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RECRUITING
NCT07276425

Early and Long-Term Efficacy and Immune Changes With Dupilumab in Prurigo Nodularis

Sponsor: UMC Utrecht

View on ClinicalTrials.gov

Summary

With the arrival of dupilumab as the first available targeted therapy for PN, there is an unmet need for real-world data and translational research on the working mechanism of dupilumab on PN, to optimize individualized targeted treatment.

Official title: Early and Long-term Clinical Efficacy and Local Tissue and Peripheral Immune Changes Following Dupilumab Treatment in Prurigo Nodularis Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

40

Start Date

2025-06-01

Completion Date

2028-06-01

Last Updated

2025-12-18

Healthy Volunteers

No

Interventions

DRUG

Dupilumab

In the Netherlands, the standard care for patients with moderate-to-severe prurigo nodularis who have failed or are contraindicated to conventional systemic immunosuppressive treatments consists of 300 mg of dupilumab administered subcutaneously every two weeks, following a loading dose of 600 mg administered subcutaneously.

Locations (1)

University Medical Center Utrecht

Utrecht, Utrecht, Netherlands