Last updated on July 2018

REVEAL 1 (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL)

Brief description of study

HPV-301 is a prospective, randomized, double-blind, placebo controlled Phase 3 study to determine the efficacy, safety, and tolerability of VGX-3100 administered by intramuscular (IM) injection followed by electroporation (EP) delivered with CELLECTRA 5PSP in adult women with histologically confirmed cervical high grade squamous intraepithelial lesion (HSIL) (cervical intraepithelial neoplasia grade 2 [CIN2] or grade 3 [CIN3]) associated with human papillomavirus (HPV) 16 and/or HPV-18.

Clinical Study Identifier: NCT03185013

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Danilo Herrera

Coastal Clinical Research Inc
Mobile, AL United States
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Ernesto Gomez

Mesa Obstetricians and Gynecologist
Mesa, AZ United States
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Cynthia Goldberg

Visions Clinical Research-Tucson
Tucson, AZ United States
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Edward Zbella

Women's Medical Research Group, LLC
Clearwater, FL United States
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Samuel Lederman

Altus Research
Lake Worth, FL United States
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Ronald Ackerman

Comprehensive Clinical Trials LLC
West Palm Beach, FL United States
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Daron Ferris

Augusta University
Augusta, GA United States
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Christine Sanders

Hutchinson Clinic
Hutchinson, KS United States
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Kevin Ault

University of Kansas Medical Center
Kansas City, KS United States
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Clifton Nicholson-Uhl

Praetorian Pharmaceutical Research, LLC
Marrero, LA United States
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Robert Jeanfreau

Metairie, LA United States
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Thomas Minnec

Saginaw Valley Medical Research Group LLC
Saginaw, MI United States
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Keith Vrbicky

Meridian Clinical Research Norfolk
Norfolk, NE United States
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Mark Einstein

New Jersey Medical School
Newark, NJ United States
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Ana Tergas

Columbia University Medical Center
New York, NY United States
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Kenneth Levey

New York Pelvic Pain and Minimally Invasive Gynecologic Surgery PC
New York, NY United States
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Lance Edwards

Suffolk Obstetrics and Gynecology
Port Jefferson, NY United States
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Andrea Lukes

Carolina Women's Research and Wellness Center
Durham, NC United States
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Robert Parker

Lyndhurst Clinical Research
Winston-Salem, NC United States
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Katherine Smith

The University of Oklahoma Health Sciences Center
Oklahoma City, OK United States
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David Godwin

Greenville Pharmaceutical Research, Inc.
Greenville, SC United States
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Helena Kirkpatrick

Magnolia Ob/Gyn Research Center, LLC
Myrtle Beach, SC United States
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Kirk Brody

Chattanooga Medical Research Inc
Chattanooga, TN United States
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Belvia Carter

Women's Physician Group
Memphis, TN United States
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Sandra Hurtado

The Woman's Hospital of Texas
Houston, TX United States
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Kourtney Sims

BI Research Center
Houston, TX United States
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Mohamad Parva

Group For Women
Norfolk, VA United States
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James Rice

Multicare Health System
Covington, WA United States
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Josefina Romaguera

Puerto Rico Translational Research Center (PRTRC)
Rio Piedras, Puerto Rico
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Micah Harris

Women's Health Research
Scottsdale, AZ United States
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Jacob Tangir

Salom and Tangir LLC
Miramar, FL United States
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Unified Women's Clinical Research Raleigh
Raleigh, NC United States
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Stephen DePasquale

Chattanooga's Program In Women's Oncology
Chattanooga, TN United States
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Study Coordinator Ivette Santiago

Hope Clinical Research LLC
Kissimmee, FL United States
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Principal Investigator Nelson Uzquiano

UAG Innovation Women Research, LLC
Houston, TX United States
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Eastern Virginia Medical School
Norfolk, VA United States
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