Evaluate the Safety and Efficacy of Botulax® Versus Botox® in Patient With Overactive Bladder

NCT ID: NCT04186442

Last Updated: 2022-04-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 38 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-05-12
• Study Completion Date: 2021-10-26

Brief Summary

To determine the efficacy and safety of Botulax® in treatment of Overactive Bladder

Detailed Description

A Multicenter, Double-blind, Randomized, Parallel, Active-controlled, Phase I Clinical Trial to Compare the Safety and Efficacy of Botulax® versus Botox® in Patient with Overactive Bladder

Conditions

Overactive Bladder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Botulinum toxin type A (Botulax®)

Group Type: EXPERIMENTAL

Botulinum toxin type A injection

Intervention Type: DRUG

Experimental

Botulinum toxin type A (Botox®)

Group Type: ACTIVE_COMPARATOR

Botulinum Toxin Type A Injection [Botox]

Intervention Type: DRUG

Active Comparator

Interventions

Botulinum toxin type A injection

Experimental

Intervention Type: DRUG

Botulinum Toxin Type A Injection [Botox]

Active Comparator

Intervention Type: DRUG

Other Intervention Names

Botulax®; Botox®

Eligibility Criteria

Inclusion Criteria

1. Female at the age of 19 or older

2. Subjects who agree to participate in the clinical study and voluntarily sign the written informed consent form

3. Subjects with idiopathic overactive bladder who meets the following conditions:

1. Subjects with persistent overactive bladder symptoms for the last 12 weeks

2. Subjects who are not properly controlled by the administration of anticholinergic agents for 4 weeks or more or who are difficult to treat due to adverse reactions

3. Subjects with urinary incontinence, urgency, and urinary frequency symptoms

4. Subjects who are willing to perform clean intermittent catheterization (CIC), if needed

Exclusion Criteria

Subjects who are eligible for any of the following conditions may not participate in this study:

1. Subjects with the following comorbidities:

1. Subjects with peripheral motor neuron disease (eg. amyotrophic lateral sclerosis, motor neuropathy) or systemic neuromuscular junction disorders (eg. myasthenia gravis, Lambert-Eaton syndrome)

2. Overactive bladder patients due to neurological factors (eg stroke, spinal cord disease, Parkinson's disease, etc.)

3. Subjects with clinically significant stress incontinence

4. Subjects with Urinary Tract Infections*

• Culture showing ≥10^5 colony-forming units (CFU)/mL and leukocytes ≥5 high power field (HPF)

5. Patients with acute urinary retention, or with a history or accompanying diseases that can cause urinary retention (urolithiasis, acute cystitis, foreign body in the bladder, bladder flow, etc.)

6. Uncontrolled diabetes patients who meet one or more of the following criteria:

• HbA1c ≥ 9% at screening
• Patients with over 10 years of diabetes
• Have diabetic chronic complications (eg diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, etc.)
• Patients taking a drug that causes glycosuria (sodium-glucose co-transporter 2 inhibitor, SGLT2 inhibitor)

2. Those who have had lower urinary tract surgery within 24 weeks before screening

3. Those who received botulinum toxin due to urinary system disease within 24 weeks before screening

4. Those who have been administered botulinum toxin type A within 12 weeks prior to screening or botulinum toxin type B within 16 weeks of treatment, or planned during the clinical trials

5. Those who have received or plan to receive oral medications for overactive bladder including anticholinergic drugs within 1 week prior to randomization

6. Those who received antiplatelet and anticoagulants within 1 week prior to randomization

7. Subjects with a history of hypersensitivity reactions to any of the components of the investigational product

8. Women of childbearing potential who are planning to become pregnant during the clinical trials or are not using an appropriate method of contraception

9. Those who participated in another clinical trial within 12 weeks prior to screening and received investigational product/medical device/medical procedure

10. Those who are sensitive to cephalosporin or penicillin antibiotics

• Minimum Eligible Age: 19 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Hugel

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Hugel

Seoul, Korea, South Korea

Countries

South Korea

Other Identifiers

HG-BOTOAB-PI-01

Identifier Type: -

Identifier Source: org_study_id