Clinical trial
A Phase 2b, Open Label, Single-Arm, Multi-Center, Multiple Dose, 14-Day Study to Evaluate the Safety, Efficacy, and Frequency of Intravesical Administration of VNX001 in Acute Treatment of Subjects With Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) Who Have an Episode of Acute Bladder Pain of Moderate to Severe Intensity
NCT06394830 is registered in ClinicalTrials.gov with Vaneltix Pharma, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 2b, Open Label, Single-Arm, Multi-Center, Multiple Dose, 14-Day Study to Evaluate the Safety, Efficacy, and Frequency of Intravesical Administration of VNX001 in Acute Treatment of Subjects With Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) Who Have an Episode of Acute Bladder Pain of Moderate to Severe Intensity
- Lead sponsor
- Vaneltix Pharma, Inc.
- Phase
- Phase 2
- Overall status
- Recruiting
- Start date
- December 13, 2024
- Completion date
- June 30, 2026
- Enrollment
- 50 (estimated)
- Sites
- 5
Conditions
As the registry lists them; a condition with its own page is linked.
bladder pain syndrome, interstitial cystitis