Basic Information
EMA regulatory identification and product classification information
EMA Identifiers
Overview Summary
Comprehensive product overview and regulatory summary
This is a summary of the European public assessment report (EPAR) for Copalia HCT. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Copalia HCT.
If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis for the CHMP recommendations, read the scientific discussion (also part of the EPAR).
Active Substances (3)
amlodipine
valsartan
hydrochlorothiazide
Documents (17)
Copalia HCT : EPAR - Summary for the public
November 17, 2009
OVERVIEW_DOCUMENT
Copalia HCT-H-C-1160-WS-359 : EPAR - Assessment Report - Variation
December 11, 2013
CHANGES_SINCE_INITIAL_AUTHORISATION
Angiotensin-II-receptor antagonists (sartans) : Scientific conclusions - Impact of the Article 5(3) scientific opinion on nitrosamines
July 5, 2021
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT : EPAR - Procedural steps taken and scientific information after authorisation (archive)
August 25, 2010
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT : EPAR - Public assessment report
November 17, 2009
CHANGES_SINCE_INITIAL_AUTHORISATION
Committee for medicinal products for human use summary of positive opinion for Copalia HCT
July 22, 2009
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT : EPAR - All Authorised presentations
November 17, 2009
AUTHORISED_PRESENTATIONS
Copalia HCT-H-C-1159-A31-30: EPAR - Scientific conclusions, grounds for variation to the terms of the marketing authorisations and detailed explanation of the scientific grounds for the differences from the PRAC recommen...
September 30, 2014
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP post-authorisation summary of positive opinion for Copalia HCT
June 27, 2013
CHANGES_SINCE_INITIAL_AUTHORISATION
Angiotensin-II-receptor antagonists (sartans) Article 31 referral - CHMP assessment report - Impact of the Article 5(3) scientific opinion on nitrosamines
March 2, 2021
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT : EPAR - Product Information
November 16, 2009
DRUG_PRODUCT_INFORMATION
Copalia HCT : EPAR - Scientific conclusions - Annex IV
May 23, 2019
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT-H-C-1159-A31-30 : EPAR - Assessment Report - Article 31
September 30, 2014
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT : EPAR - Public assessment report
November 17, 2009
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Committee for medicinal products for human use summary of positive opinion for Copalia HCT
July 22, 2009
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Angiotensin-II-receptor antagonists (sartans) Article 31 referral - CHMP assessment report
May 2, 2019
CHANGES_SINCE_INITIAL_AUTHORISATION
Copalia HCT : EPAR - Procedural steps taken and scientific information after authorisation
February 12, 2025
CHANGES_SINCE_INITIAL_AUTHORISATION
Overview Q&A (9)
Question
How is Copalia HCT used?
Answer
Copalia HCT is taken by mouth as one tablet once a day, at the same time of the day and preferably in the morning. The dose of Copalia HCT to be used is the same as the doses of three individual active substances that the patient was taking before. The daily dose of Copalia HCT should not exceed 10 mg of amlodipine, 320 mg of valsartan and 25 mg of hydrochlorothiazide.
Question
What is Copalia HCT?
Answer
Copalia HCT is a medicine that contains three active substances, amlodipine, valsartan and hydrochlorothiazide. It is available as tablets containing amlodipine, valsartan and hydrochlorothiazide in the following amounts: 5/160/12.5 mg, 10/160/12.5 mg, 5/160/25 mg; 10/160/25 mg and 10/320/25 mg.
Question
How does Copalia HCT work?
Answer
The three active substances in Copalia HCT are antihypertensive medicines that are already in use in the European Union (EU).
Amlodipine is a ‘calcium-channel blocker’. It blocks special channels on the surface of cells called calcium channels, through which calcium ions normally enter the cells. When calcium ions enter the cells in the muscles of blood-vessel walls, this causes contraction. By reducing the flow of calcium into the cells, amlodipine prevents the cells from contracting and helps the blood-vessel walls to relax and widen, thereby reducing blood pressure.
