Type I Diabetes Mellitus
Conditions
Keywords
Combined treatment of patients with type I diabetes mellitus
Brief summary
The purpose of this study is: * to assess clinical efficacy of Subetta in the combined treatment of type I diabetes mellitus; * to assess safety of Subetta in the combined treatment of type I diabetes mellitus.
Detailed description
Patients with type I diabetes mellitus are included in the trial. It is concerned those patients, who by the time of the trial receive basal bolus insulin therapy of type I diabetes mellitus, including basal insulin (using long acting medications) and prandial insulin (short and ultra short acting medications), and with poor glycemic control (HbA1c=7.0-10.0%). For patients, which will be included in the trial (mainly middle aged patients without severe complications of diabetes), HbA1c\>7.0% is the marker showing that optimal individual goal of glycemic control is not achieved. HbA1c, fasting plasma glucose, microalbuminuria, estimated glomerular filtration rate, ophthalmoscopy, blood pressure measurement, patient self-monitoring of blood glucose, frequency of hypoglycemia, endocrinologist examination were performed within screening period. Patients without severe diabetes complications are randomized in 2 groups. If a patient meets inclusion criteria and does not show exclusion criteria he/she is randomized in one of 2 groups: Group 1 - patients receiving standard type I diabetes mellitus therapy + Subetta at a dose of 1 tablet 4 times a day; Group 2 - the group receiving standard type I diabetes mellitus therapy + Placebo under the regimen used for Subetta. The invented names of the drugs containing basal and prandial (meal) insulin should be unchanged for each patient during the whole trial. All patients will receive glucometers and the appropriate glucose test strips, so they could self monitor blood glucose and register this data in their diaries. The trial duration is 38 weeks; the main stages of the trial are conducted during screening, then in 4 weeks (Visit 2), in 12 weeks (Visit 3), in 24 weeks (Visit 4) and in 36 weeks (Visit 5). In 1 week after randomization and the onset of the trial therapy and between the visits to the study site (on weeks 8±1, 18±1 and 30±1) an investigator collects data on patient's health and complaints (phone visits) to decide whether it is necessary to arrange unplanned visit to the site.
Interventions
DRUGSubetta
Each Subetta tablet contains a mixture of affinity purified polyclonal antibodies to β-subunit of the rINS (6 mg) and antibodies to eNOS (6 mg) in released-active form produced by the patented technology in accordance with the applicable European Pharmacopeia requirements. Standard therapy of type I diabetes mellitus + Subetta (1 tablet 4 times a day) for 36 weeks. Subetta: oral administration, per 1 intake - 1 tablet (keep in the mouth until complete dissolution, not at mealtime).
DRUGPlacebo
Placebo (identical to Subetta in shape and taste tablet containing exсipients). Standard therapy of type I diabetes mellitus + Placebo (1 tablet 4 times a day) for 36 weeks. Placebo: oral administration, per 1 intake - 1 tablet (keep in the mouth until complete dissolution, not at mealtime).
Sponsors
Materia Medica Holding
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Diagnosed type I diabetes mellitus (according to WHO criteria, 1999 - 2006). 2. Disease duration no less than 6 months. 3. Patient's age from 18 to 65 years inclusive. 4. Level of glycosylated hemoglobin 7.0- 10.0 %. 5. Glomerular filtration rate ≥ 60 ml/ min/1.73m\^2. 6. Stable dose of basal insulin for the last 3 months. (Permissible fluctuations are ±10%.) 7. Usage of contraceptive methods by both gender patients of reproductive age during the trial and within 30 days after ending the participation in the trial. 8. Availability of signed patient information sheet (Informed Consent form) for participation in the clinical trial.
