Clinical Trials Logo

Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04307186
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date November 18, 2020
Completion date September 6, 2022

See also
  Status Clinical Trial Phase
Completed NCT00411931 - A Pharmacokinetics Study of MultiHance in Pediatric Patients Phase 1
Completed NCT05915702 - A Study to Compare How Well Gadoquatrane Works and Its Safety With an Already Available Contrast Agent for MRI in People With Known or Suspected Brain or Spinal Cord-related Problems Phase 3