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Clinical trial to evaluate the efficacy and safety of CDX-0159 in patients with chronic inducible urticaria.

THE PURPOSE OF THE STUDY IS TO EVALUATE THE SAFETY OF CDX-0159, THE STUDY DRUG, IN SUBCUTANEOUS (SC) INJECTION, UNDER THE SKIN, AND TO TEST ITS EFFECTS IN PEOPLE, AS WELL AS TO EVALUATE THE EFFICACY OF DIFFERENT CDX-0159 REGIMENS.

En la imagen se puede observar a la Dra. Marta Ferrer Puga, una destacada especialista en Alergología en la Clínica Universidad de Navarra. La Dra. Ferrer cuenta con una amplia experiencia en el diagnóstico y tratamiento de la urticaria crónica y angioedema, ofreciendo soluciones personalizadas y efectivas a sus pacientes.En la Clínica Universidad de Navarra, contamos con un equipo multidisciplinar de profesionales altamente capacitados y tecnología avanzada para brindar atención médica excepcional a nuestros pacientes. Nos enfocamos en proporcionar un servicio personalizado y de alta calidad a quienes confían en nosotros para el manejo de su salud.Si necesita más información sobre nuestros servicios de Alergología, no dude en contactarnos.
Dr. Marta Ferrer Puga Curriculum
Specialist Allergy and Immunology Department
Navarre headquarters
Madrid headquarters
Status
In recruitment
headquarters
Pamplona

Technical Summary

  • PHASE II DOSE-FINDING, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSE-FINDING STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CDX-0159 IN PATIENTS WITH CHRONIC INDUCIBLE URTICARIA
  • Code EudraCT: 2021-006447-95
  • Protocol number: CDX0159-07
  • Promoter: Celldex Therapeutics
  • Link to Clinical Trials

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

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