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NCT05057702 · ClinicalTrials.gov registry record · NA

Individualized Treatment Plan in Children and Young Adults With Relapsed Medulloblastoma and Ependymoma

A NA study of Medulloblastoma and Ependymoma, sponsored by University of California, San Francisco.

Recruiting
Registry status
NA
Development phase
74
Enrollment target
8
Study locations

NCT05057702: Recruiting NA study of Medulloblastoma and Ependymoma, sponsored by University of California, San Francisco.

NCT05057702 is a NA study of Medulloblastoma and Ependymoma that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 74 participants, below the 138-participant average among 29 other Medulloblastoma trials with a reported enrollment target (46% lower). The trial reports 8 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05057702, a NA study of Medulloblastoma and Ependymoma, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
NA
Development phase
74 participants
Enrollment target
8
Study locations

Study Summary

The current study will use a new treatment approach based on the molecular characteristics of each participant's tumor. The study will test the feasibility in the pilot phase of performing real-time drug screening on tissue taken during surgery in patients with relapsed medulloblastoma or ependymoma and of having a specialized tumor board assign a treatment plan based on the results of this screening and genomic sequencing. The aim of this trial is to allow every child and young adult with relapsed medulloblastoma and ependymoma to receive the most effective and least toxic therapies currently available and will pave the way for improved understanding and treatment of these tumors in the future. Moreover, if successful, it could serve as a paradigm for personalized medicine programs for other types of cancer.

Primary Outcome

Time to tissue collection will be used to determine the feasibility of using the results of real-time in vitro drug screening, WES and RNAseq of participant-derived specimens to guide treatment recommendations by a specialized tumor board, in a clinically-actionable timeframe, for children and young adults with recurrent medulloblastoma. Participants are expected to receive treatment plan within 21 business days

Interventions

  • OTHER Specialized Tumor Board Treatment Plan
  • OTHER Combinations

Study Locations (8)

California

  • Children's Hospital of Los Angeles - Los Angeles
  • Rady Children's Hospital - San Diego
  • University of California, San Francisco - San Francisco

New York

  • New York University - New York
  • Columbia University Medical Center - New York

District of Columbia

  • Children's National Hospital - Washington D.C.

Missouri

  • St. Louis Children's Hospital / Washington University in St. Louis - St Louis

Pennsylvania

  • Children's Hospital of Philadelphia - Philadelphia

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2022-02-22
Est. Completion 2028-01-31
Phase NA

What NCT05057702 shows while recruiting

NCT05057702 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 138-participant average among 29 other Medulloblastoma trials with a reported enrollment target (46% lower).

The record links to 6 conditions, with Medulloblastoma appearing as the primary indexed condition, and to 2 interventions - of which Specialized Tumor Board Treatment Plan is the first listed.

NCT05057702 lists 8 locations in 5 states (California, New York, District of Columbia).

Frequently Asked Questions

What is clinical trial NCT05057702 about?

NCT05057702 is a clinical study titled "Individualized Treatment Plan in Children and Young Adults With Relapsed Medulloblastoma and Ependymoma". The current study will use a new treatment approach based on the molecular characteristics of each participant's tumor. The study will test the feasibility in the pilot phase of performing real-time drug screening on tissue taken during surgery in patients with relapsed medulloblastoma or ependymoma...

What is the current status of trial NCT05057702?

This trial is currently recruiting. It is a NA study. The enrollment target is 74 participants. The study started on 2022-02-22. Estimated completion is 2028-01-31.

What conditions does trial NCT05057702 study?

This clinical trial studies the following conditions: Medulloblastoma, Ependymoma, Medulloblastoma Recurrent, Medulloblastoma, Childhood, Ependymoma Malignant.

What interventions are being tested in trial NCT05057702?

The interventions under investigation include: Specialized Tumor Board Treatment Plan (OTHER), Combinations (OTHER).

Who is sponsoring clinical trial NCT05057702?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05057702 being conducted?

This trial has 8 study locations across California, District of Columbia, Missouri, New York, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Medulloblastoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05057702's enrollment target sits among peer trials

74 15th of 29 higher than 15 of 29 other Medulloblastoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Medulloblastoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05057702, the US trial registry maintained by the National Library of Medicine. NCT05057702 (small enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.