Exclusion criteria
1. Acute diabetes mellitus complications for 3 months prior to inclusion in the trial (diabetic ketoacidosis, hyperosmolar hyperglycemic state, lacticemia, severe hypoglycemia and hypoglycemic coma). 2. Diabetic retinopathy, preproliferative, proliferative or terminal stages (based on the results of oculist examination during screening period or 6 months prior to the trial). 3. Diabetic nephropathy, proteinuria stage, chronic kidney disease on 3, 4 or 5 stage. 4. Diabetic microangiopathy: * ishemic heart disease (medical history of a sudden coronary death with successful reanimation, medical history of myocardial infarction, stable exertional angina III or IV FC; unstable angina; post-infarction cardiosclerosis; chronic heart failure III or IV FC); * cerebrovascular diseases (medical history of acute cerebrovascular accident; progressive vascular leukoencephalopathy; vascular dementia); * chronic obliterative peripheral vascular diseases (clinically significant); * diabetic neuroosteoarthropathy; * diabetic foot (clinically significant). 5. Heart rhythm disorder: * II-III atrioventricular block; * sick sinus syndrome; * long QT interval syndrome; * complete left bundle branch block; * block of 2/3 bundle branches; * WPW syndrome; * ventricular arrhythmia of III grade according Laun-Wolf; * paroxysmal supraventricular tachycardia; * paroxysmal/recurrent ventricular tachycardia; * atrial flutter and fibrillation; * ventricular flutter and fibrillation; * heart pacemaker implant. 6. Uncontrolled arterial hypertension characterized by the following blood tension values: systolic blood pressure over 160 mm Hg and/or diastolic blood pressure over 100 mm Hg. 7. Severe concomitant pathology including clinically significant cardiovascular diseases of III - IV functional class (according to New York Heart Association classification, 1964), nervous and endocrine system diseases, including morbid obesity (body mass index≥40.0 kg/m2), renal insufficiency, liver failure. 8. Medical history of pancreatectomy or transplantation of pancreatic/islet cells. 9. Medical history of renal transplantation. 10. Malignant neoplasms/suspected malignant neoplasms. 11. Exacerbations or decompensation of chronic diseases affecting a patient's ability to participate in the clinical trial. 12. Level of fasting triglycerides \>5.64 mmol/L. 13. Medical history of bariatric surgical operations. 14. Medical history of polyvalent allergy. 15. Allergy/ intolerance to any of the components of medications used in the treatment. 16. Intake of medicines listed in the section Prohibited concomitant treatment for 3 months prior to the inclusion in the trial. 17. Pregnancy, breast-feeding. 18. Drug addiction, alcohol usage in the amount exceeding 2 units of alcohol per day. 19. Mental disorders of a patient. 20. Night work. 21. Participation in other clinical trials in the course of 3 months prior to the inclusion in the trial. 22. Patients, who from the investigator's point of view, will fail to comply with the observation requirements of the trial or with the intake regimen of the investigated medicines. 23. Other factors impeding patient's participation in the trial (for example, planned business trips or journeys). 24. Patient is related to the research personnel of the investigative site, who are directly involved in the trial or are the immediate relative of the researcher. The immediate relative includes husband/wife, parents, children or brothers (or sisters), regardless of whether they are natural or adopted. 25. Patient works for OOO NPF Materia Medica Holding (i.e. is the company's employee, temporary contract worker or appointed official responsible for the carrying out the research) or the immediate relative.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the Mean Value of HbA1c | baseline and 12, 24 and 36 weeks of the treatment | The HbA1C test was performed using a method that is certified by the National Glycohemoglobin Standardization Program (NGSP) (www.ngsp.org) and standardized or traceable to the Diabetes Control and Complications Trial (DCCT) reference assay. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | baseline and 4, 8, 12, 18, 24, 30 and 36 weeks of the treatment | A 7-point patient self-monitoring of blood glucose (SMBG): three measurements of blood glucose before the meal; three measurements of postprandial blood glucose (1-2 h after the start of the meal) and one measurement at 3:00 a.m. |
| Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | baseline and 12, 24 and 36 weeks of the treatment | Blood samples (for measurement of fasting plasma glucose, concentrations of plasma total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides) are taken under standard conditions: after night break in food taking (at least 12 hours) and prior to administering of insulin morning dose (prandial), prior to any morning medicines intake (including the study drug and permitted concomitant therapy). |
| Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | baseline and 4, 12, 24 and 36 weeks of the treatment | — |
| Changes in Dosage of Total Insulin Measured in IU/kg of Body Weight | baseline and 36 weeks of the treatment | Insulin dose should be corrected by a patient on a daily basis taking into consideration data on blood glucose self- monitoring during a day and amount of food carbohydrates. Physician can correct insulin dose based on the same data. |
| Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | 36 weeks of the treatment | The Diabetes Treatment Satisfaction Questionnaire allows to assess the degree of satisfaction with treatment for diabetes and its complications - retinopathy and nephropathy, how patients' satisfaction and perceived hyper- and hypoglycemia have changed compared to the initial period (before the treatment). The Diabetes Treatment Satisfaction Questionnaire contains six items scored on 7-point scales from +3 (equals very satisfied) to -3 (equals very dissatisfied), with 0 (equals no change). These are summed to produce a total Treatment Satisfaction score. Two questions concerning Perceived Hyperglycaemia and Perceived Hypoglycaemia respectively, are calculated separately. According to these two items, low scores represent good perceived blood glucose control (+3 means most of the time of Hyperglycaemia or Hypoglycaemia whereas -3 means none of the time of Hyperglycaemia or Hypoglycaemia). |
| Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | baseline and 36 weeks of the treatment | Insulin dose should be corrected by a patient on a daily basis taking into consideration data on blood glucose self- monitoring during a day and amount of food carbohydrates. Physician can correct insulin dose based on the same data. |
Countries
Russia
Participant flow
Recruitment details
The study enrolled patients using intensive insulin regimen (Short-acting and Long-acting human insulins) with type 1 diabetes who were not meeting glycemic control (HbA1c\>7.0%). Eligible patients were assessed by endocrinologists. The study was performed in 15 medical institutions in Russia from May 2013 to October 2015.
Pre-assignment details
Selection procedures were carried out after participant enrollment to determine whether the patient could participate in the study in accordance with the inclusion/exclusion criteria. Of the 200 patients enrolled, 49 did not meet inclusion criteria after screening procedures, they were not randomized
Participants by arm
| Arm | Count |
|---|---|
| Subetta Short-acting and Long-acting human insulins + Subetta (1 tablet 4 times a day). Subetta: oral administration, per 1 intake - 1 tablet (keep in the mouth until complete dissolution, not at mealtime).
Subetta: Efficacy and Safety of Subetta in the combined treatment of patients with type I diabetes mellitus | 72 |
| Placebo Short-acting and Long-acting human insulins + Placebo (1 tablet 4 times a day). Placebo: oral administration, per 1 intake - 1 tablet (keep in the mouth until complete dissolution, not at mealtime).
Placebo | 72 |
| Total | 144 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Do not meet inclusion criteria | 4 | 3 |
Baseline characteristics
| Characteristic | Subetta | Placebo | Total |
|---|---|---|---|
| Age, Continuous | 37.2 years STANDARD_DEVIATION 9.6 | 35.0 years STANDARD_DEVIATION 10.4 | 36.1 years STANDARD_DEVIATION 10 |
| Sex: Female, Male Female | 34 Participants | 36 Participants | 70 Participants |
| Sex: Female, Male Male | 38 Participants | 36 Participants | 74 Participants |
| Weight | 77.7 kilogram STANDARD_DEVIATION 15.2 | 74.4 kilogram STANDARD_DEVIATION 13.5 | 76.0 kilogram STANDARD_DEVIATION 14.4 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 16 / 76 | 18 / 75 |
| serious Total, serious adverse events | 2 / 76 | 3 / 75 |
Outcome results
Primary
Changes in the Mean Value of HbA1c
The HbA1C test was performed using a method that is certified by the National Glycohemoglobin Standardization Program (NGSP) (www.ngsp.org) and standardized or traceable to the Diabetes Control and Complications Trial (DCCT) reference assay.
