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Efficacy, Safety, and Tolerability Study of Sotagliflozin as Adjunct Therapy in Adult Patients With Type 1 Diabetes Mellitus Who Have Inadequate Glycemic Control With Insulin Therapy

A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of LX4211 as Adjunct Therapy in Adult Patients With Type 1 Diabetes Mellitus Who Have Inadequate Glycemic Control With Insulin Therapy

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02421510
Acronym
inTandem2
Enrollment
782
Registered
2015-04-20
Start date
2015-05-31
Completion date
2017-06-23
Last updated
2020-02-12

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

Conditions

Type 1 Diabetes Mellitus

Keywords

High level of sugar (glucose) in the blood

Brief summary

This Phase 3 study was intended to demonstrate superiority of either Sotagliflozin high dose or low dose versus placebo on glycosylated hemoglobin A1C (A1C) reduction at Week 24 when used as an adjunct in adult participants with type 1 diabetes mellitus (T1D) who have inadequate glycemic control with insulin therapy.

Interventions

DRUGSotagliflozin

High dose Sotagliflozin, once daily, before the first meal of the day

DRUGPlacebo

Placebo, once daily, before the first meal of the day

Sponsors

Sanofi
CollaboratorINDUSTRY
Lexicon Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Participant who gave written informed consent to participate in the study in accordance with local regulations. * Adult participants 18 years and older with a diagnosis of T1D made at least 1 year prior to informed consent. * Participants treated with insulin or insulin analog delivered via continuous subcutaneous insulin infusion (CSII) or multiple daily injections (MDI). * Willing and were able to perform Self-monitoring of blood glucose (SMBG) and completed the study diary as required per protocol. * At the Screening Visit, A1C was between 7.0% to 11.0%. * Females of childbearing potential must use an adequate method of contraception and have a negative pregnancy test.

Exclusion criteria

* Use of antidiabetic agent other than insulin or insulin analog at the time of screening. * Use of sodium-glucose cotransporter (SGLT) inhibitors within 8 weeks prior to screening. * Chronic systemic corticosteroid use. * Type 2 diabetes mellitus (T2DM), or severely uncontrolled T1D as determined by the Investigator.

Design outcomes

Primary

MeasureTime frameDescription
Change From Baseline in A1C at Week 24Baseline to Week 24Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. Least square (LS) means were obtained from a mixed-effects model for repeated measures (MMRM) that included fixed, categorical effects of treatment, randomization strata of insulin delivery method (MDI, CSII), randomization strata of Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), a treatment-by-time interaction, and baseline A1C-by-time interaction as a covariate. A negative change from baseline (a reduction of A1C value at Week 24) indicates an improvement.

