Recruiting

Observational Study

Sponsor:

CorEvitas

Code:

NCT07598981

Conditions

Obesity

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Biospecimen collection

Study Details

Brief summary:

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

Conditions

Obesity

Study ID

NCT07598981

Start date

Oct 29, 2025

Status verified date

Jan, 2026

Completion date

Dec 31, 2099

Anticipated

Primary completion date

Dec 31, 2099

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

To be eligible to participate in this registry, an individual must meet all of the following criteria:

1. In the opinion of the investigator, the subject is considered a suitable candidate for treatment with a commercially available systemic obesity medication (see Enrollment Eligible Treatments). While subjects do not need to start an obesity medication at the time of registry enrollment, those prescribed a GLP-based or non-GLP-based obesity medication must be initiating the medication for the first time.
2. Is at least 18 years of age or older and has attained the legal age for consent to procedures involved in the research, under the applicable laws of the jurisdiction in which the research is being conducted at the time of enrollment.
3. Is willing and able to consent to participation in the registry.
4. Is willing and able to complete registry-related forms electronically via personal devices
5. Is willing and able to provide first name, last name, email address, language, and primary time zone for electronic data collection account creation.
6. For US subjects only, is willing and able to provide Personally Identifiable Information which includes full legal name, sex at birth, date of birth, and home address zip code.

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in the registry:

1. Has Type 2 diabetes (T2D).
2. Is participating or planning to participate in a blinded clinical trial.

Study Design

Enrollment

10000 participants

Anticipated

Interventions and Outcome Measures

Interventions

Biospecimen collection

Blood Samples will be collected from subjects. This is optional for the participating subjects

Primary outcome measure

  • Obesity Epidemiology and presentation [ Time Frame: Every 6 months for 10 years ]

Central Contacts and Locations

Central contacts

Locations

CorEvitas, LLC

Recruiting

Waltham, Massachusetts, United States, 02451

Contacts

More Information

Sponsor

CorEvitas

Last update posted

Aug 27, 2026

Last verified

Jan, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by CorEvitas on 2026-08-27.