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

22 de maio de 2026 atualizado 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.

Visão geral do estudo

Status

Ainda não está recrutando

Tipo de estudo

Intervencional

Inscrição (Estimado)

190

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Quadruplicar

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: HRS-3095 Group
HRS-3095 in different doses.
HRS-3095 tablet.
Comparador de Placebo: HRS-3095 placebo Group
HRS-3095 blank preparation.
HRS-3095 tablet placebo.

O que o estudo está medindo?

Medidas de resultados primários

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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
The concentration of HRS-3095 in serum (Cmax)
Prazo: 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
Prazo: 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)
Prazo: 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
Prazo: Up to 4 weeks.
Up to 4 weeks.
Change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Percentage change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 2 and 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Percentage change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Percentage change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Proportion of patients with UAS7 ≤ 6 at Week 2 and 4 compared to baseline
Prazo: Up to 4 weeks.
Up to 4 weeks.
Proportion of patients with UAS7 = 0 at Week 2 and 4 compared to baseline
Prazo: Up to 4 weeks.
Up to 4 weeks.
Proportion of patients achieving the Minimum Important Difference (MID) in UAS7 at Week 2 and 4
Prazo: 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
Prazo: Up to 4 weeks.
≥ 5-point decrease from baseline.
Up to 4 weeks.
Time to achieve the Minimum Important Difference (MID) in UAS7
Prazo: Up to 4 weeks.
≥ 10-point decrease from baseline.
Up to 4 weeks.
Time to achieve the Minimum Important Difference (MID) in ISS7
Prazo: 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
Prazo: Up to 4 weeks.
Up to 4 weeks.
Change in Urticaria Control Test (UCT) from baseline at Week 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Proportion of participants with UCT ≥ 12 at Week 4 compared to baseline
Prazo: Up to 4 weeks.
Up to 4 weeks.
Change in Dermatology Life Quality Index (DLQI) from baseline at Week 4
Prazo: Up to 4 weeks.
Up to 4 weeks.
Proportion of participants with DLQI = 0 or 1 at Week 4 compared to baseline
Prazo: Up to 4 weeks.
Up to 4 weeks.
Adverse events
Prazo: 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
Prazo: 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)
Prazo: From the beginning of administration to the 4th week.
From the beginning of administration to the 4th week.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de julho de 2026

Conclusão Primária (Estimado)

1 de dezembro de 2026

Conclusão do estudo (Estimado)

1 de março de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

22 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

22 de maio de 2026

Primeira postagem (Real)

29 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

22 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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