National, Multicenter, Randomized, Double-blind, Triple-dummy, Phase III Clinical Trial to Evaluate the Efficacy and Safety of Berlim 25/20 Association in the Treatment of Type II Diabetes Mellitus and Dyslipidemia.
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 228
- 试验地点
- 1
- 主要终点
- Reduction of glycated hemoglobin levels measured between the first visit and the last visit.
研究概览
简要总结
The purpose of this study is to evaluate the efficacy and safety of Berlim 25/20 association in the treatment of type 2 diabetes mellitus and dyslipidemia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Ability to confirm voluntary participation and agree to all trial purposes by signing and dating the informed consent forms;
- •Participants of both sexes, with age greater than or equal to 18 years and less than or equal to 85 years;
- •Participants presenting the diagnosis of type II diabetes mellitus, and who did not reach the therapeutic goals of HbA1c with previous dietary, physical exercise guidance and previous therapies at a stable dose in the last 3 months;
- •HbA1c ≥ 7,5% and ≤ 10,5% and fasting blood glucose > 100 mg/dL at the screening visit;
- •Participants with high or very high cardiovascular risk according to the Brazilian guideline on the prevention of cardiovascular diseases in patients with diabetes (2017), which have not reached the goal of LDL-c ≤ 70 mg/dL or ≤ 50 mg/dL, respectively, with lifestyle changes, who are or aren't using low or moderate potency statins;
- •BMI (body mass index) > 19 Kg/m2 and ≤ 45 Kg/m2.
排除标准
- •Any clinical and laboratory findings that, in the judgment of the investigator, may interfere with the safety of research participants;
- •History of alcohol abuse or illicit drug use;
- •Participation in a clinical trial in the year prior to this study;
- •Pregnancy or risk of pregnancy and lactating patients;
- •Known hypersensitivity to the formula components used during the clinical trial;
- •Type 1 diabetes mellitus;
- •Fasting blood glucose > 300 mg/dL;
- •Risk factors for volume depletion;
- •Participants with total cholesterol > 500 mg/dL or triglycerides > 500 mg/dL;
- •Impaired renal function and end-stage renal disease;
- •Participants with known heart failure, class III to IV (New York Heart Association);
- •Impaired hepatic function;
- •Medical history of pancreatic diseases that may suggest insulin deficiency;
- •Participants who had any cardiovascular event (acute myocardial infarction, acute coronary syndrome, recent onset stable angina, stroke, unstable congestive heart failure requiring treatment change), underwent revascularization or vascular surgery in the 6 months prior to screening;
- •Bariatric surgery in the last two years and/ or other gastrointestinal surgeries that can cause chronic malabsorption syndrome;
- •Condition that, in the investigator's judgment, may favor clinically significant changes in CPK levels;
- •Current medical history of cancer and/ or cancer treatment in the last 5 years;
- •Participants with known uncontrolled hypothyroidism or TSH levels > 5 mIU/L;
- •History of known muscle disease or prior statin intolerance;
- •Participants using SGLT2 inhibitors, sulfonylureas and/or insulin therapy or PCSK9 inhibitors;
- •Participants who used other medications with prominent action in the control of serum triglyceride and cholesterol levels in the last 4 weeks or who are using low or moderate-intensity statins that cannot be replaced by rosuvastatin 20 mg;
- •Participants using medications that may interfere with triglyceride and cholesterol metabolism started less than 4 weeks ago or with dose adjustment in the last 4 weeks prior to the screening visit;
- •Treatment with anti-obesity drugs for less than 2 months or with dose change in the last 2 months.
研究组 & 干预措施
BERLIM 25/20
The study is triple-dummy. The patient must take 3 tablets once a day, as follows:
1 tablet Berlim 25/20 association, oral;
1 tablet empagliflozin placebo, oral;
1 tablet rosuvastatin calcium placebo, oral.
干预措施: BERLIM 25/20 ASSOCIATION (Drug)
BERLIM 25/20
The study is triple-dummy. The patient must take 3 tablets once a day, as follows:
1 tablet Berlim 25/20 association, oral;
1 tablet empagliflozin placebo, oral;
1 tablet rosuvastatin calcium placebo, oral.
干预措施: EMPAGLIFLOZIN PLACEBO (Other)
BERLIM 25/20
The study is triple-dummy. The patient must take 3 tablets once a day, as follows:
1 tablet Berlim 25/20 association, oral;
1 tablet empagliflozin placebo, oral;
1 tablet rosuvastatin calcium placebo, oral.
干预措施: ROSUVASTATIN CALCIUM PLACEBO (Other)
Empagliflozin + rosuvastatin calcium
The patient must take 3 tablets once a day, as follows:
1 tablet Berlim 25/20 association placebo, oral;
1 tablet empagliflozin, oral;
1 tablet rosuvastatin calcium, oral.
干预措施: EMPAGLIFLOZIN (Drug)
Empagliflozin + rosuvastatin calcium
The patient must take 3 tablets once a day, as follows:
1 tablet Berlim 25/20 association placebo, oral;
1 tablet empagliflozin, oral;
1 tablet rosuvastatin calcium, oral.
干预措施: ROSUVASTATIN CALCIUM (Drug)
Empagliflozin + rosuvastatin calcium
The patient must take 3 tablets once a day, as follows:
1 tablet Berlim 25/20 association placebo, oral;
1 tablet empagliflozin, oral;
1 tablet rosuvastatin calcium, oral.
干预措施: BERLIM 25/20 ASSOCIATION PLACEBO (Other)
结局指标
主要结局
Reduction of glycated hemoglobin levels measured between the first visit and the last visit.
时间窗: 120 days
Percentual reduction of LDL-c levels measured between the first visit and the last visit.
时间窗: 120 days
次要结局
- Incidence and severity of adverse events recorded during the study.(150 days)