CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 57 enrolled
Drug / intervention
Gadoquatrane (BAY1747846) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04307186
NCT04307186Phase 2Completed

Multicenter, Single-blind, Adaptive Dose Finding Study of Single Intravenous Injections of BAY 1747846 With Corresponding Blinded Read in Adult Participants With Known or Highly Suspected CNS Lesions Referred for Contrast-enhanced MRI of the CNS

Bayer·interventional·Posted Mar 13, 2020·Updated Nov 15, 2023

In Brief

A Phase 2 clinical trial evaluating Gadoquatrane (BAY1747846) and Gadobutrol (Gadovist/Gadavist) for Central Nervous System Pathology. Completed, enrolled 57 participants across 17 sites in 4 countries.

Detailed Summary

Researchers in this study want to find the appropriate dose of drug BAY1747846 for adults undergoing MRI for known or highly suspected brain and/or spinal cord conditions so that the image quality is similar to that of drug gadobutrol for adults undergoing MRI. MRI stands for Magnetic resonance imaging which produces body pictures created by using magnetic energy rather than x-ray energy. Both BAY1747846 and gadobutrol are medicinal products known as gadolinium-based contrast agents (GBCA) which are used in MRI examinations to provide contrast enhancement and improve imaging performance. Gadobutrol (brand name: Gadavist, Gadovist) has been approved worldwide for the diagnosis of various disorders in adult and pediatric patients. BAY1747846 is a new GBCA under development with the goal to provide similar imaging performances in MRI. Participants in this study will receive both BAY1747846 and gadobutrol with a period of 3 - 14 days in between. A MRI examination will be performed after each injection. Participant will stay in this study for 2 - 4 weeks depending on the scheduling of the visits.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBulgaria, Germany, Japan, United States
Collaborators--

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedMar 13, 2020
Enrollment StartNov 18, 2020
Primary CompletionSep 5, 2022
Study CompletionSep 6, 2022
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 6.3 years ago

Interventions

Gadoquatrane (BAY1747846)drug

Solution for IV injection, single dose

Gadobutrol (Gadovist/Gadavist)drug

Solution for IV injection, single dose