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This observational study is designed to assess the effects of Envlo Tablet or Envlomet SR Tablet on weight loss and safety in patients with Type 2 diabetes, conducted in real primary care settings over a period of 24 weeks.
The study plans to recruit patients with Type 2 diabetes who are scheduled to receive Envlo Tablet or Envlomet SR Tablet based on the attending physician's medical judgment, regardless of previous diabetes treatment. However, voluntary consent from patients is required for participation in the study, even if Envlo Tablet or Envlomet SR Tablet are prescribed.
Data collection will occur for up to 24 weeks post-Envlo Tablet or Envlomet SR Tablet initiation, capturing demographic information, physical measurements, vital signs, and lifestyle factors. Follow-up visits at 12 weeks and 24 weeks post-baseline will be conducted to collect data, including clinical indicators, safety evaluations, and adverse events. Data will be collected based on routine clinical records, with no mandatory study-specific visits or interventions.
Overall, this observational study aims to collect data on demographics, physical measurements, vital signs, and clinical indicators in patients receiving Envlo Tablet or Envlomet SR Tablet in real-world clinical settings, utilizing information obtained during routine patient care processes.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| patient diagnosed with type2 diabetes mellitus | patient diagnosed with type2 diabetes mellitus |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Envlo Tablet | Drug | Enavogliflozin 0.3mg |
| |
| Measure | Description | Time Frame |
|---|---|---|
| change in BMI | change in BMI at 24 weeks from baseline | 24 weeks |
| change in body weight | change in body weight at 24 weeks from baseline | 24 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| change in BMI | change in BMI at 12 weeks from baseline | 12 weeks |
| change in body weight | change in body weight at 12 weeks from baseline |
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Inclusion Criteria:
Adults aged 19 to 80 years.
Patients with Type 2 diabetes who are scheduled to receive initial treatment with Enavogliflozin or Enavogliflozin Extended-Release Tablets based on the attending physician's medical judgment, within the following insurance coverage ranges:
Patients with obesity beyond the pre-obesity stage according to the 2022 Korean Endocrine Society obesity treatment guidelines:
Individuals planning to undertake appropriate exercise and dietary therapy for glycemic control during the observational study period.
Fertile women and men who agree to contraception according to appropriate contraceptive methods during the observational study period or have no plans for pregnancy, adhering to methods such as hormonal contraceptives, intrauterine devices or systems, tubal ligation, vasectomy, dual contraception methods (such as cervical cap and male condom), etc.
Individuals who have received detailed explanation and have understood the nature of the observational study and the investigational drug, and have provided written consent to participate voluntarily in the observational study and to comply with subject precautions during the study period.
Exclusion Criteria:
Individuals with diabetes other than Type 2 diabetes (Type 1 diabetes, diabetic ketoacidosis, gestational diabetes, etc.).
Individuals contraindicated for Enavogliflozin or Enavogliflozin Extended-Release Tablets based on the approved indications:
Patients initiating treatment with Enavogliflozin or Enavogliflozin Extended-Release Tablets at enrollment with an eGFR of less than 60 mL/min/1.73m2.
Patients with unstable weight due to treatment with obesity drugs or weight loss medications within 3 months prior to enrollment or other treatments (surgery, dietary therapy, etc.).
Individuals with diminished mental capacity.
Pregnant and lactating women.
Individuals currently participating in another clinical trial and receiving investigational drugs or investigational medical devices.
Other individuals deemed unsuitable for participation in the observational study based on the investigator's (attending physician's) judgment.
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The mean and standard deviation of the change from baseline to 12 or 24 weeks in weight and body mass index (BMI) from previously conducted Phase 2 and Phase 3 clinical trials were used as references for calculation using G*Power 3.1.9.7.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Kyung Hee University Medical Center | Seoul | South Korea |
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| Envolomet SR Tablet |
| Drug |
Enavogliflozin 0.3mg/Metformin1,000mg |
|
| 12 weeks |
| Proportion of subjects achieving ≥ 5% reduction in BMI | Proportion of subjects achieving ≥ 5% reduction in BMI at 12 weeks compared to baseline | 12 weeks |
| Proportion of subjects achieving ≥ 5% reduction in BMI | Proportion of subjects achieving ≥ 5% reduction in BMI at 24 weeks compared to baseline | 24 weeks |
| Proportion of subjects achieving ≥ 5% reduction in weight | Proportion of subjects achieving ≥ 5% reduction in weight at 12 weeks compared to baseline | 12 weeks |
| Proportion of subjects achieving ≥ 5% reduction in weight | Proportion of subjects achieving ≥ 5% reduction in weight at 24 weeks compared to baseline | 24 weeks |
| Change in body composition analyzer indicators (body fat mass, visceral fat mass, muscle mass, waist/hip circumference, etc.) | Change in body composition analyzer indicators (body fat mass, visceral fat mass, muscle mass, waist/hip circumference, etc.) at 12 weeks compared to baseline | 12 weeks |
| Change in body composition analyzer indicators (body fat mass, visceral fat mass, muscle mass, waist/hip circumference, etc.) | Change in body composition analyzer indicators (body fat mass, visceral fat mass, muscle mass, waist/hip circumference, etc.) at 24 weeks compared to baseline | 24 weeks |
| Change in HbA1c | Change in HbA1c at 12 weeks compared to baseline | 12 weeks |
| Change in HbA1c | Change in HbA1c at 24 weeks compared to baseline | 24 weeks |
| Change in FPG | Change in FPG at 12 weeks compared to baseline | 12 weeks |
| Change in FPG | Change in FPG at 24 weeks compared to baseline | 24 weeks |
| Proportion of subjects achieving HbA1c < 7% | Proportion of subjects achieving HbA1c < 7% at 12 weeks compared to baseline | 12 weeks |
| Proportion of subjects achieving HbA1c < 7% | Proportion of subjects achieving HbA1c < 7% at 24 weeks compared to baseline | 24 weeks |
| Proportion of subjects achieving HbA1c < 6.5% | Proportion of subjects achieving HbA1c < 6.5% at 12 weeks compared to baseline | 12 weeks |
| Proportion of subjects achieving HbA1c < 6.5% | Proportion of subjects achieving HbA1c < 6.5% at 24 weeks compared to baseline | 24 week |
| Proportion of subjects achieving therapeutic response [change in HbA1c (baseline HbA1c - HbA1c at each evaluation time point) > 0.5% or HbA1c < 7%] | Proportion of subjects achieving therapeutic response [change in HbA1c (baseline HbA1c - HbA1c at each evaluation time point) > 0.5% or HbA1c < 7%] at 12 weeks compared to baseline | 12 weeks |
| Proportion of subjects achieving therapeutic response [change in HbA1c (baseline HbA1c - HbA1c at each evaluation time point) > 0.5% or HbA1c < 7%] | Proportion of subjects achieving therapeutic response [change in HbA1c (baseline HbA1c - HbA1c at each evaluation time point) > 0.5% or HbA1c < 7%] at 24 weeks compared to baseline | 24 weeks |
| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
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