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NCT01067976 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety of Gadobutrol 1.0 Molar (Gadovist) for Breast MRI

A Phase 3 study, sponsored by Bayer.

Completed
Registry status
Phase 3
Development phase
446
Enrollment target

NCT01067976: Completed Phase 3 study, sponsored by Bayer.

NCT01067976 is a Phase 3 study that has completed, run by Bayer. The registered enrollment target is 446 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01067976, a Phase 3 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 3
Development phase
446 participants
Enrollment target

Study Summary

The purpose of this study is to look at the efficacy (how does it work) and safety of gadobutrol when used for obtaining MR images of both breasts.Women with a recent diagnosis of breast cancer by mammogram (X-ray examination of the breasts) may benefit from MRI of the breasts as MRI may detect additional breast cancers.

Primary Outcome

For a single participant the sensitivity was defined as the proportion of malignant breast regions that were recognized by the clinical investigators and the 3 blinded readers using the respective imaging modality as malignant. Subsequently the sensitivity percentage was calculated based on the mean of the sensitivities across all participants. The difference was calculated as CMRM value minus UMRM value. For ease of expression, the following abbreviations will be used: Magnetic Resonance Mammog

Interventions

  • DRUG Gadobutrol (Gadavist, Gadovist, BAY86-4875)

Trial Details

FieldValue
Enrollment Target 446 participants
Start Date 2010-02
Est. Completion 2012-01
Phase Phase 3
Bayer

591 total trials

What the finished NCT01067976 record still lists

NCT01067976 is an interventional study that assigns participants to a tested intervention. The registered 446 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 (42% lower).

The record links to 0 conditions, and to 1 intervention - of which Gadobutrol (Gadavist, Gadovist, BAY86-4875) is the first listed.

NCT01067976 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01067976 about?

NCT01067976 is a clinical study titled "Efficacy and Safety of Gadobutrol 1.0 Molar (Gadovist) for Breast MRI". The purpose of this study is to look at the efficacy (how does it work) and safety of gadobutrol when used for obtaining MR images of both breasts.Women with a recent diagnosis of breast cancer by mammogram (X-ray examination of the breasts) may benefit from MRI of the breasts as MRI may detect addi...

What is the current status of trial NCT01067976?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 446 participants. The study started on 2010-02. Estimated completion is 2012-01.

What interventions are being tested in trial NCT01067976?

The interventions under investigation include: Gadobutrol (Gadavist, Gadovist, BAY86-4875) (DRUG).

Who is sponsoring clinical trial NCT01067976?

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

How this trial's enrollment target compares

Where NCT01067976's enrollment target sits among peer trials

446 864th of 2000 higher than 1,137 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 NCT01067976, the US trial registry maintained by the National Library of Medicine. NCT01067976 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.