Valsartan is an ‘angiotensin-II-receptor antagonist’, which means that it blocks the action of a body hormone called angiotensin II. Angiotensin II is a powerful vasoconstrictor (a substance that narrows blood vessels). By blocking the receptors to which angiotensin II normally attaches, valsartan stops the hormone having an effect, allowing the blood vessels to widen and blood pressure to reduce. Hydrochlorothiazide is a diuretic. It works by increasing urine output, reducing the volume of fluid in the blood and lowering the blood pressure.
The combination of the three active substances has an additive effect, reducing the blood pressure more than the individual medicines alone. By lowering the blood pressure, the risks associated with high blood pressure, such as having a stroke, are reduced.
Question
Other information about Copalia HCT
Answer
The European Commission granted a marketing authorisation valid throughout the European Union for Copalia HCT on 4 November 2009.
Question
What benefit has Copalia HCT shown during the studies?
Answer
Treatment with the highest strength of Copalia HCT was more effective at treating hypertension than dual combinations containing any of the two active substances. The average reduction in blood pressure was around 39.7/24.7 mmHg in patients taking Copalia HCT compared with 32/19.7 mmHg, 33.5/21.5 mmHg and 31.5/19.5 mmHg in patients taking valsartan/hydrochlorothiazide, valsartan/amlodipine and hydrochlorothiazide/amlodipine combinations, respectively.
Question
Why has Copalia HCT been approved?
Answer
The CHMP noted that patients already taking the three active substances would be more likely to comply with their treatment if prescribed Copalia HCT which combines the three substances in a single tablet. The main study showed the benefit of the highest strength of Copalia HCT in lowering the blood pressure. For all doses, Copalia HCT also met requirements to prove that it was comparable to the combinations of the individual active substances taken separately. The CHMP therefore decided that Copalia HCT’s benefits are greater than its risks and recommended that it be given marketing authorisation.
Question
What is Copalia HCT used for?
Answer
Copalia HCT is used to treat essential hypertension (high blood pressure) in adults whose blood pressure is already adequately controlled with a combination of amlodipine, valsartan and hydrochlorothiazide. ‘Essential’ means that the hypertension has no obvious cause.
The medicine can only be obtained with a prescription.
Question
How has Copalia HCT been studied?
Answer
Because the combination of the three active substances has been in use for a number of years, the company presented studies showing that the tablet containing all three substances is absorbed in the body in the same way as the separate tablets.
In addition, one main study was carried out in 2,271 patients with moderate to severe hypertension with the highest strength of Copalia HCT (320 mg valsartan, 10 mg amlodipine and 25 mg hydrochlorothiazide). Patients received either Copalia HCT or one of the three combinations containing only two of the active substances for eight weeks. The main measure of effectiveness was the average change in the blood pressure.
Question
What is the risk associated with Copalia HCT?
Answer
The most common side effects with Copalia HCT (seen in between 1 and 10 patients in 100) are hypokalaemia (low blood potassium levels), dizziness, headache, hypotension (low blood pressure), dyspepsia (heartburn), pollakiuria (abnormally frequent urination), fatigue (tiredness) and oedema (fluid retention). For the full list of all side effects reported with Copalia HCT, see the package leaflet.
Copalia HCT must not be used in people who are hypersensitive (allergic) to the active substances, to other sulfonamides, to dihydropyridine derivatives or to any of the other ingredients in Copalia HCT. It must not be used in women who are more than three months pregnant. It must also not be used in patients who have liver or bile problems (such as jaundice), severe kidney problems, anuria (a condition in which a patient cannot make or pass urine) or in patients undergoing dialysis (a blood clearance technique). Finally, Copalia HCT must not be used in patients with hypokalaemia (low blood potassium levels), hyponatraemia (low blood sodium levels) and hypercalcaemia (high blood calcium levels) that do not respond to treatment and in patients with hyperuricaemia (high blood levels of uric acid) that causes symptoms.
Copalia HCT must also not be used in combination with aliskiren-containing medicines (also used to treat essential hypertension) in patients with type 2 diabetes or in patients with moderate or severe kidney impairment.