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Preliminary Clinical Feasibility Study of a Medical Device Enabling Brain Access Using Microbubble-Enhanced Sonication (CAMPSIS)

6 agosto 2026 aggiornato da: Gustave Roussy, Cancer Campus, Grand Paris

Cerebral Access Using Microbubble Potentiated Sonication: Initial Study

CAMPSIS is a preliminary feasibility study of the TheraOne medical device (IIb). TheraOne is an active, non-invasive medical device intended to deliver transcranial FUS in combination with intravenous microbubbles in order to transiently and locally induce the BBB permeability.

This study aims to evaluate the safety of cerebral sonication (TheraOne) in the management of patients with recurrent grade 4 glioma (wild-type IDH, technically resectable) or brain metastases originating from an extracranial solid tumor.

Patients enrolled in the study will undergo a single sonication session during a protocol visit and will be monitored for up to 30 days after the sonication through the various scheduled protocol visits.

Blood samples will be collected at the start of the study, during the sonication, and during the post-sonication follow-up visit for all patients enrolled in the study.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

6

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

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:

  1. Age: ≥18 years old.
  2. Performance Status: Karnofsky Performance Score (KPS) ≥ 70%.
  3. Tumor Characteristics:

    1. Patient with an expansive intra-cerebral tumor showing enhancement after gadolinium injection on MRI (T1-weighted images, with and without gadolinium contrast).
    2. Tumor radiologically classified as:

      • Recurrent High-Grade glioma (excluding prosthetic material), or a brain metastasis from extracranial solid primary.
      • Measuring at least 25-30 mm in the longest axis.
      • In both cases, Surgery is not required as a first-line option. However, the target lesion must be considered technically operable (non-eloquent location)
    3. In the case of brain metastases, multifocal disease is allowed, provided that additional metastases are smaller to 20 mm, not neurologically threatening, and do not require surgery. Cases of leptomeningeal invasion are not allowed.
    4. Tumor should not exhibit signs of rapid progression or acute neurological compromise requiring urgent intervention. Rapid progression is defined as a ≥25% increase in contrast-enhancing tumor volume within 4 weeks, associated with mass effect or new edema. Acute neurological compromise includes any newly developed or worsening neurological deficit (e.g., motor weakness, aphasia), seizures refractory to antiepileptics, decreased level of consciousness (Glasgow Coma Scale (GCS) <13), or signs of intracranial hypertension.
  4. Operability and Location:

    • Target Tumor is deemed operable by the neurosurgeon and is located in a non-eloquent area (e.g., excluding brainstem or regions associated with critical motor or speech function).
    • Tumor must be located in the cortical or subcortical regions, at least 20 mm beneath the inner skull surface to ensure accessibility to the TheraOne intervention.
  5. In case of brain metastasis, extracerebral disease must be absent or at least controlled, defined as:

    • A Positron Emission Tomography (PET) scan performed within 6 weeks showing resolution of hyperintensity, or
    • Stable disease on two consecutive imaging assessments
    • And oligometastatic state, defined as ≤3 extracerebral lesions.
  6. Blood Pressure Stability : Systolic ≤180 mmHg, Diastolic ≤100 mmHg at screening.
  7. Coagulation Stability :

    • Platelets ≥80.10 9 /L
    • Prothrombin time (PT) ≤14 sec
    • Partial thromboplastin time (PTT) ≤36 sec
    • International Normalized Ratio (INR) ≤1.3
  8. Prior and ongoing treatments

    • Prior systemic anticancer treatments are allowed provided that all the following conditions are met:

      • The patient has a clinically stable neurological status at inclusion.
      • There is no ongoing ≥ Grade 2 neurological toxicity attributable to prior or ongoing systemic treatment.
      • Corticosteroid dose is stable or decreasing for at least 7 days prior to inclusion.
    • The following minimum wash-out periods prior to sonication must be respected:

      • Immunotherapy (anti-PD-1, anti-PD-L1, anti-CTLA-4): ≥ 7 days before sonication.
      • Nitrosourea-containing chemotherapy (BCNU, CCNU): ≥ 6 weeks before sonication.
      • Targeted therapies - lung cancer (EGFR, ALK, ROS1, MET TKIs): Wash-out corresponding to 5 terminal half-lives, capped at a maximum of 7 days, provided neurological stability and absence of recent treatment initiation or dose escalation.
      • Targeted therapies - melanoma (BRAF and/or MEK inhibitors): A short pragmatic wash-out of approximately 5-7 days, not strictly based on pharmacokinetic half-life, may be applied provided neurological status is stable and no ≥ Grade 2 neurological toxicity is present.
      • Anti-angiogenic therapy (bevacizumab):

    A minimum interval of 7 days prior to sonication is required.

