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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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CorEvitas, LLC
Coordinator of this site? Confirm its status
WalthamUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.