- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07613866
A Clinical Trial of HRS-3095 in Patients With Chronic Spontaneous Urticaria
22 mai 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
190
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Yijia Xu
- Numéro de téléphone: +86-0518-81220121
- E-mail: yijia.xu@hengrui.com
Lieux d'étude
-
-
Shanghai Municipality
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Shanghai, Shanghai Municipality, Chine, 200040
- Huashan Hospital Affiliated to Fudan University
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Chercheur principal:
- Wenyu Wu
-
Contact:
- Wenyu Wu
- Numéro de téléphone: +86-021-52887783
- E-mail: 13601983907@139.com
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-
Zhejiang
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Hangzhou, Zhejiang, Chine, 310006
- Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University
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Chercheur principal:
- Liming Wu
-
Contact:
- Liming Wu
- Numéro de téléphone: +86-13750837205
- E-mail: 18957118053@163.com
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-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Inclusion Criteria:
- 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.
- Participants must have a history of chronic spontaneous urticaria (CSU) with a disease duration of at least 6 months prior to screening.
- 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.
- At randomization, the UAS7 score must be ≥16 (range: 0-42) and the HSS7 score ≥ 8 (range: 0-21).
- 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.
- 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.
- 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.
- 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:
- Any skin disease that could interfere with study assessment (e.g., chronic inducible urticaria, urticarial vasculitis, atopic dermatitis, psoriasis).
- Use of systemic or topical medications with therapeutic or immunomodulatory effects on the study disease during the relevant washout period prior to screening.
- 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.
- 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.
- 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).
- History of liver disease or current treatment for liver disease (e.g., hepatitis, cirrhosis, liver failure).
- History of systemic antimicrobial use or presence of superficial skin infection (e.g., impetigo) within 4 weeks prior to screening.
- History of malignancy or current malignancy (excluding completely resected and recurrence-free basal cell carcinoma, squamous cell carcinoma, or cervical intraepithelial neoplasia).
- Major surgery performed within 3 months prior to randomization or planned during the study.
- Serious concomitant disease or any condition judged by the investigator to make the participant unsuitable for study participation.
- 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.
- Pregnant or breastfeeding women.
- Allergy to the study drug or any of its components.
- 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.
- 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 d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: HRS-3095 Group
HRS-3095 in different doses.
|
HRS-3095 tablet.
|
|
Comparateur placebo: HRS-3095 placebo Group
HRS-3095 blank preparation.
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HRS-3095 tablet placebo.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 4.
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
The concentration of HRS-3095 in serum (Cmax)
Délai: 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
Délai: 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)
Délai: 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
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Percentage change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 2 and 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Percentage change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Percentage change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Proportion of patients with UAS7 ≤ 6 at Week 2 and 4 compared to baseline
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Proportion of patients with UAS7 = 0 at Week 2 and 4 compared to baseline
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Proportion of patients achieving the Minimum Important Difference (MID) in UAS7 at Week 2 and 4
Délai: Up to 4 weeks.
|
≥ 10-point decrease from baseline.
|
Up to 4 weeks.
|
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Proportion of patients achieving the Minimum Important Difference (MID) in ISS7 at Week 2 and 4
Délai: Up to 4 weeks.
|
≥ 5-point decrease from baseline.
|
Up to 4 weeks.
|
|
Time to achieve the Minimum Important Difference (MID) in UAS7
Délai: Up to 4 weeks.
|
≥ 10-point decrease from baseline.
|
Up to 4 weeks.
|
|
Time to achieve the Minimum Important Difference (MID) in ISS7
Délai: 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
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Urticaria Control Test (UCT) from baseline at Week 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Proportion of participants with UCT ≥ 12 at Week 4 compared to baseline
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Dermatology Life Quality Index (DLQI) from baseline at Week 4
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Proportion of participants with DLQI = 0 or 1 at Week 4 compared to baseline
Délai: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Adverse events
Délai: From the beginning of administration to the 8th week.
|
From the beginning of administration to the 8th week.
|
|
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Plasma concentrations of HRS-3095 and its metabolites
Délai: 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)
Délai: From the beginning of administration to the 4th week.
|
From the beginning of administration to the 4th week.
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 juillet 2026
Achèvement primaire (Estimé)
1 décembre 2026
Achèvement de l'étude (Estimé)
1 mars 2027
Dates d'inscription aux études
Première soumission
22 mai 2026
Première soumission répondant aux critères de contrôle qualité
22 mai 2026
Première publication (Réel)
29 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
29 mai 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
22 mai 2026
Dernière vérification
1 mai 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Processus pathologiques
- Maladie chronique
- Attributs de la maladie
- Maladies du système immunitaire
- Hypersensibilité immédiate
- Hypersensibilité
- Maladies de la peau
- Urticaire
- Maladies de la peau, vasculaire
- Conditions pathologiques, signes et symptômes
- Maladies de la peau et du tissu conjonctif
- Urticaire chronique
Autres numéros d'identification d'étude
- HRS-3095-201
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
INDÉCIS
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .