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Combined Liraglutide and Metformin Therapy in Women With Previous Gestational Diabetes Mellitus (GDM)

Effects of Intervention With the Glucagon-like Peptide 1 (GLP-1) Analog Liraglutide Plus Metformin Versus Metformin Monotherapy in Overweight/Obese Women With Metabolic Defects and Recent History of Gestational Diabetes Mellitus (GDM)

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01234649
Enrollment
153
Registered
2010-11-04
Start date
2011-08-11
Completion date
2019-06-14
Last updated
2019-07-26

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

Conditions

Disorder of Glucose Regulation, Gestational Diabetes Mellitus, Impaired Glucose Tolerance, Metabolic Syndrome, Type 2 Diabetes Mellitus

Keywords

gestational diabetes mellitus, type 2 diabetes mellitus, metabolic dysfunction, impaired fasting glucose, impaired glucose tolerance, incretin mimetic

Brief summary

A diagnosis of gestational diabetes mellitus (GDM)has significant implications for the future health of the mother. GDM is often the culmination of years of unrecognized and unmodified diabetes risk factors that lead to overt and occult clinical manifestations during pregnancy. Systematic reviews of older studies conclude that 35-60% women with gestational diabetes will develop type 2 diabetes (DM2) at rates much greater than control groups who did not have glucose intolerance during pregnancy. Liraglutide may potentially delay disease progression in GDM considering the beta -(ß-)cell function improvement in DM2 and ß-cell mass shown to increase in animal models. This study will examine if the addition of liraglutide to metformin therapy is more effective than metformin alone in improving insulin sensitivity and normalizing insulin secretion in at-risk overweight/obese women with prior GDM.

Detailed description

Gestational diabetes is often the culmination of years of unrecognized and unmodified diabetes risk factors that lead to overt and occult clinical manifestations during pregnancy. . Despite the high and increasing rate of type 2 diabetes in Louisiana, the medical community does not have reliable estimates of the number of woman living in southern Louisiana who develop diabetes subsequent to GDM. Systematic reviews of older studies conclude that 35-60% women with gestational diabetes will develop type 2 diabetes at rates much greater than control groups who did not have glucose intolerance during pregnancy. The higher rates were in studies of particular ethnic groups in the U.S. Recently, follow-up programs elsewhere also have identified increasing rates of type 2 diabetes by 5-10 years after GDM: 9-43% type 2 diabetes in Europe and 11-21% in Asia. The frequency of type 2 diabetes is influenced by BMI, weight gain after pregnancy, family history of diabetes, fasting and postchallenge glucose levels during and after pregnancy, postpartum insulin resistance and inadequate β-cell secretion, and the need for pharmacological treatment during pregnancy. However, the risk factors are unable to predict all cases of subsequent type 2 diabetes: the biggest risk factor is a GDM pregnancy. Presently, in the literature, there are described new, more efficient methods of diabetes prevention in groups with a high risk of this disorder, which involve both, lifestyle modification and pharmacological therapies. Lifestyle intervention was found to reduce the incidence of type 2 diabetes by 58% and metformin by 31% as compared with placebo. The use of rosiglitazone in subjects with prediabetes resulted in a 60% reduction of the diabetes incidence rate. Studies are needed for optimal postpartum and long-term health of women who have had GDM. Considerable recent evidence suggests that incretin-based therapies may be useful for the treatment of DM2 because continuous administration of glucagon-like peptide 1 (GLP-1) produces substantial improvements in glucose control and ß-cell function in subjects with type 2 diabetes. Infusion of GLP-1 improves first and second-phase insulin secretion suggesting that early GLP-1 therapy may preserve ß-cell function in subjects with IGT or mild DM2. Whereas native GLP-1 has a very short half-life, the GLP-1 analogue liraglutide has a prolonged action (t1/2=13 h) suitable for once-daily injection. Liraglutide may potentially delay disease progression in GDM considering the ß-cell function improvement in DM2 and ß-cell mass shown to increase in animal models. This study will examine if the addition of liraglutide to metformin therapy is more effective than metformin alone in improving metabolic parameters in at-risk overweight/obese women with prior GDM

Interventions

DRUGMetformin XR plus placebo

Metformin plus Placebo Metformin 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid -98 weeks (end study) Placebo-start 1 injection SC QD step up to a max dose as tolerated

