A Study of Barzolvolimab in Patients With Prurigo Nodularis
a study on Prurigo Nodularis
Summary
- Eligibility
- for people ages 18 years and up (full criteria)
- Location
- at UCSF
- Dates
- study startedstudy 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
- Males and females, ≥18 years of age.
- Diagnosis of Prurigo Nodularis by a dermatologist at least 3 months prior to - Screening with: - At least 20 PN nodules with bilateral distribution on both arms and/or both legs and/or both sides of the trunk at screening.
- An Investigators Global Assessment for stage of chronic nodular prurigo (IGA-CNPG-S) score for PN ≥ 3 at screening and Baseline (Day 1).
 
- 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.
- Documented history of inadequate response to prescription topical medications or for whom topical medications are medically inadvisable.
- Willing to apply a topical moisturizer (emollient) once or twice a day throughout the study.
- 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.
- 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...
- PN due to neuropathy, psychiatric disorders or medications.
- Unilateral PN lesions limited to small area on one side of the body (e.g., only one arm affected).
- Active unstable pruritic skin conditions in addition to PN.
- Documented atopic dermatitis (moderate to severe) within 6 months before the start of screening.
- Females who are pregnant or nursing.
- Known hepatitis B or hepatitis C infection or active COVID-19 infection.
- 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.
- History of anaphylaxis.
- 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 Franciscoaccepting new patients 
 San Francisco 5391959 California 5332921 94115 United States
- Dermatology Institute & Skin Care Centeraccepting new patients 
 Santa Monica 5393212 California 5332921 90404 United States
- Focus Clinical Researchaccepting new patients 
 West Hills 8030162 California 5332921 91307 United States
- Profound Research LLCaccepting 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