Secondary

MeasureTime frameDescription
Change From Baseline in Body Weight at Week 24Baseline to Week 24Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model. A negative change from baseline indicates a loss in body weight from baseline to Week 24.
Change From Baseline in Mean Daily Bolus Insulin Dose at Week 24Baseline to Week 24The mean bolus insulin dose in international units/day (IU/day) for Week 24 was the average over the 3 to 5 days prior to the Week 24 visit. The Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model including all available post baseline values. A negative change from baseline indicated a reduction in the amount of bolus insulin used and a positive change from baseline indicated an increase in the amount of bolus insulin used between baseline and Week 24.
Change From Baseline in Fasting Plasma Glucose (FPG) at Week 24Baseline to Week 24The Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model including all available post baseline values. A negative change from baseline indicates a lower glucose level at Week 24 compared to baseline and a positive change from baseline indicates an increase in glucose level at Week 24 compared to baseline.
Percentage of Participants With A1C <7.0% at Week 24 and no Episode of Severe Hypoglycemia, and no Episode of Diabetic Ketoacidosis (DKA) From Baseline to Week 24Baseline to Week 24The composite endpoint included blood samples for the assessment of Hemoglobin A1C to determine the participants with a value \<7.0% and a central blinded adjudication process to determine whether participants experienced either DKA or severe hypoglycemia. Only positively adjudicated severe hypoglycemia and diabetic ketoacidosis were included in the analysis.
Change From Baseline in 2-Item Diabetes Distress Screen 2 (DDS2) Score at Week 24Baseline to Week 24DDS2 is a 2-item diabetes distress screening instrument where participants rated the degree to which the following items caused distress: (1) feeling overwhelmed by the demands of living with diabetes, and (2) feeling that I am often failing with my diabetes regimen using a 6-point scale: where 1=no distress to 6=severe distress for a total possible score of 2 to 12. LS means were obtained from MMRM model including all available post baseline values. A negative change from baseline indicates improvement.
Percent Change From Baseline in Body Weight at Week 24Baseline to Week 24Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model. A negative percent change from baseline indicates a loss in body weight from baseline to Week 24.
Change From Baseline in Diabetes Treatment Satisfaction Questionnaire (DTSQ) Score at Week 24Baseline to Week 24The DTSQ instrument contains 8 items assessing overall treatment satisfaction, treatment convenience and flexibility, satisfaction with understanding of diabetes, willingness to continue present treatment and to recommend it to others, and frequency of unacceptably high and unacceptably low blood glucose levels. 6 items (1, 4, 5, 6, 7 and 8) (excluding perceived hyperglycemia and hypoglycemia items) were scored using a 7- point scale where 0=very dissatisfied to 6= very satisfied for a total possible score of 0 (very dissatisfied) to 36 (very satisfied), where higher scores indicate higher satisfaction from treatment. Two items (Q2 and 3), which were not included, measured perceived hyperglycemia and hypoglycemia, respectively. The baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model including all available post baseline values. A positive change from baseline indicates improvement.

Countries

Austria, Belgium, Bulgaria, France, Germany, Hungary, Israel, Italy, Lithuania, Netherlands, Poland, Romania, Slovakia, Spain, Sweden, Switzerland, United Kingdom

Participant flow

Recruitment details

Participants took part in the study at 96 investigative sites throughout 17 countries from 21 May 2015 to 23 June 2017.

Pre-assignment details

995 participants were screened and 782 participants with a diagnosis of Type 1 diabetes mellitus were randomized equally in 1 of 3 treatment groups: sotagliflozin 400 mg, sotagliflozin 200 mg or placebo.

Participants by arm

ArmCount
Placebo
Two placebo-matching sotagliflozin tablets, once daily, orally, before the first meal of the day for 24 weeks followed by a 28-week extension period.
258
Sotagliflozin 200 mg
Sotagliflozin 200 mg (one 200 mg tablet and one placebo tablet), once daily, orally, before the first meal of the day for 24 weeks followed by a 28-week extension period.
261
Sotagliflozin 400 mg
Sotagliflozin 400 mg (two 200 mg tablets), once daily, orally, before the first meal of the day for 24 weeks followed by a 28-week extension period.
263
Total782

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyAdverse Event91018
Overall StudyDeath100
Overall StudyLost to Follow-up110
Overall StudyNoncompliance with study drug100
Overall StudyOther423
Overall StudyPhysician Decision113
Overall StudyPregnancy110
Overall StudyProtocol Violation120
Overall StudyWithdrawal by Subject141812