Time frame: baseline and 12, 24 and 36 weeks of the treatment
Population: Intention-to-Treat set
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Subetta | Changes in the Mean Value of HbA1c | 12 weeks | -0.71 percentage of HbA1c | Standard Deviation 0.91 |
| Subetta | Changes in the Mean Value of HbA1c | 24 weeks | -0.66 percentage of HbA1c | Standard Deviation 0.94 |
| Subetta | Changes in the Mean Value of HbA1c | 36 weeks | -0.59 percentage of HbA1c | Standard Deviation 0.99 |
| Placebo | Changes in the Mean Value of HbA1c | 12 weeks | -0.49 percentage of HbA1c | Standard Deviation 1.02 |
| Placebo | Changes in the Mean Value of HbA1c | 24 weeks | -0.27 percentage of HbA1c | Standard Deviation 1.13 |
| Placebo | Changes in the Mean Value of HbA1c | 36 weeks | -0.20 percentage of HbA1c | Standard Deviation 1.14 |
p-value: 0.019Mixed Models Analysis
Secondary
Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG)
A 7-point patient self-monitoring of blood glucose (SMBG): three measurements of blood glucose before the meal; three measurements of postprandial blood glucose (1-2 h after the start of the meal) and one measurement at 3:00 a.m.
Time frame: baseline and 4, 8, 12, 18, 24, 30 and 36 weeks of the treatment
Population: Intention-to-Treat. 2 patients (1 in Subetta group and 1 in Placebo group) was excluded from the analysis due to lake of diaries
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 12 weeks | -0.2 mmol / l | Standard Deviation 1.6 |
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 24 weeks | -0.3 mmol / l | Standard Deviation 1.7 |
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 8 weeks | -0.2 mmol / l | Standard Deviation 1.7 |
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 30 weeks | 0.0 mmol / l | Standard Deviation 1.8 |
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 18 weeks | -0.1 mmol / l | Standard Deviation 2.2 |
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 36 weeks | -0.1 mmol / l | Standard Deviation 1.9 |
| Subetta | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 4 weeks | -0.1 mmol / l | Standard Deviation 1.4 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 36 weeks | 0.0 mmol / l | Standard Deviation 2 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 4 weeks | 0.1 mmol / l | Standard Deviation 1.8 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 8 weeks | -0.1 mmol / l | Standard Deviation 2 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 12 weeks | -0.2 mmol / l | Standard Deviation 2 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 18 weeks | -0.1 mmol / l | Standard Deviation 1.9 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 24 weeks | 0.0 mmol / l | Standard Deviation 2 |
| Placebo | Change in Average Daily Blood Glucose From a 7-point Patient Self-monitoring of Blood Glucose (SMBG) | 30 weeks | -0.1 mmol / l | Standard Deviation 1.8 |
p-value: 0.7344Mixed Models Analysis
Secondary
Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis)
Time frame: baseline and 4, 12, 24 and 36 weeks of the treatment
Population: Intention-to-Treat set
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Subetta | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 4 weeks | -0.5 mmol / l | Standard Deviation 5.1 |
| Subetta | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 12 weeks | -0.2 mmol / l | Standard Deviation 4.8 |
| Subetta | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 24 weeks | -0.7 mmol / l | Standard Deviation 4.9 |
| Subetta | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 36 weeks | -0.8 mmol / l | Standard Deviation 4.8 |
| Placebo | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 36 weeks | 1.1 mmol / l | Standard Deviation 5.4 |
| Placebo | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 4 weeks | 0.3 mmol / l | Standard Deviation 4.6 |
| Placebo | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 24 weeks | 0.7 mmol / l | Standard Deviation 5.4 |
| Placebo | Change in Fasting Plasma Glucose (Based on the Data of Biochemical Analysis) | 12 weeks | 0.8 mmol / l | Standard Deviation 4.9 |
p-value: 0.0432Mixed Models Analysis
Secondary
Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU)
Insulin dose should be corrected by a patient on a daily basis taking into consideration data on blood glucose self- monitoring during a day and amount of food carbohydrates. Physician can correct insulin dose based on the same data.
