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NCT Number: NCT06100991

CorEvitas Generalized Pustular Psoriasis (GPP) Drug Safety and Effectiveness Registry

Prospective, observational registry for subjects with GPP under the care of a dermatology investigator.Approximately 200 subjects and 75 clinical sites in North America will be recruited to participate with no defined upper limit for either target

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CorEvitas, LLC

Waltham, Massachusetts, 02451, United States

Location status: Recruiting

Location contact

Cathy Cheney

CONTACT

[email protected]

About this study

The objective of the registry is to obtain information on the treatment patterns, disease activity progression, and the development of comorbidities and adverse events in a cohort of patients with GPP. Data collected will be used to better characterize the natural history and longitudinal trajectory of the disease. This will be done through the standardized data collection including validated patient-reported outcomes (PRO) and clinician-reported outcomes (ClinRO), the active evaluation of prevalent and incident comorbidities and adverse events, and the recording of medication utilization patterns. Personal information is also collected from each consenting registry subject allowing for linkages to other public or private clinical and administrative databases, as well as to databases maintained by organizations focused on the care and treatment of GPP for the purposes of clinical, market, or outcomes research.

This provides an opportunity to evaluate other aspects of the disease and its treatment, including but not limited to clinical and drug cost-effectiveness, health care resource utilization, and subject adherence.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • A subject must meet all the following criteria to participate in the registry:
  • Has been diagnosed with GPP by a dermatologist or a qualified dermatology practitioner.
  • Is at least 18 years of age and has attained the legal age for consent to procedures involved in the research, under the applicable law of the jurisdiction in which the research is being conducted.
  • Is willing to provide consent for participation in the registry.
  • Is willing to provide Personal Information

Exclusion criteria

  • Any of the following would exclude the subject from participating in the registry:
  • Is participating or planning to participate in a blinded clinical trial evaluating a systemic agent for the treatment or prevention of flares related to GPP.
  • Is enrolled in another CorEvitas registry for a dermatological condition. Subjects enrolled in another CorEvitas registry must be exited to be eligible for enrollment into the GPP Registry

Treatment and study plan

Primary outcomes

  1. Primary Outcome Measure:GPP epidemiology and Presentation

    Time frame: Through study completion, an average of 10 years

    The major clinical outcomes include an assessment of the epidemiology of GPP; to better understand the presentation and natural history.

  2. GPP management, and outcomes

    Time frame: Through study completion, an average of 10 years

    The major clinical outcome include an assessment of the epidemiology of GPP; to better understand the management and outcomes.

Study contacts

Contact information is provided by the study sponsor or research team.

Cathy Cheney

CONTACT

[email protected]

+1 508 408 5433

Jeffrey Greenberg, MD

CONTACT

Sponsors and collaborators

Lead sponsor

CorEvitas

Network

Registry information

Important dates

Study start
2023
Primary completion
2099
Study completion
2099
First posted
Oct 25, 2023
Registry last updated
Feb 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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