- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07569081
A Study Evaluating the Efficacy and Safety of Momelotinib in Participants With Vacuoles, E1-enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) Syndrome (ATLAS)
2026년 5월 29일 업데이트: GlaxoSmithKline
A Randomized Phase 2/3, Double-blind, Placebo Controlled Adaptive Study Evaluating the Efficacy and Safety of Momelotinib in Participants With VEXAS Syndrome
This study will assess the efficacy and safety of momelotinib in participants with a diagnosis of VEXAS.
연구 개요
연구 유형
중재적
등록 (추정된)
136
단계
- 2 단계
- 3단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: US GSK Clinical Trials Call Center
- 전화번호: 877-379-3718
- 이메일: GSKClinicalSupportHD@gsk.com
연구 연락처 백업
- 이름: EU GSK Clinical Trials Call Center
- 전화번호: +44 (0) 20 89904466
- 이메일: GSKClinicalSupportHD@gsk.com
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
아니
설명
Inclusion Criteria:
- Age greater than equal to (>=)18 years OR of legal age of consent in the jurisdiction in which the study is taking place, at the time of signing the Informed Consent Form.
Confirmed diagnosis of clinical VEXAS defined by:
- Documented evidence of a canonical, pathogenic Ubiquitin-like modifier activating enzyme 1 (UBA1) mutation
- Inflammatory manifestations: current or documented past involvement within 6 months of at least one organ system
- Receiving glucocorticoid (GC) treatment (prednisone/prednisolone) for >=4 consecutive weeks for >=10 days prior to randomization.
A female participant is eligible to participate if she is not pregnant or breastfeeding and one of the following conditions applies:
- Is a Participant of non-childbearing potential (PONCBP) OR
- Is a Participant of childbearing potential (POCBP) and using a contraceptive method that is highly effective
- Is capable of giving signed informed consent including compliance with the requirements and restrictions
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 to 2 at the time of screening.
- Has adequate organ function
Exclusion Criteria:
- More than 1 prior admission to an intensive care unit due to a VEXAS flare within the 6 months prior to randomization.
- History of severe corticosteroid toxicity: uncontrolled concomitant cardiovascular, nervous system, pulmonary (including obstructive pulmonary disease), renal, hepatic, endocrine (including uncontrolled diabetes mellitus), psychiatric, osteoporosis/osteomalacia, glaucoma, corneal ulcers/injuries, nausea or vomiting or gastrointestinal disease.
- High risk/very high risk Myelodysplastic syndrome (MDS), according to the Revised International Prognostic Scoring System (IPSS-R) with overall risk score >3.5.
- Peripheral blood blast counts >=10%.
- Multiple myeloma (all stages) and other active plasma cell dyscrasias requiring treatment.
- Malignancy (except disease under study including Lower-risk myelodysplastic syndrome [LR-MDS]) that has progressed or required active treatment within the past (24 months) except for basal cell or squamous cell carcinomas of the skin or in-situ carcinomas).
- Uncontrolled intercurrent illness within 12 weeks prior to initiation of momelotinib.
- Ongoing adverse reaction(s) from prior therapy that have not recovered to Grade <=1 per NCI CTCAE v6.0 or to the Baseline status preceding prior therapy
- Psychiatric illness, social situation, or any other condition that would limit informed consent and/or compliance with trial requirements or may interfere with the interpretation of study results, as judged by Investigator or Sponsor.
- Has any clinically significant gastrointestinal conditions or abnormalities that may alter absorption or swallowing
- Known contraindication or hypersensitivity to momelotinib and its metabolites, or any of their excipients.
- Presence of peripheral neuropathy >=Grade 2 per NCI CTCAE v6.0.
- Known history of disseminated mycobacterial infection.
- Known positive status for human immunodeficiency virus (HIV).
- Positive QuantiFERON (or other interferon gamma release assay) during Screening.
- Unable to receive any Pneumocystis jiroveci pneumonia (PJP) medical prophylaxis
- Known clinically significant anemia due to iron, vitamin B12 or folate deficiencies, or autoimmune or hereditary hemolytic anemia, gastrointestinal bleeding, or thalassemia.
- More than 1 prior line of VEXAS directed therapy before or after VEXAS diagnosis or other medical condition.
Use of the following treatments within the noted time periods referenced from date of randomization:
- VEXAS-directed therapies (washout period) up to 5 half-lives or up 14 days if half-life is <3 days
- Other non-GC anti-inflammatory therapies: for non-biologics): 14 days or five half-lives, whichever is longer; for biologics): 28 days or two half-lives whichever is longer.
- Hematologic support therapy (e.g., ESAs, danazol, luspatercept, G-CSF): 4 weeks
- Cell-depleting therapies such as anti-CD20 (rituximab): 12 months
- Investigational agent from a class not otherwise specified: 5 half-lives or 60 days, whichever is longer
- GC use for conditions other than VEXAS, which would interfere with adherence to the fixed GC taper regimen and/or to assessment of efficacy.
