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- Klinische proef NCT07613866
A Clinical Trial of HRS-3095 in Patients With Chronic Spontaneous Urticaria
22 mei 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
190
Fase
- Fase 2
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Yijia Xu
- Telefoonnummer: +86-0518-81220121
- E-mail: yijia.xu@hengrui.com
Studie Locaties
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, China, 200040
- Huashan Hospital Affiliated to Fudan University
-
Hoofdonderzoeker:
- Wenyu Wu
-
Contact:
- Wenyu Wu
- Telefoonnummer: +86-021-52887783
- E-mail: 13601983907@139.com
-
-
Zhejiang
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Hangzhou, Zhejiang, China, 310006
- Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University
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Hoofdonderzoeker:
- Liming Wu
-
Contact:
- Liming Wu
- Telefoonnummer: +86-13750837205
- E-mail: 18957118053@163.com
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: HRS-3095 Group
HRS-3095 in different doses.
|
HRS-3095 tablet.
|
|
Placebo-vergelijker: HRS-3095 placebo Group
HRS-3095 blank preparation.
|
HRS-3095 tablet placebo.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 4.
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
The concentration of HRS-3095 in serum (Cmax)
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Percentage change in Weekly Urticaria Activity Score (UAS7) from baseline at Week 2 and 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Percentage change in Weekly Itch Severity Score (ISS7) from baseline at Week 2 and 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
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Percentage change in Weekly Wheal Severity Score (HSS7) from baseline at Week 2 and 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Proportion of patients with UAS7 ≤ 6 at Week 2 and 4 compared to baseline
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Proportion of patients with UAS7 = 0 at Week 2 and 4 compared to baseline
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Proportion of patients achieving the Minimum Important Difference (MID) in UAS7 at Week 2 and 4
Tijdsspanne: 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
Tijdsspanne: Up to 4 weeks.
|
≥ 5-point decrease from baseline.
|
Up to 4 weeks.
|
|
Time to achieve the Minimum Important Difference (MID) in UAS7
Tijdsspanne: Up to 4 weeks.
|
≥ 10-point decrease from baseline.
|
Up to 4 weeks.
|
|
Time to achieve the Minimum Important Difference (MID) in ISS7
Tijdsspanne: 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
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Urticaria Control Test (UCT) from baseline at Week 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Proportion of participants with UCT ≥ 12 at Week 4 compared to baseline
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Change in Dermatology Life Quality Index (DLQI) from baseline at Week 4
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Proportion of participants with DLQI = 0 or 1 at Week 4 compared to baseline
Tijdsspanne: Up to 4 weeks.
|
Up to 4 weeks.
|
|
|
Adverse events
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: From the beginning of administration to the 4th week.
|
From the beginning of administration to the 4th week.
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
1 juli 2026
Primaire voltooiing (Geschat)
1 december 2026
Studie voltooiing (Geschat)
1 maart 2027
Studieregistratiedata
Eerst ingediend
22 mei 2026
Eerst ingediend dat voldeed aan de QC-criteria
22 mei 2026
Eerst geplaatst (Werkelijk)
29 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
29 mei 2026
Laatste update ingediend die voldeed aan QC-criteria
22 mei 2026
Laatst geverifieerd
1 mei 2026
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- HRS-3095-201
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
ONBESLIST
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .