Open-label Long-term Extension Study of Fesoterodine in Japanese Subjects With Neurogenic Detrusor Overactivity.

PHASE3CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

June 5, 2015

Primary Completion Date

April 1, 2020

Study Completion Date

April 1, 2020

Conditions
Urinary Bladder, Neurogenic
Interventions
DRUG

Fesoterodine PR 4 mg

Fesoterodine 4 mg tablet once daily for 28 or 40 weeks

DRUG

Fesoterodine PR 8 mg

Fesoterodine PR 8 mg tablet once daily for 28 or 40 weeks

DRUG

Fesoterodine BIC 2 mg

Fesoterodine BIC 2 mg tablet once daily for 28 weeks

DRUG

Fesoterodine BIC 4 mg

Fesoterodine BIC 4 mg tablet once daily for 28 weeks

Trial Locations (7)

474-8710

Aichi Children's Health and Medical Center, Ōbu

266-0007

Chiba Children's Hospital, Midori-ku Chiba-shi

813-0017

Fukuoka Children's Hospital, Fukuoka

232-8555

Kanagawa Children's Medical Center, Yokohama

594-1101

Osaka Women's and Children's Hospital, Izumi-shi

420-8660

Shizuoka Children's Hospital, Aoi-ku Shizuoka-shi

321-0293

Dokkyo Medical University Hospital, Shimotsuga-gun

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY