NCT07598981Recruiting
PPDTM CorEvitasTM Obesity (OBR) Drug Effectiveness and Safety Registry
Source: ClinicalTrials.gov · Last updated 27 Aug 2026
Brief summary (registry, in English)
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
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 10000 (estimated)
- First submitted
- 28 Apr 2026
- Start date
- 29 Oct 2025
- Primary completion date
- 31 Dec 2099
- Lead sponsor
- CorEvitas
- Diseases
- Obesity
- NCT number
- NCT07598981
What you commit to
- Study type: Observational
- Planned participants: 10000
- From 29 Oct 2025 to the primary completion date, 31 Dec 2099
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Has Type 2 diabetes (T2D).
Other
- An individual who meets any of the following criteria will be excluded from participation in the registry:
- Is participating or planning to participate in a blinded clinical trial.
Who the study is looking for
- To be eligible to participate in this registry, an individual must meet all of the following criteria:
- 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.
- 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.
- Is willing and able to consent to participation in the registry.
- Is willing and able to complete registry-related forms electronically via personal devices
- Is willing and able to provide first name, last name, email address, language, and primary time zone for electronic data collection account creation.
- 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.
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CorEvitas, LLC Coordinator of this site? Confirm its status | Waltham | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.