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Generated: December 11, 2018

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CLINICAL TRIALS PROFILE FOR OLODATEROL HYDROCHLORIDE

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Clinical Trials for Olodaterol Hydrochloride

Trial ID Title Status Sponsor Phase Summary
NCT01153711 Relative Bioavailability of of Olodaterol and Ketoconazole Completed Boehringer Ingelheim Phase 1 This clinical trial is intended to investigate a possible effect of the p-gp inhibitor ketoconazole on the bioavailability of olodaterol
NCT01153724 Relative Bioavailability of Olodaterol and Fluconazole Completed Boehringer Ingelheim Phase 1 This clinical trial is intended to investigate a possible effect of the CYP 2C9 inhibitor fluconazole on the bioavailability of olodaterol
NCT01311661 A Study to Compare the Efficacy and Safety of Different Dosings of Olodaterol Administered With the Respimat® Inhaler in Patients With Moderate to Severe Asthma Completed Boehringer Ingelheim Phase 2 This study will compare efficacy and safety of different regimens of olodaterol administration in asthma (once daily, twice daily) with placebo in a complete cross-over design each within one of the two daily dose groups (medium or high daily dose).
NCT01428622 Olodaterol Bridging Study in Asthma Withdrawn Boehringer Ingelheim Phase 2 The aim of the study is to establish the olodaterol dose in the ethanolic fixed dose combination (FDC) with BI 54903 which is equivalent in bronchodilator effect and systemic exposure to the 5 µg olodaterol reference dose in the aqueous inhalation solution (AIS).
NCT01431274 Tiotropium+Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD) Completed Boehringer Ingelheim Phase 3 The overall objective of this study is to assess the efficacy and safety of 52 weeks once daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the RESPIMAT Inhaler) compared with the individual components ( tiotropium, olodaterol) (delivered by the RESPIMAT Inhaler) in patients with Chronic Obstructive Pulmonary Disease (COPD).
NCT01431287 Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD) Completed Boehringer Ingelheim Phase 3 The overall objective of this study is to assess the efficacy and safety of 52 weeks once daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the RESPIMAT Inhaler) compared with the individual components (tiotropium, olodaterol) (delivered by the RESPIMAT Inhaler) in patients with COPD.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Olodaterol Hydrochloride

Condition Name

Condition Name for Olodaterol Hydrochloride
Intervention Trials
Pulmonary Disease, Chronic Obstructive 29
Asthma 3
Chronic Obstructive Pulmonary Disease 2
Healthy 2
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Condition MeSH

Condition MeSH for Olodaterol Hydrochloride
Intervention Trials
Pulmonary Disease, Chronic Obstructive 31
Lung Diseases 31
Chronic Disease 29
Lung Diseases, Obstructive 11
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Clinical Trial Locations for Olodaterol Hydrochloride

Trials by Country

Trials by Country for Olodaterol Hydrochloride
Location Trials
United States 235
Canada 44
Germany 22
Australia 14
United Kingdom 13
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Trials by US State

Trials by US State for Olodaterol Hydrochloride
Location Trials
South Carolina 14
Virginia 11
North Carolina 11
Missouri 10
California 9
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Clinical Trial Progress for Olodaterol Hydrochloride

Clinical Trial Phase

Clinical Trial Phase for Olodaterol Hydrochloride
Clinical Trial Phase Trials
Phase 4 9
Phase 3 15
Phase 2 4
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Clinical Trial Status

Clinical Trial Status for Olodaterol Hydrochloride
Clinical Trial Phase Trials
Completed 19
Recruiting 8
Not yet recruiting 4
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Clinical Trial Sponsors for Olodaterol Hydrochloride

Sponsor Name

Sponsor Name for Olodaterol Hydrochloride
Sponsor Trials
Boehringer Ingelheim 32
University of Dundee 2
Queen's University 1
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Sponsor Type

Sponsor Type for Olodaterol Hydrochloride
Sponsor Trials
Industry 33
Other 5
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