MedPath

Study of OnabotulinumtoxinA (BOTOX®) for Urinary Incontinence Due to Neurogenic Detrusor Overactivity in Pediatric Patients

Phase 3
Completed
Conditions
Urinary Incontinence
Interventions
Biological: OnabotulinumtoxinA
Registration Number
NCT01852045
Lead Sponsor
Allergan
Brief Summary

This study will evaluate the 3 doses of onabotulinumtoxinA (botulinum toxin Type A) for the treatment of urinary incontinence due to neurogenic detrusor overactivity in pediatric participants between the ages of 5 to 17 years to determine if 1 or more doses were safe and effective.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
114
Inclusion Criteria
  • Urinary incontinence due to neurogenic detrusor overactivity
  • Regularly using clean intermittent catheterization to empty the bladder
Read More
Exclusion Criteria
  • Surgery of the spinal cord within 6 months
  • Diagnosis of cerebral palsy
  • Current or planned use of a baclofen pump
  • Current or planned use of an electrostimulation/neuromodulation device for urinary incontinence
  • Use of an indwelling catheter for urinary incontinence instead of using clean intermittent catheterization to empty the bladder
  • Previous or current use of botulinum toxin therapy of any serotype for any urological condition, or treatment with botulinum toxin of any serotype within 3 months for any other condition or use
  • Myasthenia gravis, Eaton-Lambert syndrome, or amyotrophic lateral sclerosis
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
OnabotulinumtoxinA 200 UOnabotulinumtoxinAOnabotulinumtoxinA (botulinum toxin Type A) 200 U (not to exceed 6 U/kg) injected into the detrusor wall on Day 1. Participants were eligible for retreatment in study 191622-121 if qualified.
OnabotulinumtoxinA 50 UOnabotulinumtoxinAOnabotulinumtoxinA (botulinum toxin Type A) 50 U (not to exceed 6 U/kg) injected into the detrusor wall on Day 1. Participants were eligible for retreatment in study 191622-121 (NCT01852058) if qualified.
OnabotulinumtoxinA 100 UOnabotulinumtoxinAOnabotulinumtoxinA (botulinum toxin Type A) 100 U (not to exceed 6 U/kg) injected into the detrusor wall on Day 1. Participants were eligible for retreatment in study 191622-121 if qualified.
Primary Outcome Measures
NameTimeMethod
Change From Baseline in Daily Average Frequency of Daytime Urinary Incontinence EpisodesBaseline (Day -28 to Day -1) to 2 consecutive days prior to Week 6

Urinary incontinence was defined as involuntary loss of urine as recorded by the participant in a bladder diary during the 2 consecutive days (normalized to a 12-hour daytime period) prior to the study visit. Daytime was defined as the time between waking up to start the day and first morning catheterization and going to bed to sleep for the night. The number of incontinence episodes were averaged daily during this period. A negative change from Baseline indicates improvement. Least squares estimates were based on an Analysis of Covariance (ANCOVA) model.

Secondary Outcome Measures
NameTimeMethod
Number of Participants With Treatment Emergent Adverse Events (TEAE)First study treatment to 12 weeks after last treatment (Up to 48 weeks after first study injection)

An adverse event is any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment. An adverse event can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product. A TEAE is defined as any new adverse event or worsening of an existing condition after initiation of treatment.

Change From Baseline in Average Urine Volume at First Morning CatheterizationBaseline (Day -28 to Day -1) to 2 consecutive days prior to Week 6

The change in urine volume at first morning catherization was recorded by the participant in a bladder diary in the 2 consecutive days during the week prior to the study visit. A positive change from Baseline indicates improvement. Least squares estimates were based on an ANCOVA model.

Time to Participant Request for Retreatment48 weeks

Time from treatment on Day 1 to request for retreatment was estimated. For those participants who did not request retreatment, their data was censored using the date of their last study visit.

Percentage of Participants With Night Time Urinary IncontinenceBaseline (Day -28 to Day -1), Week 6

Urinary incontinence was defined as involuntary loss of urine and the presence or absence of night time urinary incontinence was recorded by the participant in a bladder diary in the 2 consecutive days (normalized to a 12-hour daytime period) during the week prior to the study visit. Night time was defined as the time between going to bed to sleep for the night and waking up to start the day. The percentage of participants with night time urinary incontinence is presented in categories (0, 1, 2 nights).

Change From Baseline in Maximum Detrusor Pressure (PdetMax) During the Storage PhaseBaseline (Day 1) to Week 6

Urodynamic tests were performed by site personnel qualified for performing pressure/flow cystometry. The results were verified by an independent central reviewer. Cystometry was used to measures the pressure inside of the bladder to see how well the bladder was working. A negative change from Baseline indicates improvement. Least squares estimates were based on an ANCOVA model.

