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Completed Phase 2Phase 3 Interventional Results available

A Study to Evaluate Two Concentrations of DFD-07 Cream, in Subjects With Actinic Keratosis (AK) of the Face and/or Scalp Over a 12-week Treatment Period

ClinicalTrials.gov ID: NCT03116698

Public ClinicalTrials.gov record NCT03116698. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:44 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Double-Blind, Parallel-Group, Vehicle-Controlled Study to Evaluate the Dose-Response Relationship of the Efficacy and Safety of Two Concentrations of DFD-07 Cream, in Subjects With Actinic Keratosis (AK) of the Face and/or Scalp Over a 12-week Treatment Period.

Study identification

NCT ID
NCT03116698
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Dr. Reddy's Laboratories Limited
Industry
Enrollment
240 participants

Conditions and interventions

Interventions

  • Low dose DFD07 once daily Drug
  • High dose DFD07 once daily Drug
  • High dose DFD07 twice daily Drug
  • Placebo twice daily Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 13, 2017
Primary completion
Nov 12, 2017
Completion
Jul 4, 2018
Last update posted
Apr 23, 2019

2017 – 2018

United States locations

U.S. sites
20
U.S. states
6
U.S. cities
17
Facility City State ZIP Site status
Investigator Site 3 Cerritos California 90703
Investigator Site 1 Fremont California 94538
Investigator Site 9 Palm Springs California 92262
Investigator Site 18 Santa Ana California 92701
Investigator Site 16 Boca Raton Florida 33486
Investigator Site 8 Lake City Florida 32055
Investigator Site 7 Miami Florida 33126
Investigator Site 19 Miami Florida 33162
Investigator Site 20 Miami Lakes Florida 33016
Investigator Site 17 Ormond Beach Florida 32174
Investigator Site 6 West Palm Beach Florida 33409
Investigator Site 13 Verona New Jersey 07044
Investigator Site 15 Stony Brook New York 11790
Investigator Site 14 Fort Washington Pennsylvania 19034
Investigator Site 10 Austin Texas 78660
Investigator Site 4 Houston Texas 77055
Investigator Site 5 Plano Texas 75024
Investigator Site 11 San Antonio Texas 78229
Investigator Site 2 San Antonio Texas 78229
Investigator Site 12 San Antonio Texas 78249

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03116698, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 23, 2019 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03116698 live on ClinicalTrials.gov.

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