Spartina® (Tirzepatide) Effectiveness and Safety Evaluation
Trial Parameters
Brief Summary
The goal of this study is to evaluate Effectiveness and safety of Spartina® (Tirzepatide) in male or female participants with obesity and overweight. The main questions which are aimed to be answered: 1. Is Spartina® (Tirzepatide) effective in the treatment of obesity and overweight? 2. Is Spartina® (Tirzepatide) safe in the treatment of obesity and overweight? In this study, there is no comparison group. Participants receive Spartina® (Tirzepatide)
Eligibility Criteria
Inclusion Criteria: 1. Male or female ≥18 years of age 2. Willingness for signing and having signed the informed consent form 3. BMI ≥30 kg/m² or ≥27 kg/m² with ≥1 weight-related comorbidity Exclusion Criteria: 1. Prior use of any GLP-1 agonist in the last 6 months 2. Type 1 diabetes mellitus 3. Any condition or circumstance that might pose a risk to the subject or interfere with the ability to acquire satisfactory clinical data 4. Pregnancy or breast-feeding 5. Personal or family history of medullary thyroid carcinoma (MTC) or patients with multiple endocrine neoplasia syndrome type 2 (MEN 2)