Safety, Pharmacokinetics, and Efficacy Study of NB-001 to Treat Recurrent Herpes Labialis

NCT00453401 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2008-05-30

No results posted yet for this study

Summary

Purpose of this study is to determine the safety and efficacy of topical applications of NB-001 as compared to placebo for the treatment of recurrent herpes labialis.

Conditions

  • Herpes Labialis

Interventions

DRUG

NB-001

Sponsors & Collaborators

  • NanoBio Corporation

    lead INDUSTRY

Principal Investigators

  • William Abramovits, MD · Dermatology Treatment and Research Center

  • Jeffrey Adelglass, MD · Research Across America

  • Maurice Archuleta, MD · Front Range Clinical Research

  • Brian Bock, DO · Bock Clinical Research Incorporated

  • Alicia Bucko, DO · Academic Dermatology Associates

  • Teresa Coats, MD · Benchmark Research

  • Lisa Cohen, DO · Suncoast Clinical Research

  • John Eck, MD · Advanced Clinical Research Incorporated

  • Douglass Forsha, MD · South Valley Dermatology Center

  • David Fried, MD · Omega Medical Research

  • Helen Henry, MD · Westover Heights Clinic

  • Michael T Jarratt, MD · Derm Research Incorporated

  • Terry Jones, MD · J & S Studies

  • Steven Kaster, MD · Wenatchee Valley Medical Center

  • Leon Kircik, MD · DermResearch, PLCC

  • Ronica Kluge, MD · Clinical Physiology Associates

  • Elias Kolettis, MD · Clinical Research of West Florida

  • Oswald Mikell, MD · Okati Research Center, LLC

  • Eugene Monroe, MD · Advance Healthcare

  • Edward Pornoy, MD · Westlake Medical Research

  • Harvey Resnick, MD · R/D Clinical Research Incorporated

  • Dennis Riff, MD · Advanced Clinical Research Institute

  • Mark A Ringold, MD · New River Valley Research Institute

  • Ronald Savin, MD · PC

  • Daniel Stewart, MD · MI Center for Skin Care Research

  • Cynthia B Strout, MD · Coastal Carolina Research Center

  • Wayne Harper, MD · Wake Research Associates, LLM

  • Timothy Howard, MD · Medical Affiliated Reseach Center Incorporated

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2007-12-31
Completion
2007-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00453401 on ClinicalTrials.gov