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NgFUS NIVO: NeuroNavigation-Guided Focused Ultrasound With Nivolumab in Relapsed and Progressive DMG and Other High Grade Brain Tumors

8 settembre 2026 aggiornato da: Children's National Research Institute

A Safety and Feasibility Study of NeuroNavigation-Guided Low Intensity Focused Ultrasound With Microbubbles to Enhance Nivolumab Delivery for the Treatment of Relapsed and Progressive Diffuse Midline Glioma and Other High Grade Brain Tumors

This is an open-label phase 1 safety and feasibility study evaluating a novel combination therapy for progressive and relapsed diffuse midline glioma (DMG) and other progressive and relapsed high-grade brain tumors. This study combines intravenous nivolumab therapy infused following transient blood-brain barrier opening (BBBO) using low-intensity focused ultrasound with microbubble (LIFU-MB) treatment using NeuroNavigation-Guided Focused Ultrasound (NgFUS).

There are two groups in this study:

  • Group A: Patients with relapsed or progressive diffuse midline glioma in the brainstem
  • Group B: Patients with relapsed or progressive high grade brain tumor that clinically require surgical resection

The primary outcome is to evaluate the safety and feasibility of 3 cycles of nivolumab with BBB disruption using NgFUS with microbubbles in pediatric patients with progressive or relapsed brainstem DMG or with high grade brain tumors after surgery. Secondary outcomes include preliminary efficacy and immunological effects.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

30

Fase

  • Fase 1

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

Luoghi di studio

    • District of Columbia
      • Washington D.C., District of Columbia, Stati Uniti, 20010

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

  • Bambino
  • Adulto

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Age ≥ 3 and ≤ 25 years.
  • Diagnosis of brainstem DMG/DIPG or any high-grade brain tumor.

    • Group A: Relapsed or progressive brainstem DMG.
    • Group B: Relapsed or progressive high-grade intracranial brain tumor requiring surgical resection.
  • Lansky/Karnofsky rating ≥ 60.
  • Patients must have received at least one line of prior therapy upfront for their disease.
  • At least four weeks from radiation therapy, prior immunotherapy, or monoclonal antibody therapy.
  • At least 2 weeks from prior myelosuppressive chemotherapy and post nadir meeting organ function criteria.
  • At least 1 week or 5 half-lives (whichever is longer) from last targeted therapy.
  • If on steroids, stable or decreasing dose for at least 7 days prior to study entry and ≤ 0.4 mg/m2/day of dexamethasone or equivalent.
  • Stable or improving neurological status for 7 days prior to study entry.
  • Organ function:

    • Absolute Neutrophil Count (ANC) ≥750/μL.
    • Absolute Lymphocyte Count (ALC) >500/μL.
    • Platelets ≥75K, unsupported.
    • Coagulation studies: PT and PTT <1.5 ULN and INR (<1.5).
    • Bilirubin ≤1.5x upper limit of normal (ULN).
    • AST/ALT ≤5x ULN.
    • Serum creatinine within normal limits for age.
    • Pulse oximetry >93% on room air.
    • Ejection Fraction (EF) above institutional lower limit of normal (LLN).
  • For females of childbearing potential (FOCBP): negative pregnancy test within 7 days of study entry.
  • Patients of childbearing or child-fathering potential must agree to use contraceptive measures for at least 5 months following nivolumab infusion.
  • Patient or parent/guardian capable of providing informed consent.

Exclusion Criteria:

  • Symptoms and signs of increased intracranial pressure.
  • Patients with metallic ventricular peritoneal shunts. Subjects with nonmetallic VP shunts or similar will have a technical evaluation of the screening non-contrast CT scan of the head. During the mapping of the target area, if the technical NaviFUS specialist determines that the patient cannot be treated within the safety limits of the system, the patient will not be eligible and will be considered a screen failure.
  • Tumor presenting with the following imaging characteristics:

    • Evidence of uncal herniation.
    • Edema and/or mass effect that causes hydrocephalus.
    • Significant areas of necrosis within the tumor that the neurosurgeon feels cannot be avoided during the ultrasound sonication.
    • Evidence of a significant new hemorrhage. Area of microhemorrhage (defined as less than 5 mm in diameter) in the treatment area can be acceptable but requires the review of the neurosurgeon.
    • Containing calcifications in the focused ultrasound sonication beam path and system tools cannot tailor the treatment around these calcification spots.
    • Patients who are deemed to have overly bulky tumor by the PI of the study.
  • The sonication pathway to the tumor involves:

    • More than 30% of the skull area traversed by the sonication pathway is covered by scars, scalp disorders (e.g., eczema), or atrophy of the scalp.
    • Clips, or other non-MRI compatible metallic implanted objects in the skull or the brain, except for shunts.
  • Patients receiving anti-coagulant therapy, or medications known to increase risk of hemorrhage, (e.g., ASA, non-steroidal anti-inflammatory drugs [NSAIDs], statins). There is no required washout for eligibility assessment, but patients should be off agents for at least 3 days at the time of procedure or until 5 half-lives of the agent, whichever is longer.
  • History of a bleeding disorder, coagulopathy or with a history of clinically significant spontaneous tumor hemorrhage.
  • Cerebral or systemic vasculopathy, including intracranial thrombosis, vascular malformation, cerebral aneurysm, or vasculitis.
  • Immunosuppression (corticosteroids to prevent/treat brain edema are permitted).
  • Patients with uncontrolled HIV.
  • Active seizure disorder or epilepsy (clinically significant seizures despite medical treatment) within four weeks prior to first cycle/NaviFUS BBBO procedure captured by history.
  • Known sensitivity to gadolinium-based contrast agents.
  • Known sensitivity to Lumason® ultrasound contrast agent or known hypersensitivity to sulphur hexafluoride microsphere or its components, e.g., polyethylene glycol.
  • Patients unable to fit comfortably into the MRI scanner (generally >250 lbs.).
  • Evidence of cranial or systemic infection.

