YM178
DrugOral
NCT Number: NCT00527033
Examine which dose of YM178 is the best in terms of efficacy, safety and tolerability compared to placebo
Looking for future studies?
Notify Me20 year–80 year
All sexes
Interventional
Phase 2
Chūbu, Japan
To investigate the dose-response relationship of YM178 in terms of efficacy, safety and tolerability, and also the superiority of YM178 over placebo.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Oral
Oral
Time frame: 12 weeks
Time frame: 12 weeks
Astellas Pharma Inc
Industry
A Randomized, Double-blind, Parallel-group, Placebo-controlled Study in Patients With Symptomatic Overactive Bladder
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.
Published trials that share one or more normalized conditions with this study.
NCT05880862
Accidental Falls, Female Urogenital Diseases
Galveston, Texas, United States
View Trial DetailsNCT03784170
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
Woodbury, Minnesota, United States
View Trial DetailsNCT03681678
Burning Vagina, Dyspareunia
Royal Oak, Michigan, United States
View Trial DetailsNCT01558856
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
Montpellier, France
View Trial Details