Spiolto® Respimat® (Tiotropium/Olodaterol) Versus Triple Combination Therapy in Everyday Clinical Treatment Practice for Chronic Obstructive Pulmonary Disease (EVELUT®)
Launched by BOEHRINGER INGELHEIM · May 15, 2019
Trial Information
Current as of June 24, 2025
Completed
Keywords
ClinConnect Summary
COPD patients on LABA/ICS maintenance therapy with dyspnea (mMRC ≥ 1) and other symptoms (CATTM ≥ 10), who are switched to either Spiolto® Respimat® in the new reusable inhaler or any triple therapy (LAMA + LABA + ICS) as an open or fixed combination according to approved SmPCs at baseline at the discretion of their attending physician.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- Patients can be included if all of the following criteria are met:
- • Diagnosis of COPD
- • Symptomatic (with regard to dyspnea (mMRC Dyspnea score ≥1) AND with regard to symptoms (CAT Score ≥10) at the same time)
- • Patients on LABA/ICS maintenance therapy who are switched to Spiolto® Respimat® in the new reusable inhaler or a free/fixed triple combination of LABA + LAMA + ICS at Visit 1 at the discretion of the treating physician.
- • Adults who are contractually capable and mentally able to understand and follow the instructions of the study personnel
- • Male or female
- • Patients aged ≥40 years of age
- • Written informed consent prior to study participation
- • The patient is willing and able to follow the procedures outlined in the protocol
- Exclusion Criteria:
- • Patients with contraindications acc. to SmPC
- • Patients not on LABA/ICS maintenance treatment at visit 1, e.g., mono or dual bronchodilation only, ICS only, or a triple combination of LAMA + LABA + ICS (either as a fixed combination product or as separate components)
- • Lack of informed consent
- • Pregnant and/or lactating females
- • Acute exacerbation of COPD (within 4 weeks prior to Visit 1)
- • Frequently exacerbating patients, i. e. patients with ≥2 moderate exacerbations within the last 12 months or ≥1 exacerbation leading to hospitalization within the last 12 months
- • Acute respiratory failure (pH \<7,35 and/ or respiratory rate \>30/min within 3 months prior to Visit 1)
- • History or current diagnosis of asthma
- • History or current diagnosis of asthma-COPD overlap
- • History or current diagnosis of allergic rhinitis within the last 5 years
- • History or current diagnosis of lung cancer within the last 5 years
- • Participation in a parallel interventional clinical trial
- • mild exacerbation: additional use of short-acting bronchodilators and treated by the patient without consulting a physician
- • moderate exacerbation: treatment includes medical prescription of a systemic corticosteroid and/or antibiotic
- • severe exacerbation: exacerbation leading to hospitalization
About Boehringer Ingelheim
Boehringer Ingelheim is a global, research-driven pharmaceutical company dedicated to improving health and quality of life through innovative therapies. Established in 1885 and headquartered in Ingelheim, Germany, the company focuses on the development of prescription medicines in key therapeutic areas, including respiratory diseases, cardiovascular health, oncology, and immunology. Boehringer Ingelheim is committed to advancing medical science through rigorous clinical trials and collaborative research, striving to bring novel treatments to patients while upholding the highest standards of safety and efficacy. With a strong emphasis on sustainability and corporate responsibility, the company aims to make a meaningful impact on global health challenges.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Stuttgart, , Germany
Darmstadt, , Germany
Bad Wörishofen, , Germany
Berlin, , Germany
Berlin, , Germany
Büchen, , Germany
Duisburg, , Germany
Garmisch Partenkirchen, , Germany
Gelsenkirchen, , Germany
Grafenrheinfeld, , Germany
Halle (Saale), , Germany
Kamp Lintfort, , Germany
Mannheim, , Germany
Münnerstadt, , Germany
Rostock, , Germany
Rüsselsheim, , Germany
Viernheim, , Germany
Weißenburg I Bay, , Germany
Witten, , Germany
Witten, , Germany
Bad Sachsa, , Germany
Bergisch Gladbach, , Germany
Berkatal, , Germany
Berlin, , Germany
Berlin, , Germany
Bonn, , Germany
Breuberg, , Germany
Bruchsal, , Germany
Böhlen B Leipzig, , Germany
Cottbus, , Germany
Deggingen, , Germany
Dortmund, , Germany
Düsseldorf, , Germany
Forchheim , Oberfr, , Germany
Fürstenwalde /Spree, , Germany
Gelsenkirchen, , Germany
Gelsenkirchen, , Germany
Gütersloh, , Germany
Halle (Saale), , Germany
Hamburg, , Germany
Hamburg, , Germany
Heidelberg , Neckar, , Germany
Heilbad Heiligenstadt, , Germany
Ibbenbüren, , Germany
Jerichow, , Germany
Kamen , Westf, , Germany
Koblenz Am Rhein, , Germany
Kronach , Oberfr, , Germany
Köthen (Anhalt), , Germany
Lahnau, , Germany
Leipzig, , Germany
Leipzig, , Germany
Ludwigshafen Am Rhein, , Germany
Ludwigshafen Am Rhein, , Germany
Marburg, , Germany
Menden (Sauerland), , Germany
Mosbach , Baden, , Germany
München, , Germany
Neumarkt I.D.Opf., , Germany
Nürnberg , Mittelfr, , Germany
Nürnberg, , Germany
Oberhausen , Rheinl, , Germany
Potsdam, , Germany
Radebeul, , Germany
Rathenow, , Germany
Schleswig, , Germany
Schweinfurt, , Germany
Seelow, , Germany
Siegen, , Germany
Straubing, , Germany
Strausberg, , Germany
Trier, , Germany
Ulm, Donau, , Germany
Warendorf, , Germany
Wiesbaden, , Germany
Forchheim, Oberfr, , Germany
Heidelberg, Neckar, , Germany
Kamen, Westf, , Germany
Kronach, Oberfr, , Germany
Mosbach, Baden, , Germany
Nürnberg, Mittelfr, , Germany
Oberhausen, Rheinl, , Germany
Patients applied
Trial Officials
Andrea Marseille, 0049613277141881
Study Chair
andrea.marseille@boehringer-ingelheim.com
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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