DRUGMetformin XR plus liraglutide

Metformin XR-500 qd for 2 weeks, 500 mg bid 2 weeks; 500 mg am, 1000 mg pm- 2 weeks - 1000 bid final dose Liraglutide- start 0.6 mg SC QD step up to 1.2 mg to a max dose of 1.8 mg SC QD as tolerated during the 4-wk non-forced dose-escalation period ( maximum allowed dose of 1.8 mg SC QD)

Sponsors

Novo Nordisk A/S
CollaboratorINDUSTRY
Woman's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult female 18 years to 45 years of age who experienced GDM within 52 weeks of index pregnancy * Actual BMI \>25 kg/ m2 * Written consent for participation in the study * Patient completed lactation * Dysglycemia (impaired fasting glucose \[IFG}, impaired glucose tolerance \[IGT} or IFG/IGT) and/or ß-cell dysfunction postpartum requiring pharmacological intervention (except type 1 or 2 diabetes)

Exclusion criteria

Personal or family history of medullary thyroid carcinoma or in patients with Multiple Endocrine Neoplasia syndrome type 2 * History of pancreatitis * Significant cardiovascular, cerebrovascular, renal, or hepatobiliary diseases in the past (viral hepatitis, toxic hepatic damage, jaundice of unknown etiology) * Serum liver enzymes (AST and/or ALT levels) exceeding more than twice normal laboratory values * Uncontrolled hypertension (systolic blood pressure\>150 mm Hg and/or diastolic blood pressure \>90 mm Hg) * Fasting serum triglycerides ≥800 mg/dl at screening. Lipid-lowering medications must have been maintained at the same dose for 3 months prior to enrollment * Hematological profiles considered to be clinically significant * Cholestasis during the past pregnancy * Presence of contradictions for GLP-1 receptor agonist or metformin administration such as allergy or hypersensitivity * Current use of metformin, thiazolidinediones, dipeptidyl peptidase-4 inhibitors or GLP-1 receptor agonist medications. * Use of drugs known to exacerbate glucose tolerance. * Use of prescription or over-the-counter weight-loss drugs * Diabetes postpartum or history of diabetes or prior use of medications to treat diabetes except gestational diabetes * Creatinine clearance less than 60 ml/min * History or currently undergoing chemotherapy or radiotherapy for cancer * Pregnancy planned during the coming two years * Currently breastfeeding *

Design outcomes

Primary

MeasureTime frameDescription
Insulin Secretion-Sensitivity Index (IS-SI)84 weeks of treatmentIS-SI in liraglutide-metformin (LIRA-MET) therapy compared to metformin alone (PLacebo-MET)

