A Study to Evaluate the Safety of Raptiva in Adults With Plaque Psoriasis Previously Enrolled in Study ACD2600g
This study has been completed.
Sponsor:
Genentech
Information provided by:
Genentech
ClinicalTrials.gov Identifier:
NCT00096603
First received: November 12, 2004
Last updated: November 14, 2005
Last verified: November 2005
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Purpose
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 |
|---|---|---|
|
Psoriasis |
Drug: Raptiva (efalizumab) |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety Study Masking: Open Label Primary Purpose: Treatment |
| 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 |
Resource links provided by NLM:
Further study details as provided by Genentech:
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Signed informed consent
- Previous participation in Study ACD2600g
- For women of childbearing potential, continued use of an acceptable method of contraception for the duration of the study
Exclusion Criteria:
- Any medical condition that, in the judgment of the investigator, would jeopardize the subject’s safety following exposure to Efalizumab
Contacts and Locations
No Contacts or Locations Provided
More Information
Additional Information:
Study Results 
No publications provided
| ClinicalTrials.gov Identifier: | NCT00096603 History of Changes |
| Other Study ID Numbers: | ACD2601g |
| Study First Received: | November 12, 2004 |
| Last Updated: | November 14, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Genentech:
|
Moderate to severe plaque psoriasis |
Additional relevant MeSH terms:
|
Psoriasis Skin Diseases, Papulosquamous Skin Diseases |
ClinicalTrials.gov processed this record on June 18, 2013