Psoriasis Clinical Trial

Transitioning From Cyclosporine to Alefacept in Psoriasis

Summary

The purpose of this study is to devise a safe and effective method for transitioning patients from cyclosporine to alefacept.

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Full 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.

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Eligibility Criteria

Inclusion Criteria

Adult psoriasis patients (18 to 80 years old), who are well controlled on cyclosporine (Static PGA score of mild, minimal or clear) and who need or desire to stop cyclosporine and start alefacept.

Exclusion Criteria

CD4 <400
Active infection (other than trivial URI, etc.)
History of AIDS or Hepatitis B, C
Inability to understand consent or comply with study requirements
Pregnancy or Lactation
History of heart or liver disease

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

13

Study ID:

NCT00143806

Recruitment Status:

Completed

Sponsor:

University of Medicine and Dentistry of New Jersey

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There is 1 Location for this study

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UMDNJ Clinical Research Center
New Brunswick New Jersey, 08903, United States

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

13

Study ID:

NCT00143806

Recruitment Status:

Completed

Sponsor:


University of Medicine and Dentistry of New Jersey

How clear is this clinincal trial information?

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