Symbicort Rapihaler Therapeutic Equivalence Study
Launched by ASTRAZENECA · Sep 27, 2007
Trial Information
Current as of June 09, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Asthma clinically diagnosed since at least 6 months.
- • Lung function values measured ≥ 50% and ≤ 90% of predicted normal.
- • Patients with reversible airway obstruction Daily use of inhaled steroids (any brand) for \>3 months.
- Exclusion Criteria:
- • Use of oral, rectal or parenteral steroids within 30 days prior to start of study.
- • Respiratory infection affecting the asthma, as judged by the investigator, within 30 days prior to start of randomised treatment.
- • Any significant disease or disorder which, in the opinion of the investigator, may either put the patient at risk because of participation in the study, or may influence the results of the study or the patient's ability to participate in the study.
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
Budapest, , Hungary
Debrecen, , Hungary
Deszk, , Hungary
Pleven, , Bulgaria
Plovdiv, , Bulgaria
Sofia, , Bulgaria
Varna, , Bulgaria
Pardubice, , Czech Republic
Gyor, , Hungary
Lodz, , Poland
Lublin, , Poland
Szczecin, , Poland
Szeged, , Hungary
Hradec Kralove, , Czech Republic
Poznan, , Poland
Bydgoszcz, , Poland
Gyula, , Hungary
Rousse, , Bulgaria
Praha 8, , Czech Republic
Bialystok, , Poland
Krakow, , Poland
Wroclaw, , Poland
Kladno, , Czech Republic
Neratovice, , Czech Republic
Praha 5, , Czech Republic
Rokycany, , Czech Republic
Strakonice, , Czech Republic
Karpacz, , Poland
Turek, , Poland
Szarvas, , Hungary
Törökbálint, , Hungary
Jihlava, , Czech Republic
Cegléd, , Hungary
Skierniewice, , Poland
Balassagyarmat, , Hungary
Chodziez, , Poland
Ostrow Wielkopolski, , Poland
Tarnow, , Poland
Praha 4, , Czech Republic
Kaposvar, , Hungary
Nyíregyháza, , Hungary
Benesov U Prahy, , Czech Republic
Százhalombatta, , Hungary
Litomerice, , Czech Republic
Chrzanow, , Poland
Kutna Hora, , Czech Republic
Bielsko Biala, , Poland
Lomza, , Poland
Kolin, , Czech Republic
Wodzislaw Slaski, , Poland
Patients applied
Trial Officials
Tomas Andersson
Study Director
AstraZeneca
Akos Somoskovi
Principal Investigator
AstraZeneca
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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