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A Study Evaluating the Efficacy and Safety of Momelotinib in Participants With Vacuoles, E1-enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) Syndrome (ATLAS)

29 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Tipo di studio

Interventistico

Iscrizione (Stimato)

136

Fase

  • Fase 2
  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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:

    1. Documented evidence of a canonical, pathogenic Ubiquitin-like modifier activating enzyme 1 (UBA1) mutation
    2. 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:

    1. Is a Participant of non-childbearing potential (PONCBP) OR
    2. 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:

    1. VEXAS-directed therapies (washout period) up to 5 half-lives or up 14 days if half-life is <3 days
    2. 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.
    3. Hematologic support therapy (e.g., ESAs, danazol, luspatercept, G-CSF): 4 weeks
    4. Cell-depleting therapies such as anti-CD20 (rituximab): 12 months
    5. 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:

    1. Unstable angina pectoris
    2. Symptomatic congestive heart failure
    3. Uncontrolled cardiac arrhythmia
    4. QTc >450 msec or QTc >480 msec for participants with bundle branch block.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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
Altri nomi:
  • GSK3070785
Glucocorticoids (prednisone or prednisolone) will be administered
Sperimentale: 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
Altri nomi:
  • GSK3070785
Glucocorticoids (prednisone or prednisolone) will be administered
Comparatore placebo: 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
Verrà somministrato il placebo
Glucocorticoids (prednisone or prednisolone) will be administered

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
ORR (Objective response rate) at Week 26
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Phase 2: Percentage of participants with partial response (PR) or complete response (CR) at Week 26
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: Up to 26 Weeks
Up to 26 Weeks
Number of flare-free days
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Up to Week 108
Up to Week 108
Number of participants with adverse events (AEs) and Serious adverse events (SAEs) by severity
Lasso di tempo: Up to Week 108
Up to Week 108
Number of participants with AEs leading to discontinuation or dose modifications
Lasso di tempo: Up to Week 108
Up to Week 108
Plasma concentration of momelotinib and M21
Lasso di tempo: Up to 26 Weeks
Up to 26 Weeks
Overall Survival
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Direttore dello studio: GSK Clinical Trials, GlaxoSmithKline

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

5 agosto 2026

Completamento primario (Stimato)

6 dicembre 2028

Completamento dello studio (Stimato)

4 giugno 2031

Date di iscrizione allo studio

Primo inviato

28 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 aprile 2026

Primo Inserito (Effettivo)

6 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Sindrome VEXAS

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