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Topical NVN1000 for the Treatment of External Genital and Perianal Warts
NCT02462187 · View on ClinicalTrials.gov ↗
Study Summary
A Phase 2 Multi-Center, Double-Blind, Randomized, Vehicle-Controlled, Ascending Dose Study Assessing Tolerability, Safety, and Efficacy of Topical NVN1000 in Subjects with External Genital Warts and Perianal Warts
Conditions Studied
Interventions
- DRUG Vehicle
- DRUG NVN1000 8% Gel
- DRUG NVN1000 16%
- DRUG NVN1000 24%
Study Locations (15)
Texas
- PPD 128 — Corpus Christi
- PPD 129 — Houston
- PPD 127 — San Antonio
- PPD 131 — Webster
California
- PPD 137 — Fountain Valley
- PPD 140 — Lomita
- PPD 133 — San Diego
Georgia
- PPD 134 — Atlanta
- PPD 139 — Atlanta
- PPD 138 — Roswell
Indiana
- PPD 130 — Indianapolis
Louisiana
- PPD 126 — Metairie
Oregon
- PPD 132 — Portland
Pennsylvania
- PPD 135 — Philadelphia
Washington
- PPD 136 — Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 108 participants |
| Start Date | 2015-06-12 |
| Est. Completion | 2016-10-17 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02462187
The ClinicalTrials.gov registry entry for NCT02462187 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 108 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novan, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Genital Warts appearing as the primary indexed condition, and to 4 interventions — of which Vehicle is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02462187 reports 15 study locations spanning 8 distinct geographic areas — top geographies include Texas, California, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02462187 about?
NCT02462187 is a clinical study titled "Topical NVN1000 for the Treatment of External Genital and Perianal Warts". A Phase 2 Multi-Center, Double-Blind, Randomized, Vehicle-Controlled, Ascending Dose Study Assessing Tolerability, Safety, and Efficacy of Topical NVN1000 in Subjects with External Genital Warts and Perianal Warts
What is the current status of trial NCT02462187?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 108 participants. The study started on 2015-06-12. Estimated completion is 2016-10-17.
What conditions does trial NCT02462187 study?
This clinical trial studies the following conditions: Genital Warts, Perianal Warts. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02462187?
The interventions under investigation include: Vehicle (DRUG), NVN1000 8% Gel (DRUG), NVN1000 16% (DRUG), NVN1000 24% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02462187?
This trial is sponsored by Novan, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02462187 being conducted?
This trial has 15 study locations across California, Georgia, Indiana, Louisiana, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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