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Sponsored by: |
Genentech |
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Information provided by: | Genentech |
ClinicalTrials.gov Identifier: | NCT00096603 |
This is an open label, multicenter study designed to evaluate the safety and tolerability of efalizumab administered subcutaneously at weekly doses of 1.0 mg/kg in subjects with plaque psoriasis who previously participated in Study ACD2600g.
Condition | Intervention | Phase |
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Psoriasis |
Drug: Raptiva (efalizumab) |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Open Label, Safety Study |
Official Title: | An Open Label, Multicenter Study to Evaluate the Safety of 1.0 Mg/Kg Subcutaneously Administered Efalizumab in Adults With Plaque Psoriasis Previously Enrolled in Study ACD2600g |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | ACD2601g |
Study First Received: | November 12, 2004 |
Last Updated: | November 14, 2005 |
ClinicalTrials.gov Identifier: | NCT00096603 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Moderate to severe plaque psoriasis |
Skin Diseases Psoriasis Skin Diseases, Papulosquamous |
Skin Diseases Psoriasis Skin Diseases, Papulosquamous |