Engage 24: Evaluation of the Safety and Effectiveness of URG101 in Subjects With Interstitial Cystitis/Bladder Pain Syndrome
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|ClinicalTrials.gov Identifier: NCT02591199|
Recruitment Status : Terminated (Prematurely terminated based on interim study analysis)
First Posted : October 29, 2015
Last Update Posted : July 11, 2018
|Condition or disease||Intervention/treatment||Phase|
|Interstitial Cystitis Bladder Pain Syndrome||Drug: URG101 Drug: Placebo Drug: Lidocaine Drug: Heparin||Phase 2|
This is a Phase 2a, randomized, double-blind, placebo controlled, multicenter, single-dose, pharmacokinetic study designed to determine the efficacy and safety of the combination product (URG101) compared with its individual components (Heparin Sodium and Lidocaine Hydrochloride).
Eligible subjects exhibiting moderate to severe symptoms of bladder pain associated with their diagnosis of interstitial cystitis/bladder pain syndrome who have signed informed consent, will be screened and provisionally enrolled for intravesical treatment.
On the day of study drug administration subjects will be randomized (2:1:2:1; URG101:placebo:lidocaine:heparin) and will receive a single administration of one of four intravesical treatments in a blinded fashion, based on random assignment:
- URG101 (buffered lidocaine-heparin)
- Placebo (phosphate buffer)
- Lidocaine hydrocholoride buffered alone
- Heparin sodium buffered alone
Efficacy and safety assessments will be completed for 24 hours after study drug administration. End of Study Follow-up will be completed by telephone 48 to 72 hours after study drug administration.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||92 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Multi-Center Single Dose Study to Evaluate the Safety and Effectiveness of URG101 Compared With the Individual Components Lidocaine and Heparin in Subjects With Interstitial Cystitis/Bladder Pain Syndrome|
|Study Start Date :||September 2015|
|Actual Primary Completion Date :||May 14, 2018|
|Actual Study Completion Date :||June 18, 2018|
A single 15 mL dose of URG101,a mix of buffered Lidocaine (200 mg) and Heparin (50,000 IU), delivered to the bladder via catheter.
Placebo Comparator: Placebo
A single 15 mL dose of placebo delivered to the bladder via catheter.
A single 15 mL dose of buffered Lidocaine (200 mg) delivered to the bladder via catheter.
A single 15 mL dose of buffered Heparin (50,000 IU) delivered to the bladder.
- Change in bladder pain differences from baseline as determined by using the Visual Analog Scale (VAS) [ Time Frame: 24 hours ]The primary objective is to evaluate the change in bladder pain intensity differences from baseline to either 12 hours or 24 hours after administration of URG101 compared with the administration of lidocaine alone, heparin alone, and placebo as determined by using the Visual Analog Scale (VAS).
- Change in urgency from baseline as determined using the VAS [ Time Frame: 24 hours ]Evaluate the change in urgency intensity differences from baseline to 12 or 24 hours after administration of URG101 compared to lidocaine alone, heparin alone, and placebo using the VAS.
- The relationship of plasma lidocaine concentrations at 1 hour after study drug administration to bladder pain and urgency [ Time Frame: 24 hours ]Evaluate the relationship of plasma lidocaine concentrations at 1 hour after study drug administration to bladder pain and urgency at 1 hour, and from baseline to 12 and 24 hours after treatment with URG101 compared to lidocaine alone, heparin alone, and placebo.
- Safety and tolerability of study medication (Adverse events) [ Time Frame: Up to 72 hours ]Adverse events reported after treatment with URG101 compared to lidocaine alone, heparin alone, and placebo.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02591199
|United States, California|
|IC Study, LLC|
|Escondido, California, United States, 92025|
|University of California San Diego|
|San Diego, California, United States, 92103|
|United States, Georgia|
|Cartersville, Georgia, United States, 30120|
|United States, Kansas|
|The Urogynecology Center|
|Overland Park, Kansas, United States, 66209|
|United States, New Jersey|
|Rutgers Women's Health Clinic|
|New Brunswick, New Jersey, United States, 08901|
|United States, New York|
|The Arthur Smith Institue for Urology- North Shore Long Island Jewish Health System|
|Lake Success, New York, United States, 11042|
|United States, North Carolina|
|Wake Forest University Health Sciences|
|Winston-Salem, North Carolina, United States, 27103|
|United States, Ohio|
|MetroHealth System, Center for Advanced Gynecology|
|Cleveland, Ohio, United States, 44109|
|United States, South Carolina|
|Medical University of South Carolina|
|Charleston, South Carolina, United States, 29425|
|United States, South Dakota|
|Sioux Falls, South Dakota, United States, 57105|
|United States, Virginia|
|Urology of Virginia, PLLC|
|Virginia Beach, Virginia, United States, 23462|
|Study Chair:||C. Lowell Parsons, MD||Urigen|