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 Francisco
accepting new patients
San Francisco California 94115 United States - University of California, San Francisco
accepting new patients
San Francisco California 94115 United States - Dermatology Institute & Skin Care Center
accepting new patients
Santa Monica California 90404 United States - Focus Clinical Research
accepting new patients
West Hills California 91307 United States - Profound Research LLC
accepting new patients
Oceanside California 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
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study, which might include an external sponsor. Providing your contact details does not obligate you to participate in the research.
Thank you!
The study team should get back to you in a few business days.