Patient Guide: Safety and Efficacy Study of VNX001 Compared to Its Individual Components (Lidocaine and Heparin) or Placebo in Subjects With IC/BPS

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 13 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05737121
Status: 🟢 Enrolling Now
Condition: Interstitial Cystitis, Bladder Pain Syndrome
Phase: PHASE2

Where You Can Participate

This study is available at 13 locations across the country.

Top locations include:
  • • Escondido, California
  • • Los Angeles, California
  • • Newport Beach, California
  • • And 10 more locations

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Safety and Efficacy Study of VNX001 Compared to Its Individual Components (Lidocaine and Heparin) or Placebo in Subjects With IC/BPS - Join Clinical Trial NCTNCT05737121

How to Join This Clinical Trial - NCTNCT05737121

Learn how to participate in this PHASE2 trial studying an investigational therapy for Interstitial Cystitis, Bladder Pain Syndrome. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Interstitial Cystitis, Bladder Pain Syndrome. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Interstitial Cystitis, Bladder Pain Syndrome
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05737121 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 13 locations. Find a study site near you:

Clinical Research Site

Escondido, California 92025 - United States

Status: SUSPENDED

Clinical Research Site

Los Angeles, California 90095 - United States

Status: WITHDRAWN

Clinical Research Site

Newport Beach, California 92663 - United States

Status: RECRUITING

Clinical Research Site

Newport Beach, California 92663 - United States

Status: WITHDRAWN

Clinical Research Site

San Diego, California 92103 - United States

Status: RECRUITING

Clinical Research Site

Tustin, California 92780 - United States

Status: RECRUITING

Clinical Research Site

Hialeah, Florida 33012 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33615 - United States

Status: RECRUITING

Clinical Research Site

Cartersville, Georgia 30120 - United States

Status: RECRUITING

Clinical Research Site

Metairie, Louisiana 70001 - United States

Status: RECRUITING

And 3 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Interstitial Cystitis, Bladder Pain Syndrome:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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