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A Long Term Follow up Study of Patients Who Have Completed the PEP005-016 or PEP005-025 Studies
NCT00953732 · View on ClinicalTrials.gov ↗
Study Summary
This study is designed to follow up patients who have achieved complete clearance of AK lesions at the Day 57 visit having completed the PEP005-016 or PEP005-025 studies over a 12 month period to assess both recurrence of Actinic Keratosis (AK) lesions and long term safety in the selected treatment area.
Conditions Studied
Interventions
- DRUG Lesion count
Study Locations (20)
California
- Center for Dermatology — Fremont
- Dermatology Research Associates — Los Angeles
- Dermatology Specialists Inc — Oceanside
- Skin Surgery Medical Group Inc. — San Diego
- Conant Medical Group — San Francisco
Indiana
- Laser Skin Surgery Center of Indiana — Carmel
- Deaconess Clinic, Inc — Evansville
- Dawes Fretein Clinical Research Group, LLC — Indianapolis
- The Indiana Clinical Trials Center, PC — Plainfield
Florida
- North Florida Dermatology Associates, PA — Jacksonville
- University of Miami, Skin Research Camp — Miami
Georgia
- Atlanta Dermatology, Vein & Research Center, LLC — Alpharetta
- Medaphase Inc — Newnan
Illinois
- Altman Dermatology Associates — Arlington Heights
- Glazer Dermatology — Buffalo Grove
Arizona
- Burke Pharmaceutical Research — Hot Springs
Kentucky
- Pedia Research LLC — Owensboro
Michigan
- Hamzavi Dermatology — Fort Gratiot
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 117 participants |
| Start Date | 2009-08 |
| Est. Completion | 2010-10 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00953732
The ClinicalTrials.gov registry entry for NCT00953732 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 117 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Peplin, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Actinic Keratosis appearing as the primary indexed condition, and to 1 intervention — of which Lesion count is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00953732 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Indiana, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00953732 about?
NCT00953732 is a clinical study titled "A Long Term Follow up Study of Patients Who Have Completed the PEP005-016 or PEP005-025 Studies". This study is designed to follow up patients who have achieved complete clearance of AK lesions at the Day 57 visit having completed the PEP005-016 or PEP005-025 studies over a 12 month period to assess both recurrence of Actinic Keratosis (AK) lesions and long term safety in the selected treatment ...
What is the current status of trial NCT00953732?
This trial is currently completed. The enrollment target is 117 participants. The study started on 2009-08. Estimated completion is 2010-10.
What conditions does trial NCT00953732 study?
This clinical trial studies the following conditions: Actinic Keratosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00953732?
The interventions under investigation include: Lesion count (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00953732?
This trial is sponsored by Peplin, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00953732 being conducted?
This trial has 20 study locations across Arizona, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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