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A Phase 2, Randomized, Double-Blind, Placebo-Controlled Multi-Center Single Dose Study to Evaluate the Safety and Effectiveness of VNX001 Compared to Placebo, and the Individual Components of Lidocaine, and Heparin in Subjects With Interstitial Cystitis/Bladder Pain Syndrome Who Have an Episode of Acute Bladder Pain of Moderate to Severe Intensity; The Engage 2024 Study
Conditions
Interventions
VNX001
Placebo
+2 more
Locations
14
United States
IC Study LLC
Escondido, California, United States
University of California Los Angeles Center for Women's Pelvic Health
Los Angeles, California, United States
The Clark Center for Urogynecology
Newport Beach, California, United States
The Continence Center Medical Group, Inc dba Southern California Continence Center
Newport Beach, California, United States
University of California San Diego Medical Center
San Diego, California, United States
Prestige Medical Group
Tustin, California, United States
Start Date
May 22, 2023
Primary Completion Date
June 1, 2026
Completion Date
June 1, 2026
Last Updated
January 22, 2026
NCT07391306
NCT00389142
NCT05726786
NCT05149573
NCT05279963
NCT00499317
Lead Sponsor
Vaneltix Pharma, Inc.
Collaborators
Data Source & Attribution
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