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A Multicentre, Open-Label, Single Dose, Phase 1 Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Mirabegron Oral Suspension in Pediatric Subjects From 3 to Less Than 12 Years of Age With Neurogenic Detrusor Overactivity (NDO) or Overactive Bladder (OAB)
Conditions
Interventions
mirabegron
Locations
3
Denmark
Site DK45002
Aalborg, Denmark
Site DK45001
Aarhus, Denmark
Site PL48001
Warsaw, Poland
Start Date
December 17, 2015
Primary Completion Date
September 30, 2016
Completion Date
September 30, 2016
Last Updated
October 31, 2024
NCT06789406
NCT05362292
NCT07193407
NCT07195656
NCT07209397
NCT03952299
Lead Sponsor
Astellas Pharma Europe B.V.
Data Source & Attribution
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