Time frame: baseline and 36 weeks of the treatment
Population: Intention-to-Treat set
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Subetta | Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | Basal insulin (36 weeks) | 0.4 IU | Standard Deviation 2.4 |
| Subetta | Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | Prandial insulin (36 weeks) | -1.6 IU | Standard Deviation 6.9 |
| Subetta | Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | Total daily dose insulin (36 weeks) | -1.2 IU | Standard Deviation 8.3 |
| Placebo | Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | Basal insulin (36 weeks) | 0.9 IU | Standard Deviation 2.9 |
| Placebo | Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | Prandial insulin (36 weeks) | -0.9 IU | Standard Deviation 4.5 |
| Placebo | Changes in Dosage of Insulin (Basal, Prandial and Total Daily Dose Insulin Measured in IU) | Total daily dose insulin (36 weeks) | 0.0 IU | Standard Deviation 6.2 |
Comparison: Analysis of basal insulin changes from baseline to Week 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.3107t-test, 2 sided
Comparison: Analysis of prandial insulin changes from baseline to Week 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.5236t-test, 2 sided
Comparison: Analysis of total daily dose insulin changes from baseline to Week 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.3847t-test, 2 sided
Secondary
Changes in Dosage of Total Insulin Measured in IU/kg of Body Weight
Insulin dose should be corrected by a patient on a daily basis taking into consideration data on blood glucose self- monitoring during a day and amount of food carbohydrates. Physician can correct insulin dose based on the same data.
Time frame: baseline and 36 weeks of the treatment
Population: Intention-to-Treat set
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Subetta | Changes in Dosage of Total Insulin Measured in IU/kg of Body Weight | -0.02 IU/kg | Standard Deviation 0.09 |
| Placebo | Changes in Dosage of Total Insulin Measured in IU/kg of Body Weight | -0.01 IU/kg | Standard Deviation 0.08 |
p-value: 0.6716t-test, 2 sided
Secondary
Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides)
Blood samples (for measurement of fasting plasma glucose, concentrations of plasma total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides) are taken under standard conditions: after night break in food taking (at least 12 hours) and prior to administering of insulin morning dose (prandial), prior to any morning medicines intake (including the study drug and permitted concomitant therapy).
Time frame: baseline and 12, 24 and 36 weeks of the treatment
Population: Intention-to-Treat set
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Total cholesterol (12 weeks) | 0.2 mmol / l | Standard Deviation 1 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Total cholesterol (24 weeks) | 0.1 mmol / l | Standard Deviation 1.1 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Total cholesterol (36 weeks) | 0.2 mmol / l | Standard Deviation 1 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | HDL cholesterol (12 weeks) | 0.1 mmol / l | Standard Deviation 0.3 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | HDL cholesterol (24 weeks) | 0.0 mmol / l | Standard Deviation 0.3 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | HDL cholesterol (36 weeks) | 0.1 mmol / l | Standard Deviation 0.3 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | LDL cholesterol (12 weeks) | 0.2 mmol / l | Standard Deviation 0.8 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | LDL cholesterol (24 weeks) | 0.0 mmol / l | Standard Deviation 0.9 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | LDL cholesterol (36 weeks) | 0.1 mmol / l | Standard Deviation 0.8 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Triglycerides (12 weeks) | -0.1 mmol / l | Standard Deviation 0.6 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Triglycerides (24 weeks) | -0.1 mmol / l | Standard Deviation 0.6 |