Change From Baseline in Detrusor Leak Point Pressure (DLPP) During the Storage PhaseBaseline (Day -28 to -1) to Week 6

DLPP was defined as the lowest detrusor pressure at which urine leakage occurs in the absence of either a detrusor contraction or increased intra-abdominal pressure. Urodynamic tests were performed by site personnel qualified for performing pressure/flow cystometry. The results were verified by an independent central reviewer. Cystometry was used to measures the pressure inside of the bladder to see how well the bladder was working. A negative change from Baseline indicates improvement. Least squares estimates are based on an ANCOVA model.

Change From Baseline in Maximum Cystometric Capacity (MCC)Baseline (Day -28 to Day -1) to Week 6

The MCC was defined by urodynamics, as the volume infused before the participant felt they could no longer delay micturition (has a strong desire to void), had a leakage, or 500 mL was instilled. A positive change from Baseline indicates improvement (increase) in the maximum volume of urine the bladder holds. Least squares estimates were based on an ANCOVA model.

Percentage of Participants With Involuntary Detrusor Contractions (IDC)Baseline (Day -28 to -1) and Week 6

Urodynamic tests were performed by site personnel qualified for performing pressure/flow cystometry. The results were verified by an independent central reviewer. Cystometry was used to measures the presence of involuntary detrusor contractions upon filling. A reduction in IDCs from Baseline to Week 6 indicates improvement.

Change From Baseline in Maximum Detrusor Pressure During the First IDC (PdetMax1stIDC) in Participants With IDCBaseline (Day-28 to Day-1) to Week 6

Urodynamic tests were performed by site personnel qualified for performing pressure/flow cystometry. The results were verified by an independent central reviewer. Cystometry was used to measures the pressure inside of the bladder to see how well the bladder was working. A negative change from Baseline indicates improvement. Least squares estimates were based on an ANCOVA model.

Time to Participant Qualification for Retreatment48 weeks

In order to qualify for retreatment, the criteria listed below must be fulfilled at the qualification for retreatment visit: Participant/parent/caregiver requests retreatment, participant has a total of at least 2 daytime urinary incontinence episodes over the 2-day bladder diary collection period, at least 12 weeks has elapsed since treatment 1 and participant has not experienced a serious treatment-related adverse event at any time.

Trial Locations

Locations (31)

Ann & Robert H. Lurie Children's Hospital of Chicago

🇺🇸

Chicago, Illinois, United States

Cedars-Sinai Medical Center

🇺🇸

Los Angeles, California, United States

Riley Hospital for Children

🇺🇸

Indianapolis, Indiana, United States

Washington University School of Medicine

🇺🇸

Saint Louis, Missouri, United States

Pediatric Urology Associates, PC

🇺🇸

Tarrytown, New York, United States

McKay Urology Carolinas Medical Center

🇺🇸

Charlotte, North Carolina, United States

McMaster University Medical Centre

🇨🇦

Hamilton, Ontario, Canada

Fakultni nemocnice Hradec Kralove

🇨🇿

Hradec Králové, Czechia

Hopital Pellegrin - Enfants

🇫🇷

Bordeaux, France

CHU de Limoges - Hopital Mere et l'Enfant

🇫🇷

Limoges, France

Fakultni nemocnice Olomouc

🇨🇿

Olomouc, Czechia

Hopital Trousseau

🇫🇷

Paris, France

Seconda Università di Napoli

🇮🇹

Caserta, Italy

Necker Enfants Malades Hospital

🇫🇷

Paris, France

William Beaumont Hospital Research Institute

🇺🇸

Royal Oak, Michigan, United States

Copernicus Podmiot Leczniczy Sp. z o. o., Kliniczny Oddzial Chirurgii i Urologii Dzieci i Mlodziezy GUMed

🇵🇱

Gdansk, Poland

Samodzielny Publiczny Szpital Kliniczny Nr 1 we Wroclawiu

🇵🇱

Wroclaw, Poland

Ankara University Medical Faculty Cebeci Hospital

🇹🇷

Ankara, Turkey

Children's Hospital of Orange County

🇺🇸

Orange, California, United States

UZ Leuven

🇧🇪

Leuven, Belgium

Specjalistyczny Gabinet Lekarski

🇵🇱

Poznan, Poland

UZ Antwerpen

🇧🇪

Antwerpen, Belgium

CHU Sainte-Justine

🇨🇦

Montreal, Quebec, Canada

IRCCS Ospedale Pediatrico Bambino Gesu

🇮🇹

Roma, Italy

UZ Gent , Urology

🇧🇪

Gent, Belgium

University of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

Duke University Health System

🇺🇸

Durham, North Carolina, United States

Cincinnati Children's Hospital Medical Center

🇺🇸

Cincinnati, Ohio, United States

Oklahoma Childrens Hospital

🇺🇸

Oklahoma City, Oklahoma, United States

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

Children's Hospital of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

© Copyright 2025. All Rights Reserved by MedPath