BK329 and Body Fat Reduction (NCT06628791) | Clinical Trial Compass
CompletedNot Applicable
BK329 and Body Fat Reduction
South Korea100 participantsStarted 2024-01-26
Plain-language summary
This clinical trial aims to determine whether BK329 reduces body fat in adults with overweight or obesity and to assess its safety.
The main questions are:
* Does BK329 reduce body fat in participants?
* What side effects occur when participants take BK329?
Who can participate
Age range19 Years – 75 Years
SexALL
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Inclusion Criteria:
* individuals with a Body Mass Index (BMI) between 23 and 30 kg/m2.
* Individuals who have provided written consent on the consent form.
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 ha…