Secondary

MeasureTime frameDescription
Fasting Blood Glucose (FBG)84 weeks of treatmentFasting glucose levels in LIRA-MET group compared with PL-MET group
Mean Glucose During OGTT (MBG)84 weeks of treatmentMBG derived from average glucose measured during OGTT in LIRA-MET group compared with PL-MET group
Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)84 weeks of treatmentHOMA-IR, a measure of insulin resistance derived from fasting values, in LIRA-MET group compared with PL-MET group
Matsuda Insulin Sensitivity Index Derived From OGTT84 weeks of treatmentOGTT- derived insulin sensitivity index in LIRA-MET group compared with PL-MET group
Insulinogenic Index (IGI) /HOMA-IR84 weeks of treatmentIGI/HOMA-IR, a measure of early insulin response corrected by fasting insulin resistance, in LIRA-MET group compared with PL-MET group
Absolute Body Weight84 weeks of treatmentBody weight in LIRA-MET group compared with PL-MET group
Change in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline)Change from baseline (time 0) to study end (84 weeks)Change in body weight from baseline to end o f study in LIRA-MET group compared with PL-MET group. The number was derived from final weight minus baseline and normalized to a percent.
Body Mass Index (BMI)84 weeks of treatmentBMI, a measure of total body adiposity, in LIRA-MET group compared with PL-MET group
Waist Circumference (WC)84 weeks of treatmentWaist size (measure of truncal adiposity) with LIRA-MET compared to PL-MET
Waist-to-Hip Ratio (WHR)84 weeks of treatmentWaist circumference divided by hip circumference (a measure of central adiposity) in LIRA-MET group compared with PL-MET group
Triglyceride (TRG) Levels84 weeks of treatmentTRG concentrations in LIRA-MET group compared with PL-MET group
Total Cholesterol (CHOL) Levels84 weeks of treatmentCHOL levels in LIRA-MET group compared with PL-MET group
High Density Lipoprotein Cholesterol (HDL-C) Levels84 weeks of treatmentHDL-C levels in LIRA-MET group compared with PL-MET group
Low Density Lipoprotein Cholesterol (LDL-C) Levels84 weeks of treatmentLDL-Cholesterol levels in LIRA-MET group compared with PL-MET group
Triglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C)84 weeks of treatmentTRG/HDL-Cholesterol levels in LIRA-MET group compared with PL-MET group
Systolic Blood Pressure84 weeks of treatmentSBP in LIRA-MET group compared with PL-MET group
Diastolic Blood Pressure84 weeks of treatmentDBP in LIRA-MET group compared with PL-MET group
Alanine Aminotransferase (ALT) Levels84 weeks of treatmentHepatic enzyme, ALT, associated with insulin resistance, in LIRA-MET group compared with PL-MET group
Aspartate Aminotransferase (AST)84 weeks of treatmentThe hepatic marker, AST, associated with insulin resistance in LIRA-MET group compared with PL-MET group
Alanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio84 weeks of treatmentALT/AST ratio, used to assess liver function in LIRA-MET group compared with PL-MET group
Waist to Height Ratio (WHtR)84 weeks of treatmentWaist circumference divided by height (measure of body fat distribution) in LIRA-MET group compared with PL-MET group

Countries

United States

Participant flow

Recruitment details

153 met criteria and were randomized

Pre-assignment details

166 were consented but 153 met criteria

Participants by arm

ArmCount
Metformin XR Plus Liraglutide
Metformin XR plus Liraglutide Metformin extended release (XR) 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid- 84 weeks (end study) Liraglutide - start .6 mg SC QD step up to 1.2 mg to a max dose of 1.8 mg SC QD as tolerated Metformin XR plus liraglutide: Metformin XR-500 qd for 2 weeks, 500 mg bid 2 weeks; 500 mg am, 1000 mg pm- 2 weeks - 1000 bid final dose Liraglutide- start 0.6 mg SC QD step up to 1.2 mg to a max dose of 1.8 mg SC QD as tolerated during the 4-wk non-forced dose-escalation period ( maximum allowed dose of 1.8 mg SC QD)
78
Metformin XR Plus Placebo
Metformin plus Placebo Metformin 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid -84 weeks (end study) Placebo-start 1 injection SC QD step up to a max dose as tolerated Metformin XR plus placebo: Metformin plus Placebo Metformin 500 mg qd 2 weeks 500 mg bid 2 weeks 500 mg am, 1000 mg pm- 2 weeks 1000 mg bid -98 weeks (end study) Placebo-start 1 injection SC QD step up to a max dose as tolerated
75
Total153

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAllergic reaction10
Overall Studyintolerant to side effects43
Overall StudyLack of Efficacy03
Overall StudyPregnancy66
Overall StudyWithdrawal by Subject3226

Baseline characteristics

CharacteristicMetformin XR Plus LiraglutideMetformin XR Plus PlaceboTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
78 Participants75 Participants153 Participants
BMI greater than/equal to 2578 Participants75 Participants153 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
78 Participants75 Participants153 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
11 Participants17 Participants28 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
67 Participants58 Participants125 Participants
Region of Enrollment
United States
78 participants75 participants153 participants
Sex: Female, Male
Female
78 Participants75 Participants153 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 780 / 75
other
Total, other adverse events
30 / 7814 / 75
serious
Total, serious adverse events
0 / 780 / 75

Outcome results

Primary

Insulin Secretion-Sensitivity Index (IS-SI)

IS-SI in liraglutide-metformin (LIRA-MET) therapy compared to metformin alone (PLacebo-MET)

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideInsulin Secretion-Sensitivity Index (IS-SI)418.4 indexStandard Deviation 387
Metformin XR Plus PlaceboInsulin Secretion-Sensitivity Index (IS-SI)333 indexStandard Deviation 206
Comparison: Factorial repeated measures designp-value: <0.04ANOVA
Secondary

Absolute Body Weight

Body weight in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideAbsolute Body Weight94.2 kilogramsStandard Deviation 18.6
Metformin XR Plus PlaceboAbsolute Body Weight91.3 kilogramsStandard Deviation 20
Comparison: Factorial repeated measures ANOVAp-value: <0.048ANOVA
Secondary

Alanine Aminotransferase (ALT) Levels

Hepatic enzyme, ALT, associated with insulin resistance, in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideAlanine Aminotransferase (ALT) Levels32.3 U/LStandard Deviation 10.7
Metformin XR Plus PlaceboAlanine Aminotransferase (ALT) Levels31 U/LStandard Deviation 9.9
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Alanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio

ALT/AST ratio, used to assess liver function in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideAlanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio1.2 ratio of ALT (U/L)/ AST (U/L)Standard Deviation 0.4
Metformin XR Plus PlaceboAlanine Aminotransferase /Aspartate Aminotransferase (ALT/AST) Ratio1.18 ratio of ALT (U/L)/ AST (U/L)Standard Deviation 0.3
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Aspartate Aminotransferase (AST)

The hepatic marker, AST, associated with insulin resistance in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideAspartate Aminotransferase (AST)27 U/LStandard Deviation 8
Metformin XR Plus PlaceboAspartate Aminotransferase (AST)28 U/LStandard Deviation 10.5
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Body Mass Index (BMI)

BMI, a measure of total body adiposity, in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideBody Mass Index (BMI)33.8 weight (kg) /height (m) squaredStandard Deviation 5.2
Metformin XR Plus PlaceboBody Mass Index (BMI)32.8 weight (kg) /height (m) squaredStandard Deviation 6
Comparison: Factorial repeated measures ANOVAp-value: <0.047ANOVA
Secondary

Change in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline)

Change in body weight from baseline to end o f study in LIRA-MET group compared with PL-MET group. The number was derived from final weight minus baseline and normalized to a percent.

Time frame: Change from baseline (time 0) to study end (84 weeks)

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideChange in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline)-7.2 percent change in weight from baselineStandard Error 1.3
Metformin XR Plus PlaceboChange in Body Weight From Baseline to End of Study (Expressed as % Compared to Baseline)-3.1 percent change in weight from baselineStandard Error 1.4
p-value: <0.04ANOVA
Secondary

Diastolic Blood Pressure

DBP in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideDiastolic Blood Pressure77.6 mmHgStandard Deviation 8.9
Metformin XR Plus PlaceboDiastolic Blood Pressure77 mmHgStandard Deviation 9.9
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Fasting Blood Glucose (FBG)

Fasting glucose levels in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideFasting Blood Glucose (FBG)90 mg/dLStandard Deviation 6.4
Metformin XR Plus PlaceboFasting Blood Glucose (FBG)91.7 mg/dLStandard Deviation 8.4
Comparison: Factorial repeated measures ANOVAp-value: <0.005ANOVA
Secondary

High Density Lipoprotein Cholesterol (HDL-C) Levels

HDL-C levels in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideHigh Density Lipoprotein Cholesterol (HDL-C) Levels51 mg/dLStandard Deviation 12.6
Metformin XR Plus PlaceboHigh Density Lipoprotein Cholesterol (HDL-C) Levels48.7 mg/dLStandard Deviation 11.7
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)

HOMA-IR, a measure of insulin resistance derived from fasting values, in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideHomeostasis Model Assessment of Insulin Resistance (HOMA-IR)2.2 indexStandard Deviation 1.4
Metformin XR Plus PlaceboHomeostasis Model Assessment of Insulin Resistance (HOMA-IR)2.45 indexStandard Deviation 1.5
Comparison: Nested repeated measures designp-value: >0.05ANOVA
Secondary

Insulinogenic Index (IGI) /HOMA-IR

IGI/HOMA-IR, a measure of early insulin response corrected by fasting insulin resistance, in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideInsulinogenic Index (IGI) /HOMA-IR0.8 indexStandard Deviation 1.14
Metformin XR Plus PlaceboInsulinogenic Index (IGI) /HOMA-IR0.62 indexStandard Deviation 0.38
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Low Density Lipoprotein Cholesterol (LDL-C) Levels

