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Blood Brain Barrier (BBB) Disruption Using Exablate Focused Ultrasound With Doxorubicin for Treatment of Pediatric DIPG

StatusActive, Not Recruiting
PhasePhase 1/2
SponsorInSightec
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 21, 2026 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Trial status: Recruiting to Active, Not Recruiting Primary completion date: Jan 2026 to Jun 2026 · Completion date: Jul 2026 to Oct 2026 · Site details revisedv6 Show 3 more changesShow less
    • Primary completion date: Jan 2026 to Jun 2026
    • Completion date: Jul 2026 to Oct 2026
    • Site details revised
  2. Notable Enrollment target: 3 to 10 Primary completion date: Jan 4, 2025 to Jan 2026 · Completion date: Jul 4, 2025 to Jul 2026v5 Show 2 more changesShow less
    • Primary completion date: Jan 4, 2025 to Jan 2026
    • Completion date: Jul 4, 2025 to Jul 2026
  3. Minor Re-verified, no change to tracked fieldsv4
  4. Minor Primary completion date: Nov 1, 2024 to Jan 4, 2025 Completion date: May 1, 2025 to Jul 4, 2025 · Start date changed from estimate of Dec 10, 2022 to Jan 4, 2023v3 Show 2 more changesShow less
    • Completion date: May 1, 2025 to Jul 4, 2025
    • Start date changed from estimate of Dec 10, 2022 to Jan 4, 2023
  5. Notable Start date: Nov 1, 2022 to Dec 10, 2022v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
42 trials monitored
See 1 trial at risk
The purpose of this study is to evaluate the safety and efficacy of targeted blood brain barrier disruption with Exablate Model 4000 Type 2.0/2.1 in combination with Doxorubicin therapy for the treatment of DIPG in pediatric patients
Trial Details
NCT Number NCT05615623
Lead Sponsor InSightec
Conditions Brain Tumor
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov