Viewing Study NCT00109317



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Last Modification Date: 2024-10-26 @ 9:11 AM
Study NCT ID: NCT00109317
Status: COMPLETED
Last Update Posted: 2013-06-21
First Post: 2005-04-27

Brief Title: A Study to Evaluate Raptiva in Adults With Moderate to Severe Plaque Psoriasis Who Are Candidates for Systemic Therapy
Sponsor: Genentech Inc
Organization: Genentech Inc

Study Overview

Official Title: A Phase IIIb Randomized Double-Blind Parallel-Group Placebo-Controlled Multicenter Study to Evaluate the Safety of 10 mgkg Subcutaneously Administered Efalizumab in Adults With Moderate to Severe Plaque Psoriasis Who Are Candidates for Systemic Therapy
Status: COMPLETED
Status Verified Date: 2013-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a Phase IIIb randomized double-blind parallel-group placebo-controlled multicenter study designed to evaluate the safety and tolerability of efalizumab administered subcutaneously at weekly doses of 10 mgkg in subjects with moderate to severe plaque psoriasis who are candidates for systemic therapy
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None