Viewing Study NCT03320850


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Study NCT ID: NCT03320850
Status: COMPLETED
Last Update Posted: 2021-08-13
First Post: 2017-10-23
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: BOTOX® Intravesical Instillation in Participants With Overactive Bladder and Urinary Incontinence
Sponsor: Allergan
Organization:

Study Overview

Official Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Single-treatment, 2-stage, Dose-finding Study Evaluating the Efficacy and Safety of BOTOX® Intravesical Instillation in Participants With Overactive Bladder and Urinary Incontinence
Status: COMPLETED
Status Verified Date: 2021-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: APOLLO
Brief Summary: This study will evaluate the efficacy and safety of BOTOX® intravesical instillation in participants with overactive bladder and urinary incontinence.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: