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RESTORE: Raptiva® (Efalizumab) Evaluation of Safety and Treatment Optimization
This study has been terminated.
( The study was terminated after the EMEA recommended to suspend the marketing authorisation of Raptiva in the EU )
Study NCT00402818 Information provided by Merck KGaA
First Received on November 20, 2006. Last Updated on December 15, 2009
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Plaque Psoriasis
Additional conditions recognized in this trial
Psoriasis
More general conditions related to this trial
Skin Diseases
Skin Diseases, Papulosquamous
Sponsors listed in this trial
Merck KGaA
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