Clinical Research Directory
Browse clinical research sites, groups, and studies.
PPD™ CorEvitas™ Psoriasis (PSO) Early Treatment Response Non-Interventional Study
Sponsor: CorEvitas
Summary
This is a 24-week prospective, single-arm cohort, study of patients initiating advanced therapy for the treatment of moderate-to-severe plaque PSO. Eligible patients must be willing to be seen in-person by their treating physician for a Baseline visit (with first dose of the advanced therapy occurring within 14 days), and at 16 (+/- 5 days) and 24 weeks (+14 days) calculated based on date of first dose of the advanced therapy and must provide informed consent prior to enrolling in the study or completing study-specific questionnaires or procedures. Data will be collected from both subjects and their treating dermatology provider at predetermined scheduled intervals (Baseline, Week 16 and Week 24) using a structured and standardized data collection tool.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
2500
Start Date
2026-06-01
Completion Date
2036-12-31
Last Updated
2026-08-26
Healthy Volunteers
Yes
Conditions
Interventions
Observational (Non-Interventional) Registry
This is an observational (non-interventional) registry
Locations (1)
CorEvitas, LLC
Waltham, Massachusetts, United States