A Prospective Observational Study of Patients Receiving Dupilumab for Prurigo Nodularis

Status: Active_not_recruiting
Location: See all (49) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This study is a prospective, multinational, observational investigation designed to elucidate the real-world effectiveness and treatment patterns of dupilumab therapy in adult patients diagnosed with prurigo nodularis (PN). The primary objective of this study is to comprehensively characterize the real-world usage of dupilumab for the management of PN. In addition to this, the study aims to achieve several secondary objectives, including a detailed assessment of the medical history, socio-demographic and disease characteristics of dupilumab-treated PN patients, as well as the evaluation of the long-term real-world effectiveness of dupilumab therapy for PN.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients aged 18 years or older at the time of informed consent.

• Physician decision to treat the patient with dupilumab for prurigo nodularis (according to the country-specific prescribing information) made prior to and independently of the patient's participation in the study.

• Patients able to understand and complete study-related questionnaires.

• Patients provide voluntary informed consent to participate in the study before inclusion in the study.

Locations
United States
Arizona
Medical Dermatology Specialists Site Number : 8400005
Phoenix
Saguaro Dermatology Associates, LLC - Probity - PPDS- Site Number : 8400024
Phoenix
California
Center for Dermatology Clinical Research- Site Number : 8400002
Fremont
Halcyon Dermatology- Site Number : 8400023
Laguna Hills
Mission Dermatology - Rancho Santa Margarita- Site Number : 8400015
Rancho Santa Margarita
Golden State Dermatology- Site Number : 8400014
Walnut Creek
Florida
Total Vein And Skin, LLC- Site Number : 8400019
Boynton Beach
GSI Clinical Research- Site Number : 8400017
Margate
Georgia
Allergy Center at Brookstone Research - Centricity Research - PPDS- Site Number : 8400025
Columbus
Indiana
Dawes Fretzin Clinical Research Group-7910 N Shadeland Ave- Site Number : 8400003
Indianapolis
Michigan
Oakland Hills Dermatology - 3400 Auburn Rd- Site Number : 8400007
Auburn Hills
Derm Institute of Western Michigan- Site Number : 8400034
Caledonia
Dermatology Associates Western Michigan- Site Number : 8400033
Grand Rapids
Missouri
U.S. Dermatology Partners Lee's Summit- Site Number : 8400016
Lee's Summit
North Carolina
Duke Dermatology Clinic- Site Number : 8400026
Durham
Nebraska
University of Nebraska - Lauritzen Outpatient Center- Site Number : 8400029
Omaha
Nevada
Las Vegas Dermatology- Site Number : 8400027
Las Vegas
Vivida Dermatology - Flamingo- Site Number : 8400013
Las Vegas
South Carolina
Medical University of South Carolina (MUSC) - PPDS- Site Number : 8400001
Charleston
Texas
North Texas Center for Clinical Research- Site Number : 8400012
Frisco
U.S. Dermatology Partners Longview- Site Number : 8400032
Longview
Texas Tech University Health Sciences Center-125 W Hague Rd- Site Number : 8400010
Lubbock
West Virginia
West Virginia Research Institute- Site Number : 8400030
Morgantown
Other Locations
Canada
Investigational Site Number : 1240004
Ajax
Investigational Site Number : 1240003
Barrie
Investigational Site Number : 1240009
Calgary
Investigational Site Number : 1240007
Edmonton
Investigational Site Number : 1240006
Fredericton
Investigational Site Number : 1240011
London
Investigational Site Number : 1240002
Newmarket
Investigational Site Number : 1240012
Surrey
Investigational Site Number : 1240005
Toronto
Investigational Site Number : 1240010
Waterloo
China
Investigational Site Number : 1560005
Beijing
Investigational Site Number : 1560007
Beijing
Investigational Site Number : 1560009
Guangzhou
Investigational Site Number : 1560008
Hangzhou
Investigational Site Number : 1560003
Jinan
Investigational Site Number : 1560006
Shanghai
Investigational Site Number : 1560002
Shenzhen
Investigational Site Number : 1560010
Wenzhou
Investigational Site Number : 1560004
Xi'an
France
Investigational Site Number : 2500005
Brest
Investigational Site Number : 2500001
Nantes
Japan
Investigational Site Number : 3920003
Kyoto
Investigational Site Number : 3920004
Matsudo
Investigational Site Number : 3920001
Obihiro
Netherlands
Investigational Site Number : 5280001
Bergen Op Zoom
Investigational Site Number : 5280002
Hoofddorp
Time Frame
Start Date: 2023-12-12
Completion Date: 2026-09-22
Participants
Target number of participants: 100
Treatments
Patient with prurigo nodularis
Participants aged 18 years or older who start receiving dupilumab for prurigo nodularis (according to the country-specific prescribing information) prior to and independently of their participation in the study
Related Therapeutic Areas
Sponsors
Collaborators: Regeneron Pharmaceuticals
Leads: Sanofi

This content was sourced from clinicaltrials.gov