    • Antibody-drug conjugates (ADCs): A wash-out of 7 days prior to sonication is required. ADC treatment must be ongoing (not recently initiated), with no ≥ Grade 2 toxicity, particularly neurological or hematological.
    • Antiplatelet and anticoagulant agents: Must be discontinued according to the following minimum intervals prior to sonication:

      • antiplatelet agents: ≥ 7 days
      • vitamin K antagonists: ≥ 7 days
      • direct oral anticoagulants (NOACs): ≥ 72 hours
      • heparin-derived compounds: ≥ 48 hours

        • Prior brain radiotherapy is allowed provided it was completed ≥ 12 weeks before sonication
  9. Renal Function: Estimated glomerular filtration rate (eGFR) ≥30 mL/min/1.73m².
  10. MRI & CT Compatibility: Patient must be able to complete high-density CT and MRI studies, including contrast-enhanced imaging.
  11. Procedure Feasibility :

    • Willingness to undergo partial head shaving to allow proper ultrasound transmission
    • Ability to maintain stable seated position during procedure.
  12. Negative Serum Pregnancy Test (within 7 days before first treatment) for women of childbearing potential.
  13. Contraceptive Use: Women of childbearing potential and men with partners of childbearing potential must agree to use a highly effective (<1% failure rate per year) approved contraceptive method during procedure and for 6 months post- procedure. A woman is considered of childbearing potential (WOCBP), i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy.
  14. Signed Informed Consent Form.
  15. Patients must be affiliated or beneficiary to a social security system

Exclusion Criteria:

  1. Tumor-Related Exclusions:

    • Tumor imaging features suggestive of:

      • Acute mass effect with ≥5 mm midline shift or basal cistern effacement.
      • Severe peritumoral edema causing acute intracranial hypertension or compression of critical structures.
      • Hemorrhagic transformation or necrosis with a high risk of rupture.
    • Tumor morphology or imaging findings that preclude the ability to sonicate the tumor volume, including:

      • Significant tumor volume outside the treatment envelope.
      • Tumor volume exceeding the maximum allowed sonication volume (currently 110 ccs at the treatment volume level).
      • Concerns about adequate tumor coverage by sonication based on tumor morphology should be discussed with the Sponsor.
  2. Vascular & Hemorrhagic Conditions:

    • Cerebrovascular disease history:

      • Untreated arteriovenous malformation (AVM).
      • Untreated or unstable cerebral aneurysm.
    • Acute hemorrhage or cystic lesions:

      • Evidence of acute intracranial hemorrhage.
      • Presence of a cyst within the region of interest (ROI).
    • MRI or clinical findings of:

      • Active or chronic infections/inflammatory processes.
      • Acute or chronic hemorrhages, lobar microbleeds, siderosis, amyloid angiopathy, or macro-hemorrhages.
      • Intracranial thrombosis, vascular malformation, cerebral aneurysm, or vasculitis.
  3. Cardiovascular & Systemic Conditions:

    • Unstable cardiac disease or hemodynamic status.
    • Uncontrolled severe hypertension (systolic >180 mmHg, diastolic >100 mmHg).
  4. Anticoagulation & Bleeding Risks:

    • Use of medications that increase bleeding risk:

      • Antiplatelet agents (e.g., aspirin, clopidogrel) within 7 days prior to treatment.
      • Anticoagulants (e.g., warfarin, dabigatran, apixaban, heparin) within specified washout periods:

        • Oral vitamin K inhibitors: 7 days
        • Non-Vitamin K antagonist oral anticoagulants (NOACs) (e.g., rivaroxaban, apixaban): 72 hours
        • Heparin-derived compounds: 48 hours
    • Abnormal coagulation profile: Platelets <80,000 109/L, PT >14, PTT >36, INR >1.3.
    • History of bleeding disorder, coagulopathy, or spontaneous hemorrhage.
  5. Neurological & Psychiatric Conditions:

