Clinical Trials Directory

Trials / Completed

CompletedNCT03996447

Efficacy and Safety of Gadopiclenol for Central Nervous System (CNS) Magnetic Resonance Imaging (MRI)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
260 (actual)
Sponsor
Guerbet · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This trial aimed to evaluate the Efficacy and Safety of gadopiclenol for Central Nervous System (CNS) Magnetic Resonance Imaging (MRI)

Detailed description

The purpose of this trial was to evaluate a new gadolinium-based contrast agent (GBCA) gadopiclenol injection for Central Nervous System (CNS) lesion detection and visualization by conventional steady-state CNS imaging. This is a multi-center, international, prospective, double-blind, randomized, controlled, cross-over with comparator trial in male and female patients presenting with known or highly suspected CNS lesion(s) with focal areas of disrupted Blood Brain Barrier (BBB) (e.g., primary and secondary tumors) who are scheduled to undergo a routine contrast-enhanced Magnetic Resonance Imaging (MRI) of the CNS. This trial was conducted in 33 centers worldwide. During the course of the trial, two MRIs were obtained from each patient: one unenhanced and gadopiclenol-enhanced MRI; and one unenhanced and gadobutrol-enhanced MRI. MRI evaluations were performed by on-site investigators and three independent off-site blinded readers.

Conditions

Interventions

TypeNameDescription
DRUGgadopiclenolsingle intravenous (IV) bolus injection at a rate of 2ml/second
DRUGGadobutrol 1Mmol/mL Solution for Injection Vialsingle intravenous (IV) bolus injection at a rate of 2ml/second

Timeline

Start date
2019-06-03
Primary completion
2020-09-11
Completion
2020-09-11
First posted
2019-06-24
Last updated
2025-09-22
Results posted
2025-09-22

Locations

33 sites across 11 countries: United States, Belgium, France, Germany, Hungary, Italy, Mexico, Poland, South Korea, Spain, Taiwan

Regulatory

Source: ClinicalTrials.gov record NCT03996447. Inclusion in this directory is not an endorsement.