A Study of Barzolvolimab in Patients With Prurigo Nodularis
NCT06366750 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 140
Last updated 2026-01-30
Summary
The purpose of this study is to assess the efficacy and safety of barzolvolimab in adults with prurigo nodularis.
Conditions
- Prurigo Nodularis
Interventions
- BIOLOGICAL
-
barzolvolimab
subcutaneous administration
- OTHER
-
Matching Placebo
subcutaneous administration
Sponsors & Collaborators
-
Celldex Therapeutics
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-04-12
- Primary Completion
- 2026-06-30
- Completion
- 2027-03-31
- FDA Drug
- Yes
Countries
- United States
- Canada
- Croatia
- Germany
- Poland
- Spain
Study Locations
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