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Safety and Efficacy of TACLONEX Ointment in Adolescent Patients (Aged 12 to 17 Years) With Psoriasis Vulgaris
NCT00817219 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the safety and efficacy of 4 weeks of TACLONEX ointment in adolescent patients with psoriasis vulgaris.
Conditions Studied
Interventions
- DRUG Calcipotriene plus betamethasone dipropionate ointment
Study Locations (8)
California
- Center for Dermatology Clinical Research — Fremont
- University of California at San Diego/Rady Children's Hospital — San Diego
Texas
- Arlington Research Center — Arlington
- University of Texas-Dermatology — Houston
Florida
- Ameriderm Research — Maitland
Illinois
- Northwestern University's Feinberg School of Medicine — Chicago
Virginia
- Virginia Clinical Research, Inc. — Norfolk
Washington
- DBA Dermatology Associates — Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2009-07 |
| Est. Completion | 2011-12 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00817219
The ClinicalTrials.gov registry entry for NCT00817219 describes a study currently listed as completed. It is categorized as Phase 2, 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 33 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is LEO Pharma, which has 39 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 Psoriasis Vulgaris appearing as the primary indexed condition, and to 1 intervention — of which Calcipotriene plus betamethasone dipropionate ointment 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: NCT00817219 reports 8 study locations spanning 6 distinct geographic areas — top geographies include California, Texas, 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 NCT00817219 about?
NCT00817219 is a clinical study titled "Safety and Efficacy of TACLONEX Ointment in Adolescent Patients (Aged 12 to 17 Years) With Psoriasis Vulgaris". The purpose of this study is to evaluate the safety and efficacy of 4 weeks of TACLONEX ointment in adolescent patients with psoriasis vulgaris.
What is the current status of trial NCT00817219?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 33 participants. The study started on 2009-07. Estimated completion is 2011-12.
What conditions does trial NCT00817219 study?
This clinical trial studies the following conditions: Psoriasis Vulgaris. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00817219?
The interventions under investigation include: Calcipotriene plus betamethasone dipropionate ointment (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00817219?
This trial is sponsored by LEO Pharma, which has 39 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00817219 being conducted?
This trial has 8 study locations across California, Florida, Illinois, Texas, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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