The design is an open-ended prospective observational (non-interventional) registry for subjects living with excess weight or obesity under the care of a qualified provider with documented experience treating patients with obesity
The objective of the registry is to create a cohort of subjects living with excess weight or obesity to evaluate long-term real-world effectiveness and safety of standard of care treatments for obesity. Data collected through the registry may be used to address a range of research questions and use cases, including but not limited to: characterizing the natural history of the disease, evaluating the effectiveness and safety of commercially available medications for the treatment of obesity, providing information to support ongoing risk-benefit evaluation by drug manufacturers and regulators, and research related to drug utilization, disease burden, and unmet needs.
Study Type
OBSERVATIONAL
Enrollment
10,000
Blood Samples will be collected from subjects. This is optional for the participating subjects
CorEvitas, LLC
Waltham, Massachusetts, United States
Obesity Epidemiology and presentation
The major clinical outcome include an assessment of the epidemiology of Obesity. This will be determined using PROs and ClinROs which will be included as part of the case report forms.
Time frame: Every 6 months for 10 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.