- Chronic use of systemic corticosteroids for >4 years or inability to withdraw corticosteroid treatment
- Planned allogeneic HSCT for MDS or VEXAS, within 1 year.
- Any major surgery within 28 days prior to randomization.
- Prior allogeneic/autologous stem cell transplant or solid organ transplant (other than corneal).
- Presence of peripheral neuropathy >=Grade 2 per NCI CTCAE v6.0.
- Hepatitis B or C active infection, unless protocol defined criteria are met.
Any of the following conditions within 6 months prior to randomization:
- Unstable angina pectoris
- Symptomatic congestive heart failure
- Uncontrolled cardiac arrhythmia
- QTc >450 msec or QTc >480 msec for participants with bundle branch block.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Momelotinib Dose level 1 + Glucocorticoids
Participants will receive momelotinib at dose level 1 along with glucocorticoids as a background therapy (prednisone or prednisolone).
Due to adaptive design of the study, additional participants may be randomized to this arm in phase 3.
|
Momelotinib will be administered
다른 이름들:
Glucocorticoids (prednisone or prednisolone) will be administered
|
|
실험적: Momelotinib Dose level 2 + Glucocorticoids
Participants will receive momelotinib at dose level 2 along with glucocorticoids as a background therapy (prednisone or prednisolone).
Due to adaptive design of the study, additional participants may be randomized to this arm in phase 3
|
Momelotinib will be administered
다른 이름들:
Glucocorticoids (prednisone or prednisolone) will be administered
|
|
위약 비교기: Placebo + Glucocorticoids
Participants will receive momelotinib matched placebo along with glucocorticoids as a background therapy(prednisone or prednisolone).
Due to adaptive design of the study, additional participants may be randomized to this arm in phase 3
|
플라시보가 투여될 것이다
Glucocorticoids (prednisone or prednisolone) will be administered
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
ORR (Objective response rate) at Week 26
기간: At Week 26
|
ORR is defined as the proportion of participants who have achieved complete response (CR) or partial response (PR) during the 26-week Primary Treatment Period.
|
At Week 26
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Phase 2: Percentage of participants with partial response (PR) or complete response (CR) at Week 26
기간: At Week 26
|
Percentage of participants with PR or CR at Week 26 to support identification of the Recommended Phase 3 dose (RP3D)
|
At Week 26
|
|
Phase 2: Number of participants with adverse events and clinically significant changes in laboratory parameters, and vital signs to support identification of the RP3D
기간: Up to 26 Weeks
|
Up to 26 Weeks
|
|
|
Phase 2: Plasma concentrations of momelotinib and metabolite of momelotinib 21 (M21) to support identification of the RP3D
기간: Up to 26 Weeks
|
Up to 26 Weeks
|
|
|
Number of flare-free days
기간: Up to 26 Weeks
|
Flare-free days are calendar days without clinical evidence of VEXAS flare and without treatment escalation.
Total number of flare-free days is defined as the cumulative number of consecutive and non-consecutive flare-free days.
|
Up to 26 Weeks
|
|
Duration of response (DoR)
기간: Up to 104 Weeks
|
DoR defined as the date of clinical response (CR or PR) to the date of relapse.
|
Up to 104 Weeks
|
|
Number of flare-free days with glucocorticoid (GC) dose <=10 mg/day
기간: Up to 104 Weeks
|
Flare-free days are calendar days without clinical evidence of VEXAS flare and without treatment escalation.
Total number of flare-free days is defined as the cumulative number of consecutive and non-consecutive flare-free days.
|
Up to 104 Weeks
|
|
Percentage of participants achieving complete and partial biochemical response
기간: Up to 26 Weeks
|
Complete biological response is defined as complete or partial normalization of C-reactive protein.
|
Up to 26 Weeks
|
|
Objective response rate (ORR) at Week 52
기간: At Week 52
|
ORR is defined as the proportion of participants who have achieved complete response or partial response
|
At Week 52
|
|
Number of Participants with Hematologic Improvement- Erythroid (HI-E) response per International Working Group (IWG) 2018 criteria
기간: Up to 26 Weeks
|
HI-E response is measured based on the combined incidence of: Low transfusion burden participants defined as absence of any transfusion for greater than or equal to (>=)8 consecutive weeks.
High transfusion burden participants: minor response defined as reduction by >=50% of red blood cell (RBC) units for >=8 consecutive weeks.
Major response defined as absence of RBC transfusions for >=8 consecutive weeks or longer up to 26 weeks.
|
Up to 26 Weeks
|
|
Change from Baseline in Short Form 36 (SF-36) domain and summary scores
기간: Baseline and up to Week 48
|
Short-Form 36 is a health-related survey that assesses quality of life covering 8 domains: vitality; physical functioning; bodily pain; general health perceptions; physical role functioning; emotional role functioning; social role functioning; and mental health.
