Trials / Completed
CompletedNCT00143806
Transitioning From Cyclosporine to Alefacept in Psoriasis
Investigator-Initiated, Use Study of Alefacept (Amevive) in Combination With Tapering Doses of Cyclosporine in Patients With Moderate to Severe Psoriasis
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 13 (planned)
- Sponsor
- University of Medicine and Dentistry of New Jersey · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to devise a safe and effective method for transitioning patients from cyclosporine to alefacept.
Detailed description
The purpose of this study is to devise a safe and effective method for transitioning patients from cyclosporine to alefacept. Patients in the study are well controlled on cyclosporine and desire to switch to alefacept. The study is done in three phases. In Phase 1 (12 week duration) the two drugs will be overlapped, with cyclosporine slowly tapering. Both drugs will be discontinued after 12 weeks. In Phase 2 (12 weeks duration), patients are off both drugs. In Phase 3 (24 weeks long), patients are on a second course of alefacept alone for 12 weeks and then off for 12 weeks. Topical and UV light treatments are allowed throughout the study. Total length of study is one year.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Transitioning patients from cyclosporine to alefacept |
Timeline
- Start date
- 2003-10-01
- Completion
- 2007-05-01
- First posted
- 2005-09-02
- Last updated
- 2009-01-05
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00143806. Inclusion in this directory is not an endorsement.