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A Two Part, Randomized, Open-label, Cross Over Study in Healthy Elderly Participants to Evaluate the Relative Bioavailability of Hydrobromide Salt Tablet Formulations of Danirixin in the Fed and Fasted States, and to Evaluate the Effect of Food and Gastric Acid Secretion Suppression on Danirixin Pharmacokinetics Following Administration of Hydrobromide Salt Tablets
Conditions
Interventions
Danirixin
Omeprazole
Locations
1
United States
GSK Investigational Site
Overland Park, Kansas, United States
Start Date
March 7, 2018
Primary Completion Date
July 25, 2018
Completion Date
July 25, 2018
Last Updated
May 19, 2021
NCT06831994
NCT02755974
NCT05050591
NCT05913765
NCT05592847
NCT00683722
Lead Sponsor
GlaxoSmithKline
Data Source & Attribution
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