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A Clinical Trial of HRS-3095 in Patients With Chronic Spontaneous Urticaria

22 de mayo de 2026 actualizado por: Chengdu Suncadia Medicine Co., Ltd.

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase II Clinical Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of HRS-3095 in Patients With Chronic Spontaneous Urticaria

The study is being conducted to evaluate the efficacy, and safety of HRS-3095 with Chronic Spontaneous in adults, and to explore the reasonable dosage of HRS-3095 for Chronic Spontaneous Urticaria.

Descripción general del estudio

Estado

Aún no reclutando

Tipo de estudio

Intervencionista

Inscripción (Estimado)

190

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Yijia Xu
  • Número de teléfono: +86-0518-81220121
  • Correo electrónico: yijia.xu@hengrui.com

Ubicaciones de estudio

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Porcelana, 200040
        • Huashan Hospital Affiliated to Fudan University
        • Investigador principal:
          • Wenyu Wu
        • Contacto:
    • Zhejiang
      • Hangzhou, Zhejiang, Porcelana, 310006
        • Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University
        • Investigador principal:
          • Liming Wu
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Participants must be between 18 and 70 years of age, inclusive, at the time of signing the Informed Consent Form (ICF), with no restriction on gender.
  2. Participants must have a history of chronic spontaneous urticaria (CSU) with a disease duration of at least 6 months prior to screening.
  3. Participants must be diagnosed with H1-antihistamine-inadequately-controlled CSU at screening, defined as: having had persistent symptoms of pruritus and wheals for ≥6 weeks prior to screening, despite regular use of second-generation H1-antihistamines during that period.
  4. At randomization, the UAS7 score must be ≥16 (range: 0-42) and the HSS7 score ≥ 8 (range: 0-21).
  5. Participants must have been on a stable dose of the specified second-generation H1-antihistamine for at least 3 days prior to the first UAS score at screening.
  6. Participants must be willing and able to complete logbook entries as required during the study and must have no missing daily UAS scores during the 7 days before randomization.
  7. Participants must voluntarily sign the Informed Consent Form (ICF) before any study-related procedures, be able to communicate effectively with the investigator, and be willing to strictly adhere to the requirements of the study protocol.
  8. Female participants of childbearing potential or male participants with a female partner of childbearing potential must agree to avoid donating sperm or ova and must agree to take highly effective contraceptive measures from the time of signing the ICF until 3 months after the last dose.

Exclusion Criteria:

  1. Any skin disease that could interfere with study assessment (e.g., chronic inducible urticaria, urticarial vasculitis, atopic dermatitis, psoriasis).
  2. Use of systemic or topical medications with therapeutic or immunomodulatory effects on the study disease during the relevant washout period prior to screening.
  3. Use of investigational drugs or medical devices within 8 weeks or 5 half-lives (if known), whichever is longer, or within 30 days (for small molecules) prior to screening.
  4. Vaccination or exposure to live or attenuated vaccines within 3 months prior to screening or participation in a vaccine-related clinical trial within 3 months prior to randomization.
  5. History or current coagulation-related risk (e.g., bleeding diathesis, coagulopathy, GI bleeding with clinical significance, antiplatelet or anticoagulant use, history of thrombosis or thromboembolic events, or increased risk of thrombosis).
  6. History of liver disease or current treatment for liver disease (e.g., hepatitis, cirrhosis, liver failure).
  7. History of systemic antimicrobial use or presence of superficial skin infection (e.g., impetigo) within 4 weeks prior to screening.
  8. History of malignancy or current malignancy (excluding completely resected and recurrence-free basal cell carcinoma, squamous cell carcinoma, or cervical intraepithelial neoplasia).
  9. Major surgery performed within 3 months prior to randomization or planned during the study.
  10. Serious concomitant disease or any condition judged by the investigator to make the participant unsuitable for study participation.
  11. Abnormal findings in vital signs, physical examination, laboratory tests, ECG, chest X-ray/CT, or abdominal ultrasound during screening that have clinical significance and may affect study validity or participant safety.
  12. Pregnant or breastfeeding women.
  13. Allergy to the study drug or any of its components.
  14. History of alcohol abuse within 6 months prior to screening (e.g., > 14 units/week) or history of illicit drug abuse within 6 months prior to screening.
  15. Any condition judged by the investigator that may affect the safety or efficacy evaluation of the study drug or participant compliance with the study procedures or diary.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: HRS-3095 Group
HRS-3095 in different doses.
HRS-3095 tablet.
Comparador de placebos: HRS-3095 placebo Group
HRS-3095 blank preparation.
HRS-3095 tablet placebo.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 4.
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The concentration of HRS-3095 in serum (Cmax)
Periodo de tiempo: From the beginning of administration to the 4th week.
From the beginning of administration to the 4th week.
The time of metabolism of the drug in the serum
Periodo de tiempo: From the beginning of administration to the 4th week.
The concentration of HRS-3095 in plasma will be determined.
From the beginning of administration to the 4th week.
The concentration of HRS-3095 in serum (AUC)
Periodo de tiempo: From the beginning of administration to the 4th week.
The concentration of HRS-3095 in plasma will be determined.
From the beginning of administration to the 4th week.
Change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 2
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Percentage change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Percentage change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Percentage change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Proportion of patients with UAS7 ≤ 6 at Week 2 and 4 compared to baseline
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Proportion of patients with UAS7 = 0 at Week 2 and 4 compared to baseline
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Proportion of patients achieving the Minimum Important Difference (MID) in UAS7 at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
≥ 10-point decrease from baseline.
Up to 4 weeks.
Proportion of patients achieving the Minimum Important Difference (MID) in ISS7 at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
≥ 5-point decrease from baseline.
Up to 4 weeks.
Time to achieve the Minimum Important Difference (MID) in UAS7
Periodo de tiempo: Up to 4 weeks.
≥ 10-point decrease from baseline.
Up to 4 weeks.
Time to achieve the Minimum Important Difference (MID) in ISS7
Periodo de tiempo: Up to 4 weeks.
≥ 10-point decrease from baseline.
Up to 4 weeks.
Change in 7-day Angioedema Activity Score (AAS7) from baseline at Week 2 and 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Change in Urticaria Control Test (UCT) from baseline at Week 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Proportion of participants with UCT ≥ 12 at Week 4 compared to baseline
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Change in Dermatology Life Quality Index (DLQI) from baseline at Week 4
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Proportion of participants with DLQI = 0 or 1 at Week 4 compared to baseline
Periodo de tiempo: Up to 4 weeks.
Up to 4 weeks.
Adverse events
Periodo de tiempo: From the beginning of administration to the 8th week.
From the beginning of administration to the 8th week.
Plasma concentrations of HRS-3095 and its metabolites
Periodo de tiempo: From the beginning of administration to the 4th week.
From the beginning of administration to the 4th week.
Relative change from baseline in serum total immunoglobulin E (IgE)
Periodo de tiempo: From the beginning of administration to the 4th week.
From the beginning of administration to the 4th week.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de julio de 2026

Finalización primaria (Estimado)

1 de diciembre de 2026

Finalización del estudio (Estimado)

1 de marzo de 2027

Fechas de registro del estudio

Enviado por primera vez

22 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

22 de mayo de 2026

Publicado por primera vez (Actual)

29 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

29 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

22 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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