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NCT00817219 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy of TACLONEX Ointment in Adolescent Patients (Aged 12 to 17 Years) With Psoriasis Vulgaris
A Phase 2 study of Psoriasis Vulgaris, sponsored by LEO Pharma.
- Completed
- Registry status
- Phase 2
- Development phase
- 33
- Enrollment target
- 8
- Study locations
NCT00817219: Completed Phase 2 study of Psoriasis Vulgaris, sponsored by LEO Pharma.
NCT00817219 is a Phase 2 study of Psoriasis Vulgaris that has completed, run by LEO Pharma. The registered enrollment target is 33 participants, below the 87-participant average among 6 other Psoriasis Vulgaris trials with a reported enrollment target (62% lower). The trial reports 8 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00817219, a Phase 2 study of Psoriasis Vulgaris, has completed, sponsored by LEO Pharma.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 33 participants
- Enrollment target
- 8
- Study locations
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.
Primary Outcome
The number of participants experiencing each type of adverse drug reaction. Adverse drug reactions were defined as adverse events for which the investigator had not described the causal relationship to trial medication as "not related".
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 |
What the finished NCT00817219 record still lists
NCT00817219 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 87-participant average among 6 other Psoriasis Vulgaris trials with a reported enrollment target (62% lower).
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.
NCT00817219 lists 8 locations in 6 states (California, Texas, Florida).
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.
What interventions are being tested in trial NCT00817219?
The interventions under investigation include: Calcipotriene plus betamethasone dipropionate ointment (DRUG).
Who is sponsoring clinical trial NCT00817219?
This trial is sponsored by LEO Pharma, which has 65 total clinical trials registered on ClinicalTrials.gov.
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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