Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07512154

Precision Radiotherapy Enabled by Molecular MRI

Led by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Updated on 2026-05-06

20

Participants Needed

1

Research Sites

313 weeks

Total Duration

On this page

Sponsors

S

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Lead Sponsor

T

The Ben & Catherine Ivy Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a research study to determine if a novel molecular magnetic resonance imaging (MRI) technique, called amide proton transfer (APT) imaging, is useful in identifying the most aggressive areas of tumor needed for radiotherapy of brain tumors.

CONDITIONS

Official Title

Precision Radiotherapy Enabled by Molecular MRI

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologic confirmation of glioblastoma or grade 4 astrocytoma
  • Age over 18 years
  • Karnofsky Performance Status (KPS) of at least 60
  • Normal organ and marrow function including leukocytes > 3,000/mcL, absolute neutrophil count > 1,500/mcL, platelets > 100,000/mcL
  • Total bilirubin within normal institutional limits
  • AST/ALT less than 2.5 times institutional upper limit of normal
  • Creatinine within normal institutional limits or creatinine clearance > 60 mL/min/1.73 m2 if creatinine elevated
  • Patients of child-bearing potential must use adequate contraception
  • Ability and willingness to sign informed consent
Not Eligible

You will not qualify if you...

  • Inability to receive MRI scans
  • Receiving other investigational cancer treatments at enrollment
  • Previous overlapping brain radiotherapy treatment
  • Uncontrolled illness such as active infection, symptomatic heart failure, unstable angina, cardiac arrhythmia, or psychiatric/social conditions limiting study compliance
  • Pregnant or breastfeeding women
  • Women of child-bearing potential unwilling or unable to use effective birth control during study and 12 weeks after
  • Male subjects unwilling to use effective contraception during study and 12 weeks after

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Johns Hopkins University

Baltimore, Maryland, United States, 21287

Actively Recruiting

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Research Team

K

Kristin Redmond

CONTACT

R

Ryan Manuel

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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