Baseline characteristics

CharacteristicPlaceboSotagliflozin 200 mgSotagliflozin 400 mgTotal
Age, Continuous39.7 Years
STANDARD_DEVIATION 13.42
42.3 Years
STANDARD_DEVIATION 13.59
41.7 Years
STANDARD_DEVIATION 13.23
41.2 Years
STANDARD_DEVIATION 13.44
Age, Customized
Adults (18-64 years)
244 Participants252 Participants253 Participants749 Participants
Age, Customized
From 65-84 years
14 Participants9 Participants10 Participants33 Participants
Body Weight81.08 Kilograms (kg)
STANDARD_DEVIATION 16.857
81.93 Kilograms (kg)
STANDARD_DEVIATION 17.386
81.97 Kilograms (kg)
STANDARD_DEVIATION 17.963
81.66 Kilograms (kg)
STANDARD_DEVIATION 17.394
Daily Total Insulin Dose0.75 International units per kilogram (IU/kg)
STANDARD_DEVIATION 0.295
0.73 International units per kilogram (IU/kg)
STANDARD_DEVIATION 0.277
0.74 International units per kilogram (IU/kg)
STANDARD_DEVIATION 0.267
0.74 International units per kilogram (IU/kg)
STANDARD_DEVIATION 0.28
Duration of Diabetes18.1 Years
STANDARD_DEVIATION 10.72
18.2 Years
STANDARD_DEVIATION 10.82
18.9 Years
STANDARD_DEVIATION 11.18
18.4 Years
STANDARD_DEVIATION 10.9
Hemoglobin A1C (A1C)
<= 8.5%
200 Participants203 Participants204 Participants607 Participants
Hemoglobin A1C (A1C)
>8.5%
58 Participants58 Participants59 Participants175 Participants
Hemoglobin A1C Value at Actual Week -2 Value
<= 8.5%
202 Participants205 Participants208 Participants615 Participants
Hemoglobin A1C Value at Actual Week -2 Value
>8.5%
56 Participants56 Participants55 Participants167 Participants
Insulin Delivery Method
Continuous Subcutaneous Insulin Infusion (CSII)
66 Participants68 Participants67 Participants201 Participants
Insulin Delivery Method
Multiple Daily Injections (MDI)
192 Participants193 Participants196 Participants581 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants3 Participants3 Participants6 Participants
Race (NIH/OMB)
Black or African American
1 Participants0 Participants0 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
7 Participants6 Participants10 Participants23 Participants
Race (NIH/OMB)
White
250 Participants252 Participants250 Participants752 Participants
Sex: Female, Male
Female
124 Participants122 Participants130 Participants376 Participants
Sex: Female, Male
Male
134 Participants139 Participants133 Participants406 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
2 / 2580 / 2610 / 263
other
Total, other adverse events
46 / 25852 / 26164 / 263
serious
Total, serious adverse events
17 / 25826 / 26121 / 263

Outcome results

Primary

Change From Baseline in A1C at Week 24

Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. Least square (LS) means were obtained from a mixed-effects model for repeated measures (MMRM) that included fixed, categorical effects of treatment, randomization strata of insulin delivery method (MDI, CSII), randomization strata of Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), a treatment-by-time interaction, and baseline A1C-by-time interaction as a covariate. A negative change from baseline (a reduction of A1C value at Week 24) indicates an improvement.

Time frame: Baseline to Week 24

Population: Analysis included participants from the modified intent to treat (mITT) population. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange From Baseline in A1C at Week 24-0.02 Percentage of A1CStandard Error 0.044
Sotagliflozin 200 mgChange From Baseline in A1C at Week 24-0.39 Percentage of A1CStandard Error 0.044
Sotagliflozin 400 mgChange From Baseline in A1C at Week 24-0.37 Percentage of A1CStandard Error 0.043
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline A1C-by-time interaction as a covariate.p-value: <0.00195% CI: [-0.48, -0.25]MMRM
Comparison: LS means and p-values were obtained from Mixed effect Model Repeat Measurement (MMRM) model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline A1C- by-time interaction as a covariate.p-value: <0.00195% CI: [-0.47, -0.24]MMRM
Secondary

Change From Baseline in 2-Item Diabetes Distress Screen 2 (DDS2) Score at Week 24

DDS2 is a 2-item diabetes distress screening instrument where participants rated the degree to which the following items caused distress: (1) feeling overwhelmed by the demands of living with diabetes, and (2) feeling that I am often failing with my diabetes regimen using a 6-point scale: where 1=no distress to 6=severe distress for a total possible score of 2 to 12. LS means were obtained from MMRM model including all available post baseline values. A negative change from baseline indicates improvement.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange From Baseline in 2-Item Diabetes Distress Screen 2 (DDS2) Score at Week 240.0 Score on a scaleStandard Error 0.12
Sotagliflozin 200 mgChange From Baseline in 2-Item Diabetes Distress Screen 2 (DDS2) Score at Week 24-0.3 Score on a scaleStandard Error 0.12
Sotagliflozin 400 mgChange From Baseline in 2-Item Diabetes Distress Screen 2 (DDS2) Score at Week 24-0.4 Score on a scaleStandard Error 0.11
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline DDS2 total score-by-time interaction as a covariate.p-value: 0.02595% CI: [-0.6, 0]MMRM
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<=8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline DDS2 total score-by-time interaction as a covariate.p-value: 0.00395% CI: [-0.7, -0.2]MMRM
Secondary

