Riltrava Aerosphere

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Authorised

This medicine is authorised for use in the European Union

formoterol fumarate dihydrate / glycopyrronium / budesonide
MedicineHumanAuthorised

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

Riltrava Aerosphere is a medicine used to treat patients with obstructive pulmonary disease (COPD) and asthma.

COPD is a long-term disease in which the airways and air sacs in the lungs become damaged or blocked, leading to difficulty breathing. Riltrava Aerosphere is used for maintenance (regular) treatment of adults with moderate to severe COPD whose disease is not controlled well enough with a combination of inhaled medicines consisting of a long-acting beta-2 agonist plus either a corticosteroid or a long-acting muscarinic antagonist.

Riltrava Aerosphere is also used in patients aged 12 years and older to treat asthma that is not controlled well enough by inhaled medicines combining corticosteroids and a long-acting beta-2 agonist.

Riltrava Aerosphere contains the active substances formoterol, glycopyrronium bromide and budesonide.

This medicine is the same as Trixeo Aerosphere, which is already authorised in the EU. The company that makes Trixeo Aerosphere has agreed that its scientific data can be used for Riltrava Aerosphere (informed consent).

Riltrava Aerosphere can only be obtained with a prescription. It is available as a portable inhaler device. The recommended dose is two inhalations twice a day (two in the morning and two in the evening). Patients should be shown how to use the inhaler correctly by a doctor or other healthcare professional.

For more information about using Riltrava Aerosphere, see the package leaflet or contact your doctor or pharmacist.

Riltrava Aerosphere contains three active substances, which work in different ways to widen the airways and improve breathing in COPD and asthma.

Formoterol is a long-acting beta-2 agonist. It attaches to receptors (targets) known as beta-2 receptors in the muscles of the airways. When it attaches to these receptors, it causes the muscles to relax, which keeps the airways open and helps with the patient’s breathing.

Glycopyrronium bromide is a long-acting muscarinic receptor antagonist. This means that it blocks muscarinic receptors in muscle cells in the airways. Because these receptors help control the contraction of muscles, glycopyrronium causes the muscles of the airways to relax, helping to keep the airways open.

Budesonide belongs to a group of anti-inflammatory medicines known as corticosteroids. It works in a similar way to naturally occurring corticosteroid hormones, reducing the activity of the immune system (the body’s natural defences) by attaching to receptors in various types of immune cells. This leads to a reduction in the release of substances that are involved in the inflammation process, such as histamine, thereby keeping the airways clear and allowing the patient to breathe more easily.

COPD

Two main studies involving over 10,000 patients with moderate to very severe COPD have shown that Riltrava Aerosphere is effective at improving patients’ FEV1 (the maximum volume of air they can breathe out in one second) and at reducing the number of exacerbations (flare-ups) of the disease.

In the first study, patients treated with Riltrava Aerosphere for 24 weeks had FEV1 increases of around 147 ml, compared with 125 ml for patients treated with glycopyrronium and formoterol, and 73 ml and 88 ml for patients treated with two different inhalers containing budesonide and formoterol.

The second study, which lasted one year, showed that patients treated with Riltrava Aerosphere had fewer COPD exacerbations (1.08 per year) than patients treated with glycopyrronium and formoterol (1.42) or budesonide and formoterol (1.24).

Asthma

Riltrava Aerosphere was investigated in two main studies involving more than 4,000 patients with asthma that was not controlled well enough by treatment combining corticosteroids and a long-acting beta-2 agonist. The studies showed that Riltrava Aerosphere improved patients’ breathing and reduced the number of asthma flare ups.

In the first study, after 24 weeks of treatment, FEV1 was 56 ml higher on average in patients given Riltrava Aerosphere than in those given budesonide and formoterol. In the second study, FEV1 was 97 ml higher on average with Riltrava Aerosphere than with budesonide and formoterol. Looking at results from both studies together, severe asthma flare-ups occurred around 15% less often in patients treated with Riltrava Aerosphere than in those treated with budesonide and formoterol.

Studies carried out with Riltrava Aerosphere are described in more detail in the medicine’s assessment reports.

For the full list of side effects and restrictions of Riltrava Aerosphere, see the package leaflet.

When used for COPD, the most common side effects with Riltrava Aerosphere (which may affect up to 1 in 10 people) include pneumonia (lung infection), headache, oral candidiasis (thrush, a fungal infection) and urinary tract infection (infection of the parts of the body that collect and pass out urine).

When used for asthma, the most common side effects (which may affect up to 1 in 10 people) include headache, dysphonia (changes in the sound or tone of the voice) and urinary tract infection.

Riltrava Aerosphere improved lung function and reduced disease flare ups in adults with moderate to severe COPD and people aged 12 years and older with asthma which was not controlled well enough by standard treatments.

The safety of Riltrava Aerosphere is similar to that of medicines containing combinations of a corticosteroid, beta-2 agonist and an antimuscarinic medicine.

The European Medicines Agency therefore decided that Riltrava Aerosphere’s benefits are greater than its risks and it can be authorised for use in the EU.

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

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

Riltrava Aerosphere received a marketing authorisation valid throughout the EU on 6 January 2022.

For information about the availability of this medicine in your country, contact your national competent authority.

This overview was last updated in 08-2026.

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Latest procedure affecting product information:X/0000287672
18/09/2026
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This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

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Product details

Name of medicine
Riltrava Aerosphere
Active substance
  • Budesonide
  • formoterol fumarate dihydrate
  • glycopyrronium bromide
International non-proprietary name (INN) or common name
  • formoterol fumarate dihydrate
  • glycopyrronium
  • budesonide
Therapeutic area (MeSH)
Pulmonary Disease, Chronic Obstructive
Anatomical therapeutic chemical (ATC) code
R03AL11

Pharmacotherapeutic group

Drugs for obstructive airway diseases

Therapeutic indication

Riltrava Aerosphere is indicated as a maintenance treatment of asthma in patients 12 years of age and older who are not adequately controlled by a combination of a medium dose inhaled corticosteroid and a long acting beta2 agonist.

Riltrava Aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (COPD) who are not adequately treated by a combination of an inhaled corticosteroid and a long acting beta2 agonist or combination of a long-acting beta2 agonist and a long acting muscarinic antagonist. 

Authorisation details

EMA product number
EMEA/H/C/005311
Marketing authorisation holder
AstraZeneca AB

SE-151 85 Sodertalje
Sweden

Opinion adopted
11/11/2021
Marketing authorisation issued
06/01/2022
Revision
7

Assessment history

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