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Clinical Trials in the UK / NCT07266402
Recruiting Phase 3

A Study to Investigate Efficacy, Safety and Tolerability of Barzolvolimab Versus Placebo in Adults With Cold Induced Urticaria and Symptomatic Dermographism Inadequately Controlled by H1-antihistamines (EMBARQ - ColdU and SD)

NCT07266402 · tracked via the Priya Life Science UK tracker
Sponsor
Celldex Therapeutics
Phase
Phase 3
Started
2026-01-15
Last updated
2026-08-26

Condition(s) studied

Chronic Inducible UrticariaCold UrticariaCold-Induced UrticariaSymptomatic Dermographism

Investigational drug(s) / intervention(s)

BarzolvolimabMatching Placebo

Barzolvolimab: Subcutaneous Administration

Matching Placebo: Subcutaneous Administration

Study summary

The purpose of this Phase 3, randomized, double-blind, placebo-controlled study is to assess the activity and safety of barzolvolimab compared to placebo in participants with cold induced urticaria or symptomatic dermographism who remain symptomatic despite the use of H1-antihistamines.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: 1. Males and females, \>/= 18 years of age. 2. Diagnosis of cold induced urticaria or symptomatic dermographism \>/= 3 months. 3. Diagnosis of cold induced urticaria or symptomatic dermographism despite the use of a stable regimen of second generation non-sedating H1-antihistamine as defined by: 1. The presence of hives for \>/= 6 weeks at any time prior to Visit 1 despite the use of H1-antihistamines. 2. Must be on a stable regimen of second generation non-sedating H1-antihistamine for \>/= 4 weeks prior to study treatment. 3. Cold induced urticaria: A Critical Threshold Temperature (CTT) of ≥ 15 °C and \< 37 °C using the TempTest® and a numerical rating scale score of ≥ 5 for itch after the provocation test. 4. Symptomatic dermographism: A Critical Friction Threshold (CFT) of ≥ 3 using the FricTest® and a numerical rating scale score of ≥ 5 for itch after the provocation test. 4. Cold induced urticaria: Positive ice-cube test resulting in hives at the provocation site during Screening 5. Normal blood counts and liver function tests. 6. Both males and females of child-bearing potential must agree to use highly effective contraceptives during the study and for ≥ 150 days after treatment. 7. Willing and able to complete a daily symptom electronic diary and comply with study visits. 8. Participants with and without prior biologic experience are eligible. Key Exclusion Criteria: 1. Women who are pregnant or nursing. 2. Clearly defined cause for chronic urticaria. 3. Active, pruritic skin condition in addition to cold induced urticaria or symptomatic dermographism. 4. Medical condition that would cause additional risk or interfere with study procedures. 5. Known HIV, hepatitis B or hepatitis C infection. 6. Vaccination with a live vaccine within 30 days prior to screening (subjects must agree to avoid vaccination with a live vaccine during the study). Inactivated vaccines are allowed such as seasonal influenza injection or COVID-19 vaccine. 7. History of anaphylaxis, unless due to cold exposure over a large part of the body (such as swimming in cold water). 8. Prior treatment with barzolvolimab There are additional criteria that your study doctor will review with you to confirm you are eligible for the study.

Primary outcome measure(s)

Trial sites (72)

FacilityCityRegionStatus
Cahaba Dermatology & Skin Health Center, LLC Birmingham Alabama Recruiting
One of a Kind Clinical Research Center, LLC Scottsdale Arizona Recruiting
Kern Research, Inc. Bakersfield California Recruiting
One of a Kind Clinical Research Center Napa California Recruiting
Allergy & Asthma Consultants Redwood City California Recruiting
Amicis Research Center Sherman Oaks California Recruiting
FOMAT - Allergy, Asthma & Immunology Medical Group Ventura California Recruiting
Direct Helpers Research Center Hialeah Florida Recruiting
Well Pharma Medical Research, Corp. Miami Florida Recruiting
Deluxe Health Center, LLC Miami Lakes Florida Recruiting
GCP, Global Clinical Professionals St. Petersburg Florida Recruiting
Advanced Clinical Research Institute Tampa Florida Recruiting
Centricity Research Columbus Dermatology Columbus Georgia Recruiting
Treasure Valley Medical Research Boise Idaho Recruiting
Endeavor Health Clinical Trials Center Skokie Illinois Recruiting
Equity Medical, LLC Bowling Green Kentucky Recruiting
Advanced ENT and Allergy, PLLC Louisville Kentucky Recruiting
Johns Hopkins University Baltimore Maryland Recruiting
Revival Research Institute, LLC Troy Michigan Recruiting
Equity Medical, LLC New York New York Recruiting
Markowitz Medical PLLC dba OptiSkin Medical New York New York Recruiting
University of Cincinnati Cincinnati Ohio Not Yet Recruiting
Allergy, Asthma & Clinical Research Center Oklahoma City Oklahoma Recruiting
Advanced Dermatology and Cosmetic Surgery - Spartanburg Spartanburg South Carolina Recruiting
RFSA Dermatology San Antonio Texas Recruiting
Allergy Associates of Utah Sandy City Utah Recruiting
Universitätsklinikum Augsburg, Klinik für Dermatologie und Allergologie Augsburg Germany Recruiting
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP Immunologie und Allergologie IA c/o Charité - Universitätsmedizin Berlin Berlin Germany Recruiting
Elbe Kliniken Buxtehude Dermatologie Buxtehude Germany Recruiting
Rosenpark Research GmbH Darmstadt Germany Recruiting
Universitätsklinikum Carl Gustav Carus Dresden, Klinik und Poliklinik für Dermatologie Dresden Germany Recruiting
Department of Dermatology, University Hospital Dusseldorf Düsseldorf Germany Recruiting
Hautklinik, Uniklinkum Erlangen Erlangen Germany Recruiting
Universitätsklinikum Göttingen -- George-August-Universitat Göttinggen, Klinik für Dermatoogie, Venerologie und Allergologie Göttingen Germany Recruiting
Universitätsklinikum Heidelberg, Klinik für Dermatologie Heidelberg Germany Not Yet Recruiting
MVZ DermaKiel GmbH Kiel Germany Recruiting
Universitätsklinikum Schleswig-Holstein Universität zu Lübeck - Campus Lübeck Lübeck Germany Recruiting
Klinik und Poliklinik für Dermatologie und Allergologie, LMU Klinikum; DASZ-Dermato-Allergologisches Studienzentrum München Germany Recruiting
Universitätsklinikum Münster, Klinik u. Poliklinik f. Dermatologie Münster Germany Recruiting
Universitäts-Hautklinik Tübingen Studienzentrum Immundermatologie Tübingen Germany Recruiting

+ 32 more sites — see the full list on the official registry below.

More Celldex Therapeutics trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07266402 on ClinicalTrials.gov ↗ ← All trials in the UK