Change From Baseline in Body Weight at Week 24

Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model. A negative change from baseline indicates a loss in body weight from baseline to Week 24.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange From Baseline in Body Weight at Week 240.11 Kilograms (kg)Standard Error 0.201
Sotagliflozin 200 mgChange From Baseline in Body Weight at Week 24-1.88 Kilograms (kg)Standard Error 0.2
Sotagliflozin 400 mgChange From Baseline in Body Weight at Week 24-2.47 Kilograms (kg)Standard Error 0.199
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects.p-value: <0.00195% CI: [-2.53, -1.44]MMRM
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects.p-value: <0.00195% CI: [-3.12, -2.04]MMRM
Secondary

Change From Baseline in Diabetes Treatment Satisfaction Questionnaire (DTSQ) Score at Week 24

The DTSQ instrument contains 8 items assessing overall treatment satisfaction, treatment convenience and flexibility, satisfaction with understanding of diabetes, willingness to continue present treatment and to recommend it to others, and frequency of unacceptably high and unacceptably low blood glucose levels. 6 items (1, 4, 5, 6, 7 and 8) (excluding perceived hyperglycemia and hypoglycemia items) were scored using a 7- point scale where 0=very dissatisfied to 6= very satisfied for a total possible score of 0 (very dissatisfied) to 36 (very satisfied), where higher scores indicate higher satisfaction from treatment. Two items (Q2 and 3), which were not included, measured perceived hyperglycemia and hypoglycemia, respectively. The baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model including all available post baseline values. A positive change from baseline indicates improvement.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange From Baseline in Diabetes Treatment Satisfaction Questionnaire (DTSQ) Score at Week 24-0.1 Score on a scaleStandard Error 0.28
Sotagliflozin 200 mgChange From Baseline in Diabetes Treatment Satisfaction Questionnaire (DTSQ) Score at Week 241.9 Score on a scaleStandard Error 0.28
Sotagliflozin 400 mgChange From Baseline in Diabetes Treatment Satisfaction Questionnaire (DTSQ) Score at Week 241.6 Score on a scaleStandard Error 0.28
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline DTSQs total score-by-time interaction as a covariate.p-value: <0.00195% CI: [1.3, 2.7]MMRM
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline DTSQs total score-by-time interaction as a covariate.p-value: <0.00195% CI: [1, 2.4]MMRM
Secondary

Change From Baseline in Fasting Plasma Glucose (FPG) at Week 24

The Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model including all available post baseline values. A negative change from baseline indicates a lower glucose level at Week 24 compared to baseline and a positive change from baseline indicates an increase in glucose level at Week 24 compared to baseline.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange From Baseline in Fasting Plasma Glucose (FPG) at Week 248.8 Milligram per deciliter (mg/dL)Standard Error 3.95
Sotagliflozin 200 mgChange From Baseline in Fasting Plasma Glucose (FPG) at Week 24-12.8 Milligram per deciliter (mg/dL)Standard Error 3.97
Sotagliflozin 400 mgChange From Baseline in Fasting Plasma Glucose (FPG) at Week 24-16.9 Milligram per deciliter (mg/dL)Standard Error 3.96
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline Fasting Plasma Glucose-by-time interaction as a covariate.p-value: <0.00195% CI: [-32.2, -11]MMRM
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and baseline Fasting Plasma Glucose-by-time interaction as a covariate.p-value: <0.00195% CI: [-36.2, -15.1]MMRM
Secondary

