MedPath
EMA Approval

Cuprior

A16AX

各种消化道产物及代谢产物

Other alimentary tract and metabolism products

Basic Information

EMA regulatory identification and product classification information

EMA Identifiers

ATC CodeA16AX
EMA European Classification

Overview Summary

Comprehensive product overview and regulatory summary

This is a summary of the European public assessment report (EPAR) for Cuprior. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Cuprior.

For practical information about using Cuprior, patients should read the package leaflet or contact their doctor or pharmacist.

Authorisations (1)

EMEA/H/C/004005

Orphalan,226 Boulevard Voltaire,75011 Paris,France

Authorised

September 5, 2017

Active Substances (1)

Trientine tetrahydrochloride

Documents (9)

Cuprior : EPAR - Public assessment report

October 3, 2017

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Cuprior : EPAR - Product Information

October 3, 2017

DRUG_PRODUCT_INFORMATION

Cuprior-H-C-PSUSA-00010637-201809 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

July 24, 2019

CHANGES_SINCE_INITIAL_AUTHORISATION

Cuprior : EPAR - All Authorised presentations

October 3, 2017

AUTHORISED_PRESENTATIONS

CHMP summary of positive opinion for Cuprior

April 21, 2017

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Cuprior : EPAR - Procedural steps taken and scientific information after the authorisation

November 6, 2018

CHANGES_SINCE_INITIAL_AUTHORISATION

Cuprior : EPAR - Summary for the public

October 3, 2017

OVERVIEW_DOCUMENT

Cuprior : EPAR - Public assessment report

October 3, 2017

CHANGES_SINCE_INITIAL_AUTHORISATION

CHMP summary of positive opinion for Cuprior

April 21, 2017

CHANGES_SINCE_INITIAL_AUTHORISATION

Overview Q&A (8)

Question

How is Cuprior used?

Answer

Cuprior can only be obtained with a prescription and treatment should be started by a specialist with experience in the management of Wilson's disease.

Cuprior is available as 150 mg tablets. In adults, the total recommended daily dose is from 3 to 6.5 tablets, and in children from 1.5 to 4 tablets. The tablets are taken in 2 to 4 divided doses. Doses are adjusted according to patient response and levels of copper in the body. Cuprior should be taken on an empty stomach, at least one hour before or two hours after meals.

For further information, see the package leaflet.

Question

How does Cuprior work?

Answer

The active substance in Cuprior, trientine, is a chelating agent. It works by attaching to copper in the body and forming a complex that is then eliminated in the urine.

Question

How has Cuprior been studied?

Answer

The company provided data from the published literature, which show that trientine significantly increases copper elimination in the urine.

The company also carried out a study to compare the levels of trientine in the blood after having taken Cuprior with those for the reference medicine. Results showed that Cuprior produces higher levels of the active substance in the blood than the reference medicine. To take account of this difference, Cuprior is used at lower doses.

Question

What are the benefits and risks of Cuprior?

Answer

Since Cuprior is a hybrid medicine, its benefits and risks are taken as being the same as the reference medicine's.

Question

Why is Cuprior approved?

Answer

The Agency's Committee for Medicinal Products for Human Use (CHMP) decided that Cuprior's benefits are greater than its risks and recommended that it be approved for use in the EU.

The CHMP noted that trientine has been used for over 30 years to treat patients with Wilson's disease. Although Cuprior releases more trientine in the body than the reference medicine, this difference can be addressed by lowering the dose, which is in any case adjusted according to patient response and levels of copper in the body.

Question

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

Answer

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

Question

Other information about Cuprior

Answer

The European Commission granted a marketing authorisation valid throughout the European Union for Cuprior on 5 September 2017.

For more information about treatment with Cuprior, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Question

What is Cuprior and what is it used for?

Answer

Cuprior is a medicine used to treat patients aged 5 years and older with Wilson's disease, a genetic condition in which copper absorbed from food builds up in the body, particularly in the liver and the brain, causing damage. Cuprior is used in patients who cannot take D-penicillamine, another medicine for this condition.

Cuprior contains the active substance trientine. It is a hybrid medicine. This means that it is similar to a 'reference medicine' (in this case Trientine Dihydrochloride 300 mg capsules) also containing trientine. The difference between Cuprior and the reference medicine is that Cuprior contains another form of trientine (trientine tetrahydrochloride) and does not need to be stored in a refrigerator.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Cuprior - EMA Approval | MedPath