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Gadoteridol

DRUG11 trials

Sponsors

Bayer AG, Iqvia Rds France, Bracco Diagnostics, Inc, OHSU Knight Cancer Institute, University of Maryland, Baltimore

Conditions

Anaplastic AstrocytomaBrain DiseaseCentral Nervous System PathologyCognitive FunctionContrast Enhancement in Magnetic Resonance ImagingContrast MediaContrast enhancement in magnetic resonance imaging for assessment of central nervous system pathologyContrast enhancement in magnetic resonance imaging for assessment of non-central nervous system pathology

Early Phase 1

Phase 1

Phase 3

A Study to Compare How Well Gadoquatrane Works and Its Safety With an Already Available Contrast Agent for MRI in People With Any Known or Suspected Problems of the Body (Except Brain or Spinal Cord-related Problems)
CompletedNCT05915728
BayerContrast Enhancement in Magnetic Resonance Imaging, Non-central Nervous System Pathology
Start: 2023-07-24End: 2024-06-01Updated: 2025-12-22
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
CompletedNCT05915702
BayerCentral Nervous System Pathology, Contrast Enhancement in Magnetic Resonance Imaging
Start: 2023-07-24End: 2024-05-31Updated: 2025-08-17
(21197) A multicenter, randomized, prospective double-blind, cross over Phase 3 study to evaluate the efficacy and safety of 0.04 mmol Gd/kg body weight of gadoquatrane for MRI in adults with known or suspected pathology of any body region (except CNS), compared to 0.1 mmol Gd/kg approved macrocyclic gadolinium-based contrast agents (GBCAs)
CompletedCTIS2022-501885-24-00
Bayer AGContrast enhancement in magnetic resonance imaging for assessment of non-central nervous system pathology
Start: 2023-09-20End: 2024-12-20Target: 265Updated: 2024-05-21
(21181) A multicenter, randomized, prospective double-blind, cross over Phase 3 study to evaluate the efficacy and safety of 0.04 mmol Gd/kg body weight of gadoquatrane for MRI in adults with known or suspected pathology of the central nervous system (CNS), compared to 0.1 mmol Gd/kg approved macrocyclic gadolinium-based contrast agents (GBCAs)
CompletedCTIS2022-501884-41-00
Bayer AGContrast enhancement in magnetic resonance imaging for assessment of central nervous system pathology
Start: 2023-09-29End: 2024-12-17Target: 186Updated: 2024-05-21

Phase 4

Unknown Phase

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