Change From Baseline in Mean Daily Bolus Insulin Dose at Week 24

The mean bolus insulin dose in international units/day (IU/day) for Week 24 was the average over the 3 to 5 days prior to the Week 24 visit. The Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model including all available post baseline values. A negative change from baseline indicated a reduction in the amount of bolus insulin used and a positive change from baseline indicated an increase in the amount of bolus insulin used between baseline and Week 24.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange From Baseline in Mean Daily Bolus Insulin Dose at Week 24-1.19 IU/dayStandard Error 0.635
Sotagliflozin 200 mgChange From Baseline in Mean Daily Bolus Insulin Dose at Week 24-4.38 IU/dayStandard Error 0.636
Sotagliflozin 400 mgChange From Baseline in Mean Daily Bolus Insulin Dose at Week 24-4.78 IU/dayStandard Error 0.634
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and Baseline mean daily bolus insulin dose-by-time interaction as a covariate.p-value: <0.00195% CI: [-4.86, -1.53]MMRM
Comparison: LS means and p-values were obtained from MMRM model with treatment, randomization strata of insulin delivery (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%), time (study week), and a treatment-by-time interaction as fixed categorical effects, and Baseline mean daily bolus insulin dose-by-time interaction as a covariate.p-value: <0.00195% CI: [-5.25, -1.93]MMRM
Secondary

Percentage of Participants With A1C <7.0% at Week 24 and no Episode of Severe Hypoglycemia, and no Episode of Diabetic Ketoacidosis (DKA) From Baseline to Week 24

The composite endpoint included blood samples for the assessment of Hemoglobin A1C to determine the participants with a value \<7.0% and a central blinded adjudication process to determine whether participants experienced either DKA or severe hypoglycemia. Only positively adjudicated severe hypoglycemia and diabetic ketoacidosis were included in the analysis.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population.

ArmMeasureValue (NUMBER)
PlaceboPercentage of Participants With A1C <7.0% at Week 24 and no Episode of Severe Hypoglycemia, and no Episode of Diabetic Ketoacidosis (DKA) From Baseline to Week 2415.1 Percentage of participants
Sotagliflozin 200 mgPercentage of Participants With A1C <7.0% at Week 24 and no Episode of Severe Hypoglycemia, and no Episode of Diabetic Ketoacidosis (DKA) From Baseline to Week 2431.4 Percentage of participants
Sotagliflozin 400 mgPercentage of Participants With A1C <7.0% at Week 24 and no Episode of Severe Hypoglycemia, and no Episode of Diabetic Ketoacidosis (DKA) From Baseline to Week 2432.3 Percentage of participants
Comparison: P-values were obtained from a Cochran-Mantel-Haenszel (CMH) test stratified by the different levels of the randomization stratification factors of insulin delivery method (MDI, CSII) and Week -2 A1C (\<=8.5%, \>8.5%). The 95% Confidence Limits (CL) were calculated using asymptotic Wald method. Only positively adjudicated severe hypoglycemia and diabetic ketoacidosis were included in the analysis.p-value: <0.00195% CI: [9.17, 23.43]Cochran-Mantel-Haenszel
Comparison: P-values were obtained from a CMH test stratified by the different levels of the randomization stratification factors of insulin delivery method (MDI, CSII) and Week -2 A1C (\<= 8.5%, \>8.5%). The 95% CL were calculated using asymptotic Wald method.p-value: <0.00195% CI: [10.06, 24.35]Cochran-Mantel-Haenszel
Secondary

Percent Change From Baseline in Body Weight at Week 24

Baseline value was defined as the last value collected prior to the first dose of double-blind study medication. LS means were obtained from MMRM model. A negative percent change from baseline indicates a loss in body weight from baseline to Week 24.

Time frame: Baseline to Week 24

Population: Analysis included participants from the mITT population, including all available post baseline values. Here, overall number of participants analyzed = participants with available data for this outcome measure.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboPercent Change From Baseline in Body Weight at Week 240.10 Percent changeStandard Error 0.245
Sotagliflozin 200 mgPercent Change From Baseline in Body Weight at Week 24-2.38 Percent changeStandard Error 0.245
Sotagliflozin 400 mgPercent Change From Baseline in Body Weight at Week 24-2.99 Percent changeStandard Error 0.244

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026