- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07816328
Investigation of a Remibrutinib- and Omalizumab-based Treatment Algorithm in Adult Patients With Chronic Spontaneous Urticaria Inadequately Controlled by H1-antihistamines Within 24 Weeks
A Global, Multi-center, Open-label Study, Investigating a Remibrutinib- and Omalizumab-Based Treatment Algorithm in Adult Patients With Chronic Spontaneous Urticaria Inadequately Controlled by H1-Antihistamines, to Achieve Fast and Well-Controlled Disease Within 24 Weeks
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 3
Kontakter og lokationer
Studiekontakt
- Navn: Novartis Pharmaceuticals
- Telefonnummer: +41613241111
- E-mail: novartis.email@novartis.com
Undersøgelse Kontakt Backup
- Navn: Novartis Pharmaceuticals
- Telefonnummer: +81337978748
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Key Inclusion Criteria:
- Male and female adults (age ≥18 years) at the time of signing the informed consent.
- CSU duration for ≥2 months prior to screening (defined as the onset of CSU determined by the Investigator based on all available supporting documentation).
Diagnosis of CSU inadequately controlled by sgH1-AH at baseline defined as:
- The presence of itch and hives for ≥6 consecutive weeks prior to screening despite the use of sgH1-AH during this time period.
- UAS7 score (range: 0-42) ≥16.
- Documentation of hives within two months prior to baseline (either at screening and/or at baseline; or documented in the participant's medical history).
- Willing and able to complete an Urticaria Patient Daily Diary (UPDD) for the duration of the study and adhere to the study protocol.
- Participants must not have had more than one missing UPDD entry (either morning or evening) in the 7 days prior to enrollment (Day 1).
Key Exclusion Criteria:
- Previous use of remibrutinib, other Bruton's tyrosine kinase (BTK) inhibitors or prior exposure to biologics with any effect in CSU (e.g., ligelizumab, omalizumab, dupilumab, barzolvolimab).
- Evidence of clinically significant cardiovascular (such as but not limited to myocardial infarction, unstable ischemic heart disease, New York Heart Association (NYHA) Class III/IV left ventricular failure, arrhythmia and uncontrolled hypertension within 12 months prior to Visit 1), neurological, psychiatric, pulmonary, renal, hepatic, endocrine, metabolic, gastrointestinal, or hematological disorders, or immunodeficiency that, in the investigator's opinion, would compromise the safety of the participant, interfere with the interpretation of the study results or otherwise preclude participation or protocol adherence by the participant.
- Significant bleeding risk or coagulation disorders.
- History of gastrointestinal bleeding, e.g., in association with use of nonsteroidal anti-inflammatory drugs (NSAIDs), that was clinically relevant (e.g., where intervention was indicated or requiring hospitalization or blood transfusion).
- Requirement for anti-platelet medication, except for acetylsalicylic acid up to 100 mg/d or clopidogrel up to 75mg/d. The use of dual anti-platelet therapy (e.g., acetylsalicylic acid + clopidogrel) is prohibited.
- Requirement for anticoagulant medication (for example, warfarin or Novel Oral Anti- Coagulant - NOAC).
- History or current hepatic disease including but not limited to acute or chronic hepatitis, cirrhosis or hepatic failure or aspartate aminotransferase (AST) / alanine aminotransferase (ALT) levels of more than 1.5x upper limit of normal (ULN) or international normalized ratio (INR) of more than 1.5 at screening.
Other protocol-defined inclusion/exclusion criteria may apply.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Remibrutinib
Participants will receive remibrutinib 25 mg twice a day for 12 weeks.
|
Remibrutinib 25 mg twice a day.
Andre navne:
|
|
Eksperimentel: Remibrutinib or Omalizumab
Participants will receive remibrutinib 25 mg twice a day.
At Week 12, well-controlled participants (UCT7 ≥12) continue remibrutinib, while participants with inadequate control (UCT7 <12) escalate to omalizumab 300 mg every 4 weeks.
|
Omalizumab 300 mg every 4 weeks.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Proportion of participants achieving Urticaria Activity Score over 7 days (UAS7) ≤6 (yes/no)
Tidsramme: Week 24
|
UAS7 is a validated patient-reported measure of chronic spontaneous urticaria disease activity over 7 days.
It is calculated as the sum of the weekly Hives Severity Score (HSS7) and the weekly Itch Severity Score (ISS7) and ranges from 0 to 42.
