- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne 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
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 3
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Novartis Pharmaceuticals
- Numer telefonu: +41613241111
- E-mail: novartis.email@novartis.com
Kopia zapasowa kontaktu do badania
- Nazwa: Novartis Pharmaceuticals
- Numer telefonu: +81337978748
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
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.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nielosowe
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Remibrutinib
Participants will receive remibrutinib 25 mg twice a day for 12 weeks.
|
Remibrutinib 25 mg twice a day.
Inne nazwy:
|
|
Eksperymentalny: 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.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Proportion of participants achieving Urticaria Activity Score over 7 days (UAS7) ≤6 (yes/no)
Ramy czasowe: 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
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Proportion of participants achieving UAS7 ≤6 (yes/no)
Ramy czasowe: 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)
Ramy czasowe: 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.
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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.
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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.
Ramy czasowe: 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.
Ramy czasowe: 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
|
Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Procesy patologiczne
- Przewlekła choroba
- Atrybuty choroby
- Choroby układu odpornościowego
- Nadwrażliwość, natychmiastowa
- Nadwrażliwość
- Choroby skórne
- Pokrzywka
- Choroby skóry, naczyniowe
- Stany patologiczne, oznaki i objawy
- Choroby skóry i tkanki łącznej
- Przewlekła pokrzywka
- Aminokwasy, peptydy i białka
- Białka
- Przeciwciała, monoklonalne, humanizowane
- Przeciwciała, monoklonalne
- Przeciwciała
- Immunoglobuliny
- Immunoproteiny
- Białka krwi
- Globuliny w surowicy
- Globuliny
- Przeciwciała, antyidiotypowe
- Omalizumab
- remibrutynib
Inne numery identyfikacyjne badania
- CLOU064A2307
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
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
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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