Efficacy and Safety of Akkermansia Muciniphila AKM Lab-01 for Overweight and Obesity

Prior treatment

• 3\) Concurrent severe medical conditions deemed by the investigator to require immediate treatment, such as severe diabetes mellitus, hypertriglyceridemia, or cerebrovascular disease.
• 4\) Concurrent severe primary diseases of the liver, kidney, or hematopoietic system; or individuals with mental illness.
• 6\) Participants currently taking hepatotropic medications.
• 7\) Participants with a history of prior bariatric surgery.
• 13\) Know hypersensitivity or allergy to any active ingredient or excipient of the investigational product.
• 14\) Use of antibiotic therapy or intake of probiotics/prebiotic supplements within 3 month prior to screening.

Other illness

• 1\) A clear history of neurological or psychiatric disorders (including epilepsy and dementia).
• 2\) Hyperlipidemia due to secondary causes, such as nephrotic syndrome, hepatic diseases, hypothyroidism, or renal failure.
• 5\) Participants with a family history of genetically inherited metabolic disorders.
• 8\) Presence of poorly controlled or unstable acute/chronic diseases, including but not limited to:
  • Cardiovascular diseases: Unstable angina, myocardial infarction within the past 6 months, symptomatic congestive heart failure (NYHA Class Ⅱ or higher), severe arrhythmia, ect.
  • Uncontrolled active infectious diseases, malignancies, ect.
• 11\) History of acute diabetic complications (e.g., diabetic ketoacidosis or hyperosmolar hyperglycemic state) within the past 3 months.
• 12\) History of gastrointestinal surgery within the past year, or the presence of severe, active gastrointestinal disease that is not stabilized and may affect drug absorption, distribution, metabolism, or excretion.
• 17\) Any other medical condition that, in the judgement of the investigator, may put the participant at increased or be aggravated by participation in the study. The specific reason for exclusion based on this criterion must be documented.

Lab values

• 9\) Participants with hepatic or renal insufficiency, defined as:
  • Alanine aminotransferase (ALT) or Aspartate aminotransferase (AST) \> 2.5 × ULN (Upper Limit of Normal);
  • Serum total bilirubin \> 2.5 × ULN;
  • Creatinine (Cr) \> 1.5 × ULN.
• 10\) Urine amylase ≥ 1.5 × ULN, or any other laboratory abnormality deemed by the investigator to be clinically significant and incompatible with study participation.

Other

• 15\) Excessive alcohol consumption (defined as \> 30 grams per day for men or \> 20 gram, sraems) with the past 10 years.
• 16\) pregnant or lactating women.

• 1\) Age: 18-60 years old (inclusive); Gender: male or female.
• 2\) Body Mass Index (24.0≤BMI≤40.0 kg/m²).
• 3\) Has no taken any medications for metabolic control (e.g., for body weight, blood lipids, or blood glucose) within the past month.
• 4\) Has been attempting to manage weight primarily through lifestyle interventions (diet and exercise) for at least one month prior to screening.
• 5\) Processes adequate communication and cognitive abilities, is expected to be compliant with long-term medication, and has understood the nature, significance, potential benefits, inconveniences, and risks of the study prior to enrollment.
• 6\) For participants of childbearing potential (male or female): Must agree to use at least one medically approved form of contraception (e.g., intrauterine device \[IUD\], oral contraceptives, or condoms) throughout the trial. For female participants of childbearing potential: Must have a negative serum pregnancy test at screening and must be non-lactating.
• 7\) Voluntarily agrees to participate by signing the inform consent form and commits to follow the trial treatment plan and visit schedule.