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NCT01902303 · ClinicalTrials.gov registry record · Phase 2

Evaluation of Cold Sore Treatments on Ultra Violet (UV) Induced Cold Sores

A Phase 2 study of Oral Herpes Simplex, sponsored by Beech Tree Labs.

Completed
Registry status
Phase 2
Development phase
303
Enrollment target
3
Study locations

NCT01902303 is a Phase 2 study of Oral Herpes Simplex that has completed, run by Beech Tree Labs. The registered enrollment target is 303 participants. The trial reports 3 study locations across 3 states.

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The verdict

NCT01902303, a Phase 2 study of Oral Herpes Simplex, has completed, sponsored by Beech Tree Labs.

COMPLETED
Registry status
Phase 2
Development phase
303 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this study is to determine if a new drug treatment is effective to block the development of a cold sore lesion following Ultra Violet (UV) exposure.

Conditions Studied

Interventions

  • DRUG Matching Placebo
  • DRUG BTL-TML-HSV

Study Locations (3)

Florida

  • Hill Top Research - St. Petersburg

Ohio

  • Hill Top Research - Cincinnati

South Carolina

  • Coastal Carolina Research Center - Mt. Pleasant

Trial Details

FieldValue
Enrollment Target 303 participants
Start Date 2013-07
Est. Completion 2015-02
Phase Phase 2

Sponsor

Beech Tree Labs

4 total trials

What the Registry Record Tells You About NCT01902303

The ClinicalTrials.gov registry entry for NCT01902303 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 303 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beech Tree Labs, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Oral Herpes Simplex appearing as the primary indexed condition, and to 2 interventions - of which Matching Placebo is the first listed.

NCT01902303 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Florida, Ohio, South Carolina.

Frequently Asked Questions

What is clinical trial NCT01902303 about?

NCT01902303 is a clinical study titled "Evaluation of Cold Sore Treatments on Ultra Violet (UV) Induced Cold Sores". The purpose of this study is to determine if a new drug treatment is effective to block the development of a cold sore lesion following Ultra Violet (UV) exposure.

What is the current status of trial NCT01902303?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 303 participants. The study started on 2013-07. Estimated completion is 2015-02.

What conditions does trial NCT01902303 study?

This clinical trial studies the following conditions: Oral Herpes Simplex.

What interventions are being tested in trial NCT01902303?

The interventions under investigation include: Matching Placebo (DRUG), BTL-TML-HSV (DRUG).

Who is sponsoring clinical trial NCT01902303?

This trial is sponsored by Beech Tree Labs, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01902303 being conducted?

This trial has 3 study locations across Florida, Ohio, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.