Study Details
A Study With Mirabegron 50 mg and 25 mg in Chinese Participants with Overactive Bladder
Clinicaltrials.gov ID
Astellas Study ID
178-MA-2295
EudraCT ID
N/A
Condition
Urge to Urinate, Overactive Bladder Disease
Phase
Phase 4
Age
18 Years - N/A
Sex
Female & Male
Product
mirabegron
Type
Interventional
Trial Dates
Jan 2021 - Mar 2022
Masking
None (Open Label)
Enrollment number
249
A Phase 4, Open-label, Randomized, Prospective, Interventional Post-authorization Efficacy and Safety Study of Mirabegron 50 mg and 25 mg for the Treatment of Overactive Bladder in Chinese Subjects
Study summary
Study documents
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Locations
Site CN86001
Beijing, China
Site CN86020
Wuhan, China
Site CN86022
Wuxi, China
Site CN86013
Shanghai, China
Site CN86003
Lanzhou, China
Site CN86009
Guangzhou, China
Site CN86004
Beijing, China
Site CN86011
Wuhan, China
Site CN86010
Chengdu, China
Site CN86007
Zhengzhou, China
Site CN86014
Beijing, China
Site CN86012
Xi'an, China
Site CN86002
Suzhou, China
Site CN86018
Guangzhou, China
Site CN86021
Taiyuan, China