IMA Brasil - Instituto de Pesquisa Clínica e Medicina Avançada
São Paulo, Brazil
NCT Number: NCT01202084
The primary objective will be to compare the impact of the study formulations on pulmonary function in persistent asthma carriers.
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Notify Me12 year and older
All sexes
Interventional
Phase 3
São Paulo, Brazil
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 12 weeks
Time frame: 12 weeks
Eurofarma Laboratorios S.A.
Industry
A Phase III, Randomized, Open-label, Non-inferiority Study Comparative of Formoterol/Fluticasone Eurofarma 12/250 µg, Foraseq® 12/400 µg and Fluticasone 500 µg in Asthma Patients
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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