participants34 Participants
Race/Ethnicity, Customized
Other
8 Participants27 Participants9 Participants6 Participants4 Participants
Race/Ethnicity, Customized
White
91 Participants365 Participants91 Participants95 Participants88 Participants
Sex: Female, Male
Female
64 Participants281 Participants66 Participants83 Participants68 Participants
Sex: Female, Male
Male
60 Participants219 Participants58 Participants43 Participants58 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —— / —
other
Total, other adverse events
12 / 12418 / 12621 / 12617 / 124
serious
Total, serious adverse events
3 / 1248 / 1262 / 1260 / 124

Outcome results

Primary

Percentage Reduction in C-reactive Protein (CRP)

Time frame: 14 weeks

Population: As hsCRP was measured at both 6 and 14 weeks, linear mixed models conditioning on baseline hsCRP and adjusting for treatment stratum were constructed with the dependent variable being change in lnCRP. Any subject having either or both 6 week and 14 week measures was included.

ArmMeasureValue (MEAN)
Placebo PillPercentage Reduction in C-reactive Protein (CRP)-19.0 Percent CRP Reduction
Metformin PillPercentage Reduction in C-reactive Protein (CRP)-16.1 Percent CRP Reduction
Insulin Glargine Plus Placebo PillPercentage Reduction in C-reactive Protein (CRP)-2.9 Percent CRP Reduction
Insulin Glargine Plus Metformin PillPercentage Reduction in C-reactive Protein (CRP)-20.1 Percent CRP Reduction
Comparison: As hsCRP was measured at both 6 and 14 weeks, linear mixed models conditioning on baseline hsCRP and adjusting for treatment stratum were constructed with the dependent variable being change in lnCRP. The means at each time point were estimated from a repeated-measures model incorporating all 3 time points. The interventions were assessed by fitting terms corresponding to study drug and treatment arm assignment.p-value: <0.05Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026