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Study identifier: NCT05491525 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Open-label, Long-term Safety, Efficacy, and Pharmacokinetics Study of Vibegron in Pediatric Subjects 2 Years to < 18 Years of Age With NDO and on CIC

Condition: Neurogenic Detrusor Overactivity  ·  Sponsor: Urovant Sciences GmbH

PhasePhase 2/Phase 3
Planned participants71
Who can joinAll sexes, 2 Years to 17 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the safety, efficacy, and PK of Vibegron in pediatric participants with NDO who are regularly using CIC

This description comes directly from the study's public registry record.

Talk to the study team

Study Director  ·  833-876-8268  ·  clinicaltrials@us.sumitomo-pharma.com

Always discuss trial participation with your own doctor first.

Locations (38)

Arkansas Childrens HospitalLittle Rock, Arkansas, United StatesRecruiting
Children's Hospital of Orange CountyOrange, California, United StatesTerminated
Children's Hospital ColoradoAurora, Colorado, United StatesRecruiting
Nemours Childrens Health, JacksonvilleJacksonville, Florida, United StatesRecruiting
Wichita Urology GroupWichita, Kansas, United StatesRecruiting
Childrens Hospital New OrleansNew Orleans, Louisiana, United StatesWithdrawn
Albany Medical CollegeAlbany, New York, United StatesRecruiting
SUNY Upstate Medical UniversitySyracuse, New York, United StatesRecruiting
Duke University Medical CenterDurham, North Carolina, United StatesTerminated
University of OklahomaOklahoma City, Oklahoma, United StatesRecruiting
Oregon Health & Science UniversityPortland, Oregon, United StatesWithdrawn
Universitair Ziekenhuis AntwerpenEdegem, Antwerpen, BelgiumWithdrawn

+ 26 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05491525