Clinical and demOgRaphic Features of Patients With Uncontrolled Severe Asthma in Russia (CORSAR)
Launched by ASTRAZENECA · Jun 17, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The CORSAR trial is a study focused on understanding the characteristics of adults with uncontrolled severe asthma in Russia. Researchers are looking to gather information from about 5,000 patients across 50 outpatient centers in various regions. Participants must be at least 18 years old and have a diagnosis of uncontrolled severe asthma, which means their asthma symptoms are not well managed despite receiving standard treatments. This study is observational, meaning it does not involve any new treatments or changes to how patients are currently cared for; instead, it aims to collect data based on routine medical practices.
To be eligible, patients should have had their asthma diagnosed as uncontrolled for at least a year and must have medical records showing their condition. However, those currently on certain advanced therapies or with other significant lung diseases will not be included. Participants can expect to share their health information through routine check-ups, helping researchers better understand severe asthma and potentially improve future care for others with this condition.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age ≥ 18 years at the time of inclusion;
- • 2. Signed and dated written informed consent in accordance with ICH GCP and local law prior to inclusion in the study;
- • 3. Patients with diagnosis of uncontrolled SA (Asthma Control Questionnaire-5 (ACQ-5) score \> 1,5) established no less than 52 weeks prior to inclusion; Severe asthma is defined as asthma, that is controlled due to treatment with ICS in medium or high doses plus LABA and/or ALP, and/or LAMA, and/or systemic corticosteroids (sCS), and/or immunobiological therapy, while attempts to reduce the volume of therapy lead to a loss of symptom control, or asthma remains uncontrolled despite this treatment. Such therapy should be carried out at least 3 months before inclusion.
- • Uncontrolled asthma is defined as ACQ-5\>1.5.
- • 4. Patients with the availability of at least 52 weeks of follow-up data (prior to inclusion) in the medical records.
- Exclusion Criteria:
- • 1. Patients receiving any biological therapy currently or within 52 weeks prior to inclusion;
- • 2. Presence of chronic obstructive pulmonary disease (COPD) or idiopathic pulmonary fibrosis (ILF) currently or in the anamnesis;
- • 3. The participation in any clinical study currently or within 52 weeks prior to inclusion;
- • 4. An acute or chronic disease that, as deemed by Investigator, limits the ability of patients to participate in this study or could influence the interpretation of the results.
About Astrazeneca
AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Moscow, , Russian Federation
Ekaterinburg, , Russian Federation
Nizhniy Novgorod, , Russian Federation
Saint Petersburg, , Russian Federation
Saratov, , Russian Federation
Kazan, , Russian Federation
Krasnodar, , Russian Federation
Samara, , Russian Federation
Smolensk, , Russian Federation
Stavropol, , Russian Federation
Krasnoyarsk, , Russian Federation
Novosibirsk, , Russian Federation
Tomsk, , Russian Federation
Voronezh, , Russian Federation
Ryazan, , Russian Federation
Barnaul, , Russian Federation
Omsk, , Russian Federation
Nizhny Novgorod, , Russian Federation
Ufa, , Russian Federation
Irkutsk, , Russian Federation
Murmansk, , Russian Federation
Vladivostok, , Russian Federation
Saint Petersburg, , Russian Federation
Chelyabinsk, , Russian Federation
Petrozavodsk, , Russian Federation
Vladimir, , Russian Federation
Bryansk, , Russian Federation
Volgograd, , Russian Federation
Astrakhan, , Russian Federation
Yekaterinburg, , Russian Federation
Khabarovsk, , Russian Federation
Orenburg, , Russian Federation
Blagoveshchensk, , Russian Federation
Ulan Ude, , Russian Federation
Nalchik, , Russian Federation
Ulan Ude, , Russian Federation
Verkhnyaya Pyshma, , Russian Federation
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported