Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
study ends around

Description

Summary

The purpose of this study is to assess the efficacy and safety of barzolvolimab in adults with prurigo nodularis.

Official Title

A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Barzolvolimab (CDX-0159) in Patients With Prurigo Nodularis

Details

The purpose of this study is to assess the efficacy and safety of barzolvolimab (CDX-0159) in adults with prurigo nodularis.

There is a screening period of approximately 28 days, a 24-week double-blind treatment period and a 16-week follow-up period after treatment. Participants will be randomly assigned on a 1:1:1 ratio to receive barzolvolimab (CDX-0159) by subcutaneous injections of 150 mg every 4 weeks (Q4W) after an initial loading dose of 450 mg, 300 mg Q4W after an initial loading dose of 450 mg, or placebo Q4W.

Keywords

Prurigo Nodularis, barzolvolimab, PN, CDX-0159, Barzolvolimab 450 mg, then 150 mg Q4W, Barzolvolimab 450 mg, then 300 mg Q4W

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Males and females, ≥18 years of age.
  2. Diagnosis of Prurigo Nodularis by a dermatologist at least 3 months prior to

    Screening with:

    1. At least 20 PN nodules with bilateral distribution on both arms and/or both legs and/or both sides of the trunk at screening.
    2. An Investigators Global Assessment for stage of chronic nodular prurigo (IGA-CNPG-S) score for PN ≥ 3 at screening and Baseline (Day 1).
  3. Severe itch, defined as the mean of the daily worst itch NRS (WI-NRS) score of ≥ 7 during the 7-day period immediately prior to initiation of study treatment.
  4. Documented history of inadequate response to prescription topical medications or for whom topical medications are medically inadvisable.
  5. Willing to apply a topical moisturizer (emollient) once or twice a day throughout the study.
  6. Both males and females of child-bearing potential must agree to use highly effective contraceptives during the study and for 150 days afterwards after treatment.
  7. Willing and able to complete a daily symptom electronic diary for the duration of the study and adhere to the study visit schedule.

You CAN'T join if...

  1. PN due to neuropathy, psychiatric disorders or medications.
  2. Unilateral PN lesions limited to small area on one side of the body (e.g., only one arm affected).
  3. Active unstable pruritic skin conditions in addition to PN.
  4. Documented atopic dermatitis (moderate to severe) within 6 months before the start of screening.
  5. Females who are pregnant or nursing.
  6. Known hepatitis B or hepatitis C infection or active COVID-19 infection.
  7. Vaccination with a live vaccine within 2 months prior to study drug administration (subjects must agree to avoid vaccination during the study and for four months thereafter). NOTE: Inactivated vaccines are allowed such as seasonal influenza for injection. COVID-19 vaccination is allowed.
  8. History of anaphylaxis.
  9. Prior receipt of barzolvolimab

There are additional criteria that your study doctor will review with you to confirm you are eligible for the study.

Locations

  • University of California San Francisco accepting new patients
    San Francisco 5391959 California 5332921 94115 United States
  • Dermatology Institute & Skin Care Center accepting new patients
    Santa Monica 5393212 California 5332921 90404 United States
  • Focus Clinical Research accepting new patients
    West Hills 8030162 California 5332921 91307 United States
  • Profound Research LLC accepting new patients
    Oceanside 5378771 California 5332921 92056 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Celldex Therapeutics
ID
NCT06366750
Phase
Phase 2 Prurigo Nodularis Research Study
Study Type
Interventional
Participants
Expecting 120 study participants
Last Updated