LDL-Cholesterol levels in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideLow Density Lipoprotein Cholesterol (LDL-C) Levels110 mg/dLStandard Deviation 32
Metformin XR Plus PlaceboLow Density Lipoprotein Cholesterol (LDL-C) Levels107 mg/dLStandard Deviation 25
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Matsuda Insulin Sensitivity Index Derived From OGTT

OGTT- derived insulin sensitivity index in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideMatsuda Insulin Sensitivity Index Derived From OGTT5.9 indexStandard Deviation 2.9
Metformin XR Plus PlaceboMatsuda Insulin Sensitivity Index Derived From OGTT5.4 indexStandard Deviation 3.2
Comparison: Factorial repeated measures ANOVAp-value: <0.03ANOVA
Secondary

Mean Glucose During OGTT (MBG)

MBG derived from average glucose measured during OGTT in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideMean Glucose During OGTT (MBG)121.6 mg/dLStandard Deviation 20.8
Metformin XR Plus PlaceboMean Glucose During OGTT (MBG)118.8 mg/dLStandard Deviation 18.9
Comparison: Factorial repeated measures ANOVAp-value: <0.011ANOVA
Secondary

Systolic Blood Pressure

SBP in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideSystolic Blood Pressure122 mmHgStandard Deviation 12
Metformin XR Plus PlaceboSystolic Blood Pressure123 mmHgStandard Deviation 12
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Total Cholesterol (CHOL) Levels

CHOL levels in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideTotal Cholesterol (CHOL) Levels183.7 mg/dLStandard Deviation 36
Metformin XR Plus PlaceboTotal Cholesterol (CHOL) Levels183.8 mg/dLStandard Deviation 27
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA
Secondary

Triglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C)

TRG/HDL-Cholesterol levels in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideTriglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C)2.56 ratio of TRG (mg/dL)/HDL-C (mg/dl)Standard Deviation 1.5
Metformin XR Plus PlaceboTriglyceride to High Density Lipoprotein Cholesterol Ratio TRG/HDL-C)2.95 ratio of TRG (mg/dL)/HDL-C (mg/dl)Standard Deviation 2.9
Comparison: Factorial repeated measures ANOVAp-value: <0.049ANOVA
Secondary

Triglyceride (TRG) Levels

TRG concentrations in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideTriglyceride (TRG) Levels120 mg/dLStandard Deviation 64.5
Metformin XR Plus PlaceboTriglyceride (TRG) Levels125 mg/dLStandard Deviation 76.4
Comparison: Factorial repeated measures ANOVAp-value: <0.046ANOVA
Secondary

Waist Circumference (WC)

Waist size (measure of truncal adiposity) with LIRA-MET compared to PL-MET

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideWaist Circumference (WC)94.3 centimetersStandard Deviation 15.2
Metformin XR Plus PlaceboWaist Circumference (WC)95.3 centimetersStandard Deviation 15.2
Comparison: Factorial repeated measures ANOVAp-value: <0.023ANOVA
Secondary

Waist to Height Ratio (WHtR)

Waist circumference divided by height (measure of body fat distribution) in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideWaist to Height Ratio (WHtR).56 ratio of waist /heightStandard Deviation 0.08
Metformin XR Plus PlaceboWaist to Height Ratio (WHtR).57 ratio of waist /heightStandard Deviation 0.07
Comparison: Factorial repeated measures ANOVAp-value: 0.042ANOVA
Secondary

Waist-to-Hip Ratio (WHR)

Waist circumference divided by hip circumference (a measure of central adiposity) in LIRA-MET group compared with PL-MET group

Time frame: 84 weeks of treatment

ArmMeasureValue (MEAN)Dispersion
Metformin XR Plus LiraglutideWaist-to-Hip Ratio (WHR).81 ratio of waist/hip circumferenceStandard Deviation 0.04
Metformin XR Plus PlaceboWaist-to-Hip Ratio (WHR).81 ratio of waist/hip circumferenceStandard Deviation 0.05
Comparison: Factorial repeated measures ANOVAp-value: >0.05ANOVA

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026