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An Open-Label Study to Evaluate Whether a Short-Term Course of Methotrexate in Psoriasis Patients Treated With Efalizumab is Safe and Increases Efficacy
To evaluate whether a short-term course of methotrexate in patients treated with efalizumab (Raptiva) increases efficacy. The secondary objectives of this study are 1) to evaluate the efficacy of Raptiva in maintaining the clinical improvement induced by short-term treatment with combination therapy of Raptiva and methotrexate 2) to evaluate the safety of short-term combination therapy of Raptiva and methotrexate.
The primary objective of this study is to evaluate whether a short-term course of methotrexate in patients treated with efalizumab (Raptiva) increases efficacy. The secondary objectives of this study are 1) to evaluate the efficacy of Raptiva in maintaining the clinical improvement induced by short-term treatment with combination therapy of Raptiva and methotrexate 2) to evaluate the safety of short-term combination therapy of Raptiva and methotrexate. The design of this study is to gain better control of the disease process while reducing potential toxicities by beginning treatment with Raptiva and adding methotrexate to those patients who do not improve significantly
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
University of California, Davis Medical Center Department of Dermatology
Sacramento, California, United States
Start Date
January 1, 2007
Primary Completion Date
May 1, 2008
Completion Date
May 1, 2008
Last Updated
June 14, 2018
12
ACTUAL participants
Methotrexate
DRUG
Raptiva
DRUG
Lead Sponsor
University of California, Davis
Collaborators
NCT07449234
NCT07116967
NCT07250802
Data Source & Attribution
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