BK329 and Body Fat Reduction

Exclusion Criteria

• •Subjects with severe cerebrovascular disease (e.g., stroke, cerebral hemorrhage), heart disease (e.g., angina, myocardial infarction, heart failure, arrhythmia requiring treatment), or malignant tumors within the last 6 months. (However, subjects with a history of these diseases who are clinically stable may participate at the investigator's discretion.)
• •Uncontrolled hypertensive patients (blood pressure ≥160/100mmHg, measured after 10 minutes of rest).
• •Diabetic patients with poor blood glucose control (fasting glucose ≥160mg/dL).
• •Subjects undergoing treatment for hypothyroidism or hyperthyroidism.
• •Subjects with creatinine levels ≥ 2 times the upper limit of the research institution's normal range.
• •Subjects with aspartate transaminase or alanine transaminase levels ≥ 3 times the upper limit of the research institution's normal range.
• •Subjects experiencing severe gastrointestinal symptoms such as heartburn or indigestion (lactose intolerance).
• •Subjects who have taken weight-altering drugs (absorption inhibitors, appetite suppressants, obesity-related supplements, psychiatric drugs, beta-blockers, diuretics, contraceptives, steroids, or female hormones) within the last month.
• •Subjects who have participated in commercial weight loss programs within the last 3 months.
• •Subjects who have participated in or plan to participate in another clinical trial within the last month.
• •Alcohol abusers.
• •Subjects who quit smoking within the last 3 months.
• •Pregnant or breastfeeding women or those planning pregnancy during the trial period.
• •Subjects with allergies to any components of the study foods.
• •Subjects deemed inappropriate for the study by the investigator for other reasons.