| Subetta | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Triglycerides (36 weeks) | -0.1 mmol / l | Standard Deviation 0.6 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Triglycerides (24 weeks) | 0.0 mmol / l | Standard Deviation 0.6 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Total cholesterol (12 weeks) | 0.2 mmol / l | Standard Deviation 0.9 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | LDL cholesterol (12 weeks) | 0.2 mmol / l | Standard Deviation 0.6 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Total cholesterol (24 weeks) | 0.4 mmol / l | Standard Deviation 1.2 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Triglycerides (12 weeks) | 0.1 mmol / l | Standard Deviation 0.8 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Total cholesterol (36 weeks) | 0.3 mmol / l | Standard Deviation 1.2 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | LDL cholesterol (24 weeks) | 0.3 mmol / l | Standard Deviation 0.9 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | HDL cholesterol (12 weeks) | 0.0 mmol / l | Standard Deviation 0.3 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | Triglycerides (36 weeks) | 0.1 mmol / l | Standard Deviation 0.8 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | HDL cholesterol (24 weeks) | 0.0 mmol / l | Standard Deviation 0.3 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | LDL cholesterol (36 weeks) | 0.3 mmol / l | Standard Deviation 0.9 |
| Placebo | Changes in Lipids (Concentrations of Plasma Total Cholesterol, HDL Cholesterol, LDL Cholesterol and Triglycerides) | HDL cholesterol (36 weeks) | 0.0 mmol / l | Standard Deviation 0.3 |
Comparison: Analysis of Total cholesterol changes from baseline to Week 12, 24 and 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.278Mixed Models Analysis
Comparison: Analysis of HDL cholesterol changes from baseline to Week 12, 24 and 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.8114Mixed Models Analysis
Comparison: Analysis of LDL cholesterol changes from baseline to Week 12, 24 and 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.1619Mixed Models Analysis
Comparison: Analysis of Triglycerides changes from baseline to Week 12, 24 and 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.0764Mixed Models Analysis
Secondary
Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data
The Diabetes Treatment Satisfaction Questionnaire allows to assess the degree of satisfaction with treatment for diabetes and its complications - retinopathy and nephropathy, how patients' satisfaction and perceived hyper- and hypoglycemia have changed compared to the initial period (before the treatment). The Diabetes Treatment Satisfaction Questionnaire contains six items scored on 7-point scales from +3 (equals very satisfied) to -3 (equals very dissatisfied), with 0 (equals no change). These are summed to produce a total Treatment Satisfaction score. Two questions concerning Perceived Hyperglycaemia and Perceived Hypoglycaemia respectively, are calculated separately. According to these two items, low scores represent good perceived blood glucose control (+3 means most of the time of Hyperglycaemia or Hypoglycaemia whereas -3 means none of the time of Hyperglycaemia or Hypoglycaemia).
Time frame: 36 weeks of the treatment
Population: Intention-to-Treat set. 6 patients (1 in the Subetta group and 5 in the Placebo group) was excluded from the analysis due to lake of questionnaires.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Subetta | Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | Satisfaction | 9.7 score on a scale | Standard Deviation 6.6 |
| Subetta | Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | Hyperglycemia | -0.7 score on a scale | Standard Deviation 1.5 |
| Subetta | Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | Hypoglycemia | -0.4 score on a scale | Standard Deviation 1.6 |
| Placebo | Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | Satisfaction | 8.4 score on a scale | Standard Deviation 6.5 |
| Placebo | Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | Hyperglycemia | -0.6 score on a scale | Standard Deviation 1.6 |
| Placebo | Satisfaction of Diabetes Treatment Based on Diabetes Treatment Satisfaction Questionnaire Data | Hypoglycemia | -0.6 score on a scale | Standard Deviation 1.4 |
Comparison: Analysis of total Treatment Satisfaction score at Week 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.2484t-test, 2 sided
Comparison: Analysis of Perceived Hyperglycaemia question at Week 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.761t-test, 2 sided
Comparison: Analysis of Perceived Hypoglycemia question at Week 36 endpoint between Subetta and Placebo treatment groups.p-value: 0.3714t-test, 2 sided