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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06366750 on ClinicalTrials.gov