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: Non randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Group A: Patients with relapsed or progressive diffuse midline glioma in the brainstem
Patients with relapsed or progressive diffuse midline glioma in the brainstem, receiving nivolumab with NgFUS either every 2 weeks or every 4 weeks.
NeuroNavigation-Guided Focused Ultrasound, every 2 or 4 weeks for 3 cycles of 28 days
Lumason is a sulfur hexafluoride microsphere ultrasound contrast agent which will be used as a mechanical resonator. Lumason will be given in combination with NgFUS every 2 or 4 weeks for 3 cycles of 28 days.
Nivolumab is a monoclonal antibody targeting the immune checkpoint axis PD-1/PD-L1. Nivolumab will be given prior to NgFUS with microbubbles (Lumason) every 2 or 4 weeks for 3 cycles of 28 days.
Sperimentale: Group B: Patients with relapsed or progressive high grade brain tumors requiring surgical resection
Patients with relapsed or progressive high grade brain tumors that clinically require surgical resection, receiving one dose of NgFUS prior to surgery, and nivolumab with NgFUS every 4 weeks following recovery from surgery.
NeuroNavigation-Guided Focused Ultrasound, every 2 or 4 weeks for 3 cycles of 28 days
Lumason is a sulfur hexafluoride microsphere ultrasound contrast agent which will be used as a mechanical resonator. Lumason will be given in combination with NgFUS every 2 or 4 weeks for 3 cycles of 28 days.
Nivolumab is a monoclonal antibody targeting the immune checkpoint axis PD-1/PD-L1. Nivolumab will be given prior to NgFUS with microbubbles (Lumason) every 2 or 4 weeks for 3 cycles of 28 days.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence of dose limiting toxicities (DLT) as assessed by CTCAE v6.0.
Lasso di tempo: First treatment through 28 days post-first treatment.
Safety will be evaluated by the incidence of DLTs. DLT is defined as toxicities which are at least possibly related to treatment and meeting protocol-specified criteria for grade, duration, severity, and/or delay of subsequent treatment cycles. If the overall toxicity rate exceeds protocol-specified criteria, enrollment will be halted and the study will be amended to modify the treatment plan.
First treatment through 28 days post-first treatment.
Percentage of patients completing at least two cycles of planned therapy
Lasso di tempo: Enrollment through end of Cycle 2 (each cycle is 28 days).
Treatment will be determined feasible if at least 80% of enrolled patients complete at least 2 cycles of planned therapy. Feasibility will be assessed separately for each cohort.
Enrollment through end of Cycle 2 (each cycle is 28 days).

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall response assessment per RAPNO.
Lasso di tempo: From screening through 1 year post-final treatment.
Overall response assessment: complete response (CR), partial response (PR), minor response (MR), stable disease (SD), or progressive disease (PD) following treatment, will be assessed based on the Response Assessment in Pediatric Neuro-Oncology (RAPNO) scale.
From screening through 1 year post-final treatment.
Progression-free survival (PFS)
Lasso di tempo: From enrollment through up to 2 years post-final treatment.
PFS is defined as the interval of time between the date of protocol treatment initiation and the earliest date of documentation of progressive disease, or second malignancy or death (for any reason) for patients who fail, or to date of last contact or initiation of other therapy for patients who remain at risk of failure.
From enrollment through up to 2 years post-final treatment.
Overall survival (OS)
Lasso di tempo: From enrollment through up to 2 years post-final treatment.
OS post nivolumab infusion will be analyzed by the Kaplan-Meier method.
From enrollment through up to 2 years post-final treatment.

Altre misure di risultato

Misura del risultato
Lasso di tempo
Tissue expression of PD-1 and PD-L1
Lasso di tempo: From enrollment through immediately after surgery.
From enrollment through immediately after surgery.
Lymphocyte counts according to FUS area treated
Lasso di tempo: From enrollment through 3 months post-final treatment.
From enrollment through 3 months post-final treatment.
Immunologic correlates
Lasso di tempo: Pre- and post-procedure starting from enrollment through immediately after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).
Pre- and post-procedure starting from enrollment through immediately after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).
Immunohistochemistry for PD1/PDL1
Lasso di tempo: From enrollment through immediately after surgery.
From enrollment through immediately after surgery.
Immunostaining for lymphocytes
Lasso di tempo: From enrollment through immediately after surgery.
From enrollment through immediately after surgery.
Increase of areas (measured in percentage) of contrast enhancement on T1-gadolinium MRI sequences obtained immediately following BBB disruption.
Lasso di tempo: From enrollment through 36 hours after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).
From enrollment through 36 hours after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).

Collaboratori e investigatori

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

Sponsor

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)

1 settembre 2026

Completamento primario (Stimato)

1 dicembre 2030

Completamento dello studio (Stimato)

1 dicembre 2030

Date di iscrizione allo studio

Primo inviato

20 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

17 giugno 2026

Primo Inserito (Effettivo)

24 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

8 settembre 2026

Ultimo verificato

1 settembre 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

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

Sì

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 .