drugset / Trial / NCT02633501

P03277 Dose Finding Study in Central Nervous System (CNS) Magnetic Resonance Imaging (MRI)

NCT02633501

Phase 2 Completed 312 enrolled Guerbet
RandomizedParallel-groupQuadruple-blindDiagnostic

Summary

The purpose of this study was to determine a safe and effective dose of a new gadolinium-based contrast agent (GBCA) P03277 based on the Contrast to Noise Ratio (CNR) when comparing with gadobenate dimeglumine (MultiHance®) at 0.1 mmol/kg body weight (BW). Contrast to Noise Ratio (CNR), a well-known quantitative parameter directly related to contrast medium/GBCA efficacy, was chosen as the primary endpoint in order to have a precise determination of P03277 clinical dose. This was a multi-center, international, prospective, double-blind, randomized, controlled, parallel dose groups, cross-over with comparator study in male and female subjects presenting with known or highly suspected focal areas of disruption of the Blood Brain Barrier including at least one expected enhancing lesion of minimum 5 mm, who were scheduled to undergo a routine contrast-enhanced Magnetic Resonance Imaging (MRI) of Central Nervous System.

Timeline

Start
2016-06
Primary completion
2018-01
Completion
2018-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Gadobenate dimeglumine Diagnostic / imaging agent 0.1 unknown Intravenous
Subject Gadopiclenol Diagnostic / imaging agent 0.025 unknown Intravenous
Subject Gadopiclenol Diagnostic / imaging agent 0.05 unknown Intravenous
Subject Gadopiclenol Diagnostic / imaging agent 0.1 unknown Intravenous
Subject Gadopiclenol Diagnostic / imaging agent 0.2 unknown Intravenous

Indications

No indication recorded.