The domain scores are weighted to a scale ranging between 0 to 100, where higher score represents better health.
The Physical Component Summary (PCS) and Mental Component Summary (MCS) scores are derived from the eight domain scores.
These scores are standardized to a general U.S. population average of 50, with a standard deviation of 10.
For both PCS and MCS, scores range from 0 to 100, higher scores indicate a better health outcome.
|
Baseline and up to Week 48
|
|
Change from Baseline in European Organization for Research and Treatment of Cancer Item Library (EORTC IL) 479 score
기간: Baseline and up to Week 156
|
The EORTC Item Library is a database containing >1000 individual items from more than 70 EORTC quality of life measures.
A subset of 7 items from the library were selected based on symptoms experienced by participants with VEXAS syndrome.
Scores range from 1 to 100 with higher scores representing a higher ("worse") level of symptoms.
|
Baseline and up to Week 156
|
|
Change From Baseline in Patient Reported Outcome Measurement Information System (PROMIS) Physical Function Short Form 10b
기간: Baseline and up to Week 156
|
PROMIS Physical Function Short Form 10b consists of 10 questions; each with a 5-point response.
PROMIS short form assesses self-reported capability of a participant rather than actual performance of physical activities.
Higher scores indicate better functioning.
Total possible range of scores is 10 to 50, with higher scores corresponding to a greater physical function ability.
|
Baseline and up to Week 156
|
|
Change from Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-FATIGUE)
기간: Baseline and up to Week 156
|
The FACIT-Fatigue is a short, 13-item questionnaire that assesses self-reported fatigue and its associated impact on daily activities over the past 7 days.
A higher score indicates a better outcome (no fatigue).
The total score ranges from 0 to 52, with 0 being the worst possible score and 52 being the best possible score (indicating no fatigue).
|
Baseline and up to Week 156
|
|
Changes from Baseline in Patient Global Impression of Severity (PGIS) scores
기간: Baseline and up to Week 156
|
The PGIS is a single global question which asks participants to rate the severity of their VEXAS syndrome symptoms on a 5-point rating scale with response categories of "No symptoms", "Mild", "Moderate", "Severe", and "Very Severe."
The PGIS scores ranges from 0 (absent) to 4 (very severe).
|
Baseline and up to Week 156
|
|
Changes in Patient Global Impression of Change (PGIC) scores
기간: Baseline and up to Week 156
|
The PGIC is a single global question which asks participants to rate the change in severity of their VEXAS syndrome symptoms since starting study medication using a 5-point rating scale with response categories of "much better", "a little better", "no change", "a little worse", "much worse".
The PGIC score ranges from +2 (much better) to -2 (much worse).
|
Baseline and up to Week 156
|
|
Changes from Baseline in European quality of life 5 dimensions 5 level version (EQ-5D-5L)
기간: Baseline and up to Week 48
|
EQ-5D-5L is self-assessment questionnaire, consisting of 5 items covering 5 dimensions (mobility, self care, usual activities, pain/discomfort, and anxiety/depression).
Each dimension is measured by 5-point Likert scale ranging from 1=no problems to 5=extreme problems.
|
Baseline and up to Week 48
|
|
Changes from Baseline in European quality of life-Visual Analogue Scale (EQ-VAS)
기간: Baseline and up to Week 48
|
The EQ-VAS records the respondents self-rated health on a vertical VAS, ranging from 0 to 100, where 0 represents the worst imaginable health and 100 represents the best imaginable health.
|
Baseline and up to Week 48
|
|
Number of participants with adverse events (AEs) and Serious adverse events (SAEs)
기간: Up to Week 108
|
Up to Week 108
|
|
|
Number of participants with adverse events (AEs) and Serious adverse events (SAEs) by severity
기간: Up to Week 108
|
Up to Week 108
|
|
|
Number of participants with AEs leading to discontinuation or dose modifications
기간: Up to Week 108
|
Up to Week 108
|
|
|
Plasma concentration of momelotinib and M21
기간: Up to 26 Weeks
|
Up to 26 Weeks
|
|
|
Overall Survival
기간: At Months 12, 24 and 36
|
Overall survival is defined as the time from randomization to the date of death due to any cause.
|
At Months 12, 24 and 36
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
스폰서
수사관
- 연구 책임자: GSK Clinical Trials, GlaxoSmithKline
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (추정된)
2026년 8월 5일
기본 완료 (추정된)
2028년 12월 6일
연구 완료 (추정된)
2031년 6월 4일
연구 등록 날짜
최초 제출
2026년 4월 28일
QC 기준을 충족하는 최초 제출
2026년 4월 28일
처음 게시됨 (실제)
2026년 5월 6일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 6월 1일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 5월 29일
마지막으로 확인됨
2026년 5월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 223401
- 2025-524416-11-00 (기타 식별자: EU CT Number)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
아니요
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
예
미국 FDA 규제 기기 제품 연구
아니
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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