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NCT05915702 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by Bayer.

Completed
Registry status
Phase 3
Development phase
303
Enrollment target

NCT05915702: Completed Phase 3 study, sponsored by Bayer.

NCT05915702 is a Phase 3 study that has completed, run by Bayer. The registered enrollment target is 303 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05915702, a Phase 3 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 3
Development phase
303 participants
Enrollment target

Study Summary

Researchers are looking for a better way to help people with known or suspected brain or spinal cord-related problems scheduled for a "contrast-enhanced" Magnetic Resonance Imaging (MRI). MRI is used by doctors to create detailed images of the inside of the body to identify health problems. Sometimes doctors need to inject a contrast agent into a patient's vein to perform a so called "contrast-enhanced" MRI (CE-MRI). Such CE-MRI examinations may support doctors to identify certain health problems or improve the evaluation. The contrast agents commonly used in MRI are gadolinium-based contrast agents (GBCAs). GBCAs contain a "rare earth" element called gadolinium (Gd). Gadoquatrane is a new contrast agent under development with a lower amount of Gd needed per CE-MRI. The main purpose of this study is to learn whether CE-MRI scans with gadoquatrane work better than MRI scans without the use of a contrast agent (GBCA). The researchers will compare the ability to detect brain and spinal cord-related problems in gadoquatrane-MRI scans to plain-MRI scans without the use of a contrast agent. The participants will undergo 2 MRI scans, one with gadoquatrane and one with currently used GBCA. Both contrast agents will be injected into the vein. Each participant will be in the study for between 6 and 42 days with up to 7 doctor visits. At the start or during the study, the doctors and their study team will: * take blood and urine samples * do physical examinations * check blood pressure and heart rate * review the MRI scans obtained in the study and decide on the diagnosis * ask the participants questions about how they are feeling and what adverse events they are having. An adverse event is any medical problem that a participant has during a study. Doctors keep track of all adverse events, irrespective if they think it is related or not to the study treatments.

Primary Outcome

Contrast Enhancement will be assessed on a 4-point scale (1/No: not enhanced, 2/Moderate: weakly enhanced, 3/Good: clearly enhanced, 4/Excellent: clearly and brightly enhanced). BICR = blinded independent central read / blinded independent central readers; MRI = magnetic resonance imaging

Interventions

  • DRUG Gadobutrol
  • DRUG Gadoteridol
  • DRUG Gadoterate meglumine
  • DRUG Gadoquatrane (BAY1747846)

Trial Details

FieldValue
Enrollment Target 303 participants
Start Date 2023-07-24
Est. Completion 2024-05-31
Phase Phase 3
Bayer

591 total trials

What the finished NCT05915702 record still lists

NCT05915702 is an interventional study that assigns participants to a tested intervention. The registered 303 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 4 interventions - of which Gadobutrol is the first listed.

NCT05915702 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05915702 about?

NCT05915702 is a clinical study titled "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". Researchers are looking for a better way to help people with known or suspected brain or spinal cord-related problems scheduled for a "contrast-enhanced" Magnetic Resonance Imaging (MRI). MRI is used by doctors to create detailed images of the inside of the body to identify health problems. Sometim...

What is the current status of trial NCT05915702?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 303 participants. The study started on 2023-07-24. Estimated completion is 2024-05-31.

What interventions are being tested in trial NCT05915702?

The interventions under investigation include: Gadobutrol (DRUG), Gadoteridol (DRUG), Gadoterate meglumine (DRUG), Gadoquatrane (BAY1747846) (DRUG).

Who is sponsoring clinical trial NCT05915702?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05915702's enrollment target sits among peer trials

303 1119th of 2000 higher than 882 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05915702, the US trial registry maintained by the National Library of Medicine. NCT05915702 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.