    • Active seizures (>1 per week) despite medication, as BBB opening could worsen seizures.
    • Active drug/alcohol disorder, increasing seizure, infection, or compliance risks.
    • Known positive Human Immunodeficiency Virus (HIV) status, which may increase BBB permeability and lead to encephalitis.
    • Potential blood-borne infections that could increase risk of meningitis or brain abscess.
  6. Prior treatments incompatible with study participation

    • Any immunotherapy administered within 7 days prior to sonication.
    • Any nitrosourea-containing chemotherapy administered within 6 weeks prior to sonication.
    • Any targeted therapy not meeting the wash-out and stability criteria described above.
    • Any antibody-drug conjugate administered within 7 days prior to sonication or associated with ongoing ≥ Grade 2 toxicity.
    • Any experimental therapy or investigational medicinal product not discontinued ≥ 30 days prior to sonication.
    • Brain radiotherapy completed < 12 weeks prior to sonication
  7. Imaging & Gadolinium Contraindications:

    • Severe claustrophobia or inability to remain supine for 2 hours.
    • Body habitus incompatible with CT or MRI scanner limits
    • Known allergy(ies) or hypersensitivity to gadolinium contrast agents.
    • MRI-incompatible implanted device (e.g., pacemaker, defibrillatore, cochlear implant)
    • Ferromagnetic foreign body
  8. Contraindications to Microbubble Use:

    • Hypersensitivity to sulfur hexafluoride microbubbles or any excipient
    • History of severe allergic reactions (anaphylaxis) to contrast agents.
    • Right-to-left cardiac shunt or embolization risk.
    • Severe pulmonary hypertension or unstable cardiac conditions (e.g. unstable ischemic heart disease, acute coronary syndrome within the previous 30 days).
    • Uncontrolled systemic hypertension,
    • Adult respiratory distress syndrome (ARDS)
    • Any SmPC-listed contraindication
  9. Contraindications/ constraints from associated non-experimental devices :

    • Ultrasound gel :

      • Known hypersensitivity to any component of the ultrasound gel used during the procedure
    • Cervical collar (PATRIOT) , contraindications per IFU

      • Compromised airway,
      • Known severe spinal deformity (e.g., ankylosing spondylitis),
      • Penetrating trauma injuries (cervical).
    • Positionning chair :

      • Inability to maintain a stable seated position for the duration of the procedure.
  10. Other Procedure-Related Exclusions:

    • Presence of metallic implants (e.g., clips in skull/brain) interfering with sonication.
    • Scalp infection at target site
  11. Psychological, Social & Legal Factors:

    • Mental health disorders or social/geographical barriers that could affect CI compliance.
    • Patients under legal protection, guardianship, or deprived of liberty.
  12. Pregnancy & Breastfeeding:

    • Pregnant or breastfeeding women, or those planning pregnancy during the CI and 6 months after.

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: Altro
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Patients with recurrent grade 4 glioma or brain metastasis from an extracranial solid tumor
TheraOne is an active, non-invasive medical device intended to deliver transcranial FUS in combination with intravenous microbubbles in order to transiently and locally induce the BBB permeability.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Safety : evaluating the occurrence and severity of adverse events related to the sonication procedure
Lasso di tempo: Up to 14 days after the sonication
Up to 14 days after the sonication

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Feasibility : completion rate of sonication phase
Lasso di tempo: Immediately after the procedure.
Immediately after the procedure.
BBB permeability assessment by several MRI imaging at predefined timepoints.
Lasso di tempo: Up to 14 days after the sonication
Up to 14 days after the sonication

Collaboratori e investigatori

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

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 settembre 2027

Completamento dello studio (Stimato)

1 ottobre 2027

Date di iscrizione allo studio

Primo inviato

3 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

6 agosto 2026

Primo Inserito (Effettivo)

10 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

10 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

6 agosto 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 2025-A02389-40
  • 2026/4280 (Altro identificatore: CSET number (Gustave Roussy ID))

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

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 .

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