A Study to Evaluate Raptiva in Combination With Topical Psoriasis Therapies

Psoriasis Clinical Trial

Official title:

An Open Label, Randomized, Multicenter Study to Evaluate the Safety, Tolerability, and Efficacy of Subcutaneously Administered Efalizumab Used in Combination With Topical Psoriasis Therapies for Prolonged Maintenance Treatment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00096980
• Other study ID #: ACD2243g
• Status: Completed
• Phase: Phase 4
• First received: November 17, 2004
• Last updated: June 19, 2013
• Start date: February 2001
• Est. completion date: May 2004

Study information

• Verified date: June 2013
• Source: Genentech, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This study is an open label, randomized, multicenter study designed to compare the efficacy of 12 weeks of subcutaneously administered efalizumab (monotherapy) with that of combination therapy (Efalizumab and a topical corticosteroid ointment) in subjects with moderate to severe plaque psoriasis who are candidates for systemic therapy. The study will also evaluate the safety and tolerability of 30 months of continuous efalizumab treatment in those subjects who derive benefit from the initial 12 weeks of treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 300
• Est. completion date: May 2004
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Signed informed consent

• Diagnosis of plaque psoriasis for >=6 months

• A minimum Psoriasis Area and Severity Index (PASI) score of 12.0 at screening

• Plaque psoriasis covering >=10% of total Body Surface Area (BSA)

• In the opinion of the investigator, candidate for systemic therapy for psoriasis who has not been previously treated (naive to systemic treatment) or who has received prior systemic therapy for psoriasis (e.g., PUVA, cyclosporine, corticosteroids, methotrexate, oral retinoids, mycophenolate mofetil [MMF], thioguanine, hydroxyurea, sirolimus, azathioprine, 6 MP, etanercept)

• 18 to 70 years old

Exclusion Criteria:

• Guttate, erythrodermic, or pustular psoriasis as sole or predominant form of psoriasis

• Clinically significant psoriasis flare during the 3 months prior to enrollment

• Pregnancy or lactation

• History of or ongoing uncontrolled bacterial, viral, fungal, or atypical mycobacterial infection

• History of opportunistic infections (e.g., systemic fungal infections, parasites)

• Seropositivity for hepatitis B or C virus

• Seropositivity for human immunodeficiency virus (HIV)

• History of active tuberculosis (TB) or currently undergoing treatment for TB

• Presence or history of malignancy within the past 5 years, including lymphoproliferative disorders

• Diagnosis of hepatic cirrhosis, regardless of cause or severity

• Hospital admission for cardiovascular or pulmonary disease within the last year

• History of substance abuse within the last 5 years

• History of severe allergic or anaphylactic reactions to monoclonal antibodies or fusion proteins, which contain an immunoglobulin (Ig) Fc region (e.g., etanercept, LFA3TIP)

• History of severe allergic reactions to or intolerance of topical corticosteroid therapies

• Previous treatment with efalizumab

• History of treatment with lymphocyte-depleting monoclonal antibodies or immunoadhesion molecules (e.g., anti-CD4, CTLA4-Ig, LFA3TIP)

• WBC count <4000/uL or >14,000/uL

• Hepatic enzymes >=3 times the upper limit of normal

• Creatinine >=2 times the upper limit of normal

• Any medical condition that, in the judgment of the investigator, would jeopardize the subject's safety following exposure to study drug

• Any medical or other condition that, in the judgment of the investigator, would significantly interfere with the subject's ability to comply with the provisions of this protocol

• Topical therapy for psoriasis

• Systemic therapy for psoriasis

• Systemic immunosuppressive drugs

• Tanning beds, booths, or home UV light sources

• Live virus or bacteria vaccine

• Other vaccines or allergy desensitization injections