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

22 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

190

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Cina, 200040
        • Huashan Hospital Affiliated to Fudan University
        • Investigatore principale:
          • Wenyu Wu
        • Contatto:
    • Zhejiang
      • Hangzhou, Zhejiang, Cina, 310006
        • Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University
        • Investigatore principale:
          • Liming Wu
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: HRS-3095 Group
HRS-3095 in different doses.
HRS-3095 tablet.
Comparatore placebo: HRS-3095 placebo Group
HRS-3095 blank preparation.
HRS-3095 tablet placebo.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 4.
Lasso di tempo: Up to 4 weeks.
Up to 4 weeks.

Misure di risultato secondarie

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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 dicembre 2026

Completamento dello studio (Stimato)

1 marzo 2027

Date di iscrizione allo studio

Primo inviato

22 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

22 maggio 2026

Primo Inserito (Effettivo)

29 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

29 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

22 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Orticaria cronica spontanea

Prove cliniche su HRS-3095 Tablet

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