MedPath
EMA Approval

Vueway

V08CA12

gadopiclenol

Paramagnetic contrast media

Gadopiclenol

Magnetic Resonance Imaging

Basic Information

EMA regulatory identification and product classification information

EMA Identifiers

ATC CodeV08CA12
EMA European Classification

Overview Summary

Comprehensive product overview and regulatory summary

Vueway is a ‘contrast agent’, a medicine used to improve the contrast of images obtained during magnetic resonance imaging (MRI) examinations. This helps doctors find certain pathologies in patients in whom this would not be possible otherwise. Vueway is used in adults and children from 2 years of age.

Vueway contains the active substance gadopiclenol.

Authorisations (1)

EMEA/H/C/006172

Bracco Imaging S.p.A.,Via Egidio Folli 50,20134 Milan,ITALY

Authorised

December 7, 2023

Active Substances (1)

Gadopiclenol

Documents (10)

CHMP summary of positive opinion for Vueway

October 13, 2023

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

CHMP summary of positive opinion for Vueway

October 13, 2023

CHANGES_SINCE_INITIAL_AUTHORISATION

Vueway : EPAR - Public assessment report

February 13, 2024

CHANGES_SINCE_INITIAL_AUTHORISATION

Vueway : EPAR - Public assessment report

February 13, 2024

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Vueway : EPAR - Medicine overview

February 13, 2024

OVERVIEW_DOCUMENT

Vueway : EPAR - Risk management plan

February 13, 2024

RISK_MANAGEMENT_PLAN_SUMMARY

Vueway-H-C-PSUSA-00000232-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

February 4, 2025

CHANGES_SINCE_INITIAL_AUTHORISATION

Vueway : EPAR - Product information

February 13, 2024

DRUG_PRODUCT_INFORMATION

Vueway : EPAR - All authorised presentations

February 13, 2024

AUTHORISED_PRESENTATIONS

Vueway : EPAR - Procedural steps taken and scientific information after authorisation

August 21, 2024

CHANGES_SINCE_INITIAL_AUTHORISATION

Overview Q&A (7)

Question

How is Vueway used?

Answer

Vueway is given as an injection into a vein by a specialised healthcare professional, just before the MRI scan. It can only be obtained with a prescription. For more information about using Vueway, see the package leaflet or contact your doctor or pharmacist.

Question

Other information about Vueway

Answer

Vueway received a marketing authorisation valid throughout the EU on 07 December 2023.

Question

How does Vueway work?

Answer

The active substance in Vueway, gadopiclenol, contains gadolinium, a ‘rare-earth’ metal element used in contrast agents to help obtain better MRI images. MRI is an imaging method that relies on the tiny magnetic fields produced by water molecules in the body. Once injected, gadolinium interacts with the water molecules. As a result of this interaction, the water molecules give a stronger signal in the locations reached by the contrast agent, and this helps to obtain a brighter picture.

Question

What benefits of Vueway have been shown in studies?

Answer

Two main studies were carried out to investigate whether MRI images made with Vueway were comparable to those made with another contrast agent, and better than those made without a contrast agent. One study involved 256 adults who had, or were highly suspected to have, a tumour in their brain or spinal cord, based on the outcome of a previous imaging procedure (such as an MRI or CT scan). The second study involved 304 adults with a tumour or other pathological tissue (such as a cyst) in another part of their body.

Study participants had MRI scans in combination with Vueway, in combination with another gadolinium-based contrast agent and without a contrast agent. Doctors experienced in analysing MRI images then compared how clearly the tumours or pathologies were visible in the different scans. All doctors considered that MRI images with Vueway were clearer than those made without a contrast agent, and comparable with those made with the other contrast agent.

Question

What are the risks associated with Vueway?

Answer

For the full list of side effects and restrictions with Vueway, see the package leaflet.

The most common side effects with Vueway (which may affect up to 1 in 10 people) include headache and injection site reactions. Other common side effects (which may affect up to 1 in 100 people) include nausea, fatigue and diarrhoea.

Question

Why is Vueway authorised in the EU?

Answer

Using Vueway as a contrast agent improved the quality of the resulting MRI scan compared to an unenhanced scan. The safety profile of Vueway is in line with that of other gadolinium-based contrast agents. Importantly, Vueway contains gadolinium in a specific complex. This means that it can be given at half the dose of gadolinium compared with other, non-specific gadolinium-containing contrast agents while providing the same contrast enhancement. The European Medicines Agency therefore decided that Vueway’s benefits are greater than its risks and it can be authorised for use in the EU.

Question

What measures are being taken to ensure the safe and effective use of Vueway?

Answer

Recommendations and precautions to be followed by healthcare professionals and patients for the safe and effective use of Vueway have been included in the summary of product characteristics and the package leaflet.

As for all medicines, data on the use of Vueway are continuously monitored. Suspected side effects reported with Vueway are carefully evaluated and any necessary action taken to protect patients.

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