Ultrasound 'Key' may let chemo reach Kids' brain tumors
NCT ID NCT05293197
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-stage trial tests whether a device called SonoCloud-9 can safely open the blood-brain barrier in children aged 5 to 17 with recurrent malignant brain tumors. The barrier normally blocks chemotherapy from reaching the brain. By using low-intensity ultrasound just before giving the drug carboplatin, researchers hope to boost treatment effectiveness. The study involves 24 participants and focuses on safety, including risks like bleeding or seizures.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- carboplatin (chemotherapy) delivered after ultrasound opening of the blood-brain barrier using the SonoCloud-9 device
- What this could lead to
- If it works, this could make chemotherapy more effective for children with hard-to-treat brain tumors by temporarily opening the blood-brain barrier.
- What could go wrong
- This is a very early (Phase 1) safety trial with only 24 children, so it may not improve survival. Risks include bleeding, brain swelling, or seizures from the ultrasound procedure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Feb 2023
- Expected to finish
-
Oct 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
5 to 17 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patient aged ≥ 5 years old and \< 18 years old * patient able to receive sonications and perform MRI studies without sedation * diagnosis of supra-tentorial primary malignant brain tumor (e.g. malignant glioma, embryonal tumor including ATRT, ependymoma) * recurrence or progression of brain tumor after at least a first line of standard treatment (multifocal tumors and metastatic disease allowed) * indication of treatment with carboplatin, validated in multidisciplinary meeting * Karnofsky performance scale index (patients ≥ 16 years old) or Lansky performance status (patients \< 16 years old) \> 50% (a patient with a performance status score altered by a motor deficit due to tumor infiltration will be allowed to be included) * no threat of brain herniation or uncontrolled intracranial hypertension * corticosteroids treatment ≤ 1mg/kg/day * neutrophils \> 1.5 x 109/L * platelets \> 100 x 109/L * total bilirubin \< 1.5x upper limit of normal, AST et ALT \< 2.5x upper limit of normal * serum creatinin \< 1.5x upper limit of normal for the age or creatinine clairance \>70mL/min/1.73m2 (EDTA method or 24h urine) * coagulation parameters in the normal limits for age (fibrinogen, prothrombin time and activated clotting time) * no grade 2 or more toxicity depending on the NCI-CTCAE v5.0 criteria * no healed wound on the scalp * covered by health insurance * for patients of chilbearing age (15-17 years old) : a negative pregnancy test and an efficient method of birth control * written consent signed by the patient (if possible) and his parents or legal representatives. Exclusion Criteria: * weight \<15kg * significant intra-tumoral bleeding (hematoma) or ipsilateral subdural effusion * antineoplastic treatment other than carboplatin taken at the same time or stopped since less than: * 6 weeks for nitrosoureas * 1 month for temozolomide * 1 month for bevacizumab * 5 half-lives for tyrosin kinase inhibitors * 3 weeks for any other chemotherapy for the first sonication session * radiotherapy during the last 6 weeks * any other cancer treated during the last 5 years * any other uncontrolled disease or active infection * any other co-morbidity that could compromise participation to the study (in the judgement of the clinical investigator) * any anatomical particularity (skull thickness, thin skin) that could compromise a safe implantation of the device and/or compromise the quality of the treatment (in the judgement of the clinical investigator) * implanted defibrillator/pacemaker, neurostimulator, cochlear implant, intracerebral ferromagnetic vascular clip * any contraindication to general anesthesia * any contraindication to MRI or known allergy to gadolinium or other MRI contrast agent/ * any contraindication to ultrasound contrast agent: * allergy to the active substance or any excipient * acute coronary syndrome or uncontrolled ischemic heart disease * chronic heart failure or history of acute heart failure or heart failure grade III or IV * treatment with dobutamine * severe pulmonary arterial hypertension * uncontrolled systemic hypertension * respiratory distress syndrome * carboplartin hypersensitivity * treatment with phenytoin or fosphenytoin * earlier vaccination with attenuated alive vaccine * diminished auditory acuity ≥ grade 3 on CTCAE classification * history of thermoregulation disorder * impossibility of a rigorous medical follow-up due to geographic, social or mental reasons * pregnant and lactating women * contemporaneous treatment by anticoagulant or platelet aggregation inhibiting drugs * contemporaneous treatment possibly toxic for the central nervous system. The following treatments are excluded if taken less than 5 half-lives before the ultrasound session (unknown toxicity in case of BBB disruption) : * benzodiazepine (or any sedative or hypnotique drug) * antihistamine * proconvulsant drugs * butyrophenone, phenothiazine, or any "conventional" antipsychotic drug * barbiturate * MAO inhibitor * anticholinergic * anticoagulant * any contemporaneous treatment that, in the judgement of the clinical investigator, could induce brain toxicity after BBB disruption
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Atypical teratoid/rhabdoid tumor are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
3 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Institut Curie
RECRUITINGParis, 75005, France
-
Institut Gustave Roussy
RECRUITINGVillejuif, 94800, France
-
Service de neurochirugie Pédiatrique - Hôpital Necker- Enfants Malades
RECRUITINGParis, 75015, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Radioactive gel aimed straight at childhood brain tumors
- Can a RAGE inhibitor tame brain swelling after tumor surgery?
- Can new PET scans guide brain tumor catheters more precisely?
- Can an immune booster fight rare brain tumors?
- Can trained immune cells outsmart brain tumors?
- Can an AI app give a voice to brain tumor patients?