RecruitingNot ApplicableNCT07415018

Optimizing Contrast Dose and Scanning Parameters for Detection of Leptomeningeal Disease


Sponsor

M.D. Anderson Cancer Center

Enrollment

40 participants

Start Date

Jun 10, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if gadopiclenol (a contrast agent) used during MRI scanning can help in the detection of early LMD.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Patients with tissue confirmed solid malignancy and standard of care brain MRI with equivocal results for LMD (questionable or possible) and negative LP CSF sampling or patients with high risk clinical LMD and negative brain MR and LP CSF sampling. Initially, we will target solid tumors, but if more patients are needed to meet the study power we will enroll liquid tumors.
  • Participants > 18 years of age.
  • Participants are able to consent.

Exclusion Criteria4

  • Participants with CSF sampling positive for LMD or MR brain/spine with definitive evidence of LMD.
  • Participants with implantable devices that can not be scanned with MR safe mode for participant safety.
  • Pregnant participants or potentially pregnant participants are at risk of contrast on the fetus
  • Pediatric participants < 18 years of age.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

PROCEDUREMRI Scan

Given during standard of care

DRUGVUEWAY

Given by IV

DRUGGadavist

Given by IV


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07415018


Related Trials