- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 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
연구 개요
상세 설명
연구 유형
등록 (추정된)
단계
- 3단계
연락처 및 위치
연구 연락처
- 이름: Novartis Pharmaceuticals
- 전화번호: +41613241111
- 이메일: novartis.email@novartis.com
연구 연락처 백업
- 이름: Novartis Pharmaceuticals
- 전화번호: +81337978748
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Remibrutinib
Participants will receive remibrutinib 25 mg twice a day for 12 weeks.
|
Remibrutinib 25 mg twice a day.
다른 이름들:
|
|
실험적: 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.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Proportion of participants achieving Urticaria Activity Score over 7 days (UAS7) ≤6 (yes/no)
기간: 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
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Proportion of participants achieving UAS7 ≤6 (yes/no)
기간: 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)
기간: 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.
기간: 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
기간: 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)
기간: 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.
기간: 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.
기간: 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
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- CLOU064A2307
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
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
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미국 FDA 규제 기기 제품 연구
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