Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02462187 · ClinicalTrials.gov registry record · Phase 2

Topical NVN1000 for the Treatment of External Genital and Perianal Warts

A Phase 2 study of Genital Warts and Perianal Warts, sponsored by Novan.

Completed
Registry status
Phase 2
Development phase
108
Enrollment target
15
Study locations

NCT02462187: Completed Phase 2 study of Genital Warts and Perianal Warts, sponsored by Novan.

NCT02462187 is a Phase 2 study of Genital Warts and Perianal Warts that has completed, run by Novan. The registered enrollment target is 108 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (19% lower). The trial reports 15 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02462187, a Phase 2 study of Genital Warts and Perianal Warts, has completed, sponsored by Novan.

COMPLETED
Registry status
Phase 2
Development phase
108 participants
Enrollment target
15
Study locations

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

Primary Outcome

Clearance of baseline external genital and perianal warts at or before Week 12 as determined by physical examination by the investigator.

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

FieldValue
Enrollment Target 108 participants
Start Date 2015-06-12
Est. Completion 2016-10-17
Phase Phase 2
Novan

18 total trials

What the finished NCT02462187 record still lists

NCT02462187 is an interventional study that assigns participants to a tested intervention. The registered 108 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (19% lower).

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.

NCT02462187 lists 15 locations in 8 states (Texas, California, Georgia).

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.

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).

Who is sponsoring clinical trial NCT02462187?

This trial is sponsored by Novan, which has 18 total clinical trials registered on ClinicalTrials.gov.

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.

How this trial's enrollment target compares

Where NCT02462187's enrollment target sits among peer trials

108 640th of 2000 higher than 1,355 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02703207 · 108 participants · NA

    Neurocognitive and Health Impact of Sleep Apnea in Elderly Veterans With Comorbid COPD

  • NCT02744677 · 108 participants · NA

    COMPASSION S3 - Evaluation of the SAPIEN 3 Transcatheter Heart Valve in Patients With Pulmonary Valve Dysfunction

  • NCT02781883 · 108 participants · Phase 2

    Clinical Trial of BP1001 in Combination With With Venetoclax Plus Decitabine in AML

  • NCT03848663 · 108 participants · NA

    Visual Remapping to Aid Reading With Field Loss

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02462187, the US trial registry maintained by the National Library of Medicine. NCT02462187 (mid enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.