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- Klinische proef NCT07569081
A Study Evaluating the Efficacy and Safety of Momelotinib in Participants With Vacuoles, E1-enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) Syndrome (ATLAS)
29 mei 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
136
Fase
- Fase 2
- Fase 3
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: US GSK Clinical Trials Call Center
- Telefoonnummer: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Studie Contact Back-up
- Naam: EU GSK Clinical Trials Call Center
- Telefoonnummer: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.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:
- 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.
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: 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
Andere namen:
Glucocorticoids (prednisone or prednisolone) will be administered
|
|
Experimenteel: 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
Andere namen:
Glucocorticoids (prednisone or prednisolone) will be administered
|
|
Placebo-vergelijker: 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
|
Placebo zal worden toegediend
Glucocorticoids (prednisone or prednisolone) will be administered
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
ORR (Objective response rate) at Week 26
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Phase 2: Percentage of participants with partial response (PR) or complete response (CR) at Week 26
Tijdsspanne: 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
Tijdsspanne: Up to 26 Weeks
|
Up to 26 Weeks
|
|
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Phase 2: Plasma concentrations of momelotinib and metabolite of momelotinib 21 (M21) to support identification of the RP3D
Tijdsspanne: Up to 26 Weeks
|
Up to 26 Weeks
|
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Number of flare-free days
Tijdsspanne: 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.
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Up to 26 Weeks
|
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Duration of response (DoR)
Tijdsspanne: Up to 104 Weeks
|
DoR defined as the date of clinical response (CR or PR) to the date of relapse.
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Up to 104 Weeks
|
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Number of flare-free days with glucocorticoid (GC) dose <=10 mg/day
Tijdsspanne: 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
|
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Percentage of participants achieving complete and partial biochemical response
Tijdsspanne: Up to 26 Weeks
|
Complete biological response is defined as complete or partial normalization of C-reactive protein.
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Up to 26 Weeks
|
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Objective response rate (ORR) at Week 52
Tijdsspanne: At Week 52
|
ORR is defined as the proportion of participants who have achieved complete response or partial response
|
At Week 52
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Number of Participants with Hematologic Improvement- Erythroid (HI-E) response per International Working Group (IWG) 2018 criteria
Tijdsspanne: 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
|
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Change from Baseline in Short Form 36 (SF-36) domain and summary scores
Tijdsspanne: 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.
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Baseline and up to Week 48
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Change from Baseline in European Organization for Research and Treatment of Cancer Item Library (EORTC IL) 479 score
Tijdsspanne: 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.
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Baseline and up to Week 156
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Change From Baseline in Patient Reported Outcome Measurement Information System (PROMIS) Physical Function Short Form 10b
Tijdsspanne: 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
|
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Change from Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-FATIGUE)
Tijdsspanne: 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
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Changes from Baseline in Patient Global Impression of Severity (PGIS) scores
Tijdsspanne: 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).
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Baseline and up to Week 156
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Changes in Patient Global Impression of Change (PGIC) scores
Tijdsspanne: 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).
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Baseline and up to Week 156
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Changes from Baseline in European quality of life 5 dimensions 5 level version (EQ-5D-5L)
Tijdsspanne: 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.
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Baseline and up to Week 48
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Changes from Baseline in European quality of life-Visual Analogue Scale (EQ-VAS)
Tijdsspanne: 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.
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Baseline and up to Week 48
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Number of participants with adverse events (AEs) and Serious adverse events (SAEs)
Tijdsspanne: Up to Week 108
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Up to Week 108
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|
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Number of participants with adverse events (AEs) and Serious adverse events (SAEs) by severity
Tijdsspanne: Up to Week 108
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Up to Week 108
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Number of participants with AEs leading to discontinuation or dose modifications
Tijdsspanne: Up to Week 108
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Up to Week 108
|
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Plasma concentration of momelotinib and M21
Tijdsspanne: Up to 26 Weeks
|
Up to 26 Weeks
|
|
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Overall Survival
Tijdsspanne: 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
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Studie directeur: GSK Clinical Trials, GlaxoSmithKline
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)
5 augustus 2026
Primaire voltooiing (Geschat)
6 december 2028
Studie voltooiing (Geschat)
4 juni 2031
Studieregistratiedata
Eerst ingediend
28 april 2026
Eerst ingediend dat voldeed aan de QC-criteria
28 april 2026
Eerst geplaatst (Werkelijk)
6 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
1 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
29 mei 2026
Laatst geverifieerd
1 mei 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 223401
- 2025-524416-11-00 (Andere identificatie: EU CT Number)
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Ja
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 .