Lower scores indicate lower disease activity / better disease control, and a score of ≤6 indicates well-controlled disease.
HSS7 and ISS7 are each derived from daily diary entries over the 7 days preceding the visit.
|
Week 24
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Proportion of participants achieving UAS7 ≤6 (yes/no)
Tidsramme: Weeks 16 and 20
|
UAS7 is calculated as the sum of the HSS7 and ISS7 and ranges from 0 to 42.
Lower scores indicate lower disease activity / better disease control, and a score of ≤6 indicates well-controlled disease.
HSS7 and ISS7 are each derived from daily diary entries over the 7 days preceding the visit.
|
Weeks 16 and 20
|
|
Proportion of participants achieving UAS7 =0 (yes/no)
Tidsramme: Weeks 16, 20, and 24
|
UAS7 is calculated as the sum of the HSS7 and ISS7 and ranges from 0 to 42, with 0 indicating no urticaria activity over the 7-day assessment period and higher scores indicating worse disease activity.
|
Weeks 16, 20, and 24
|
|
Proportion of participants achieving Angioedema Activity Score over 7 days (AAS7) =0.
Tidsramme: Weeks 16, 20, and 24
|
AAS7 is a validated tool assessing angioedema activity, recorded once daily in the evening in the eDiary.
If no angioedema is reported on a given day, the daily score is 0. Weekly AAS7 scores range from 0 to 105, with higher scores indicating greater angioedema severity; therefore, 0 represents absence of angioedema.
|
Weeks 16, 20, and 24
|
|
Proportion of participants achieving of Dermatology Life Quality Index (DLQI) =0/1
Tidsramme: Weeks 16, 20, and 24
|
DLQI is a 10-item dermatology-specific quality-of-life instrument assessing the impact of skin disease over the previous 7 days.
The total score ranges from 0 to 30, with higher scores indicating worse disease-related quality of life.
A score of 0-1 corresponds to no effect on the participant's life.
|
Weeks 16, 20, and 24
|
|
Incidence and severity of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
Tidsramme: From Day 1 until at least 4 weeks after the last administration of remibrutinib and at least 16 weeks after the last administration of omalizumab
|
To evaluate the safety and tolerability of LOU064.
|
From Day 1 until at least 4 weeks after the last administration of remibrutinib and at least 16 weeks after the last administration of omalizumab
|
|
Proportion of participants achieving UAS7 ≤6 under the treatment algorithm compared with historical omalizumab (300 mg every 4 weeks) data.
Tidsramme: Weeks 16, 20, and 24
|
UAS7 is calculated as the sum of the HSS7 and ISS7 and ranges from 0 to 42.
Lower scores indicate lower disease activity / better disease control, and a score of ≤6 indicates well-controlled disease.
HSS7 and ISS7 are each derived from daily diary entries over the 7 days preceding the visit.
|
Weeks 16, 20, and 24
|
|
Proportion of participants achieving UAS7 =0 under the treatment algorithm compared with historical omalizumab (300 mg every 4 weeks) data.
Tidsramme: Weeks 16, 20, and 24
|
UAS7 is calculated as the sum of the HSS7 and ISS7 and ranges from 0 to 42, with 0 indicating no urticaria activity over the 7-day assessment period and higher scores indicating worse disease activity.
|
Weeks 16, 20, and 24
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Patologiske processer
- Kronisk sygdom
- Sygdomsegenskaber
- Sygdomme i immunsystemet
- Overfølsomhed, Øjeblikkelig
- Overfølsomhed
- Hudsygdomme
- Nældefeber
- Hudsygdomme, vaskulære
- Patologiske tilstande, tegn og symptomer
- Hud- og bindevævssygdomme
- Kronisk nældefeber
- Aminosyrer, peptider og proteiner
- Proteiner
- Antistoffer, monoklonal, humaniseret
- Antistoffer, monoklonal
- Antistoffer
- Immunoglobuliner
- Immunoproteiner
- Blodproteiner
- Serum globuliner
- Globuliner
- Antistoffer, anti-idiotypisk
- Omalizumab
- Remibrutinib
Andre undersøgelses-id-numre
- CLOU064A2307
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Novartis is committed to sharing access to patient-level data and supporting clinical documents from eligible studies with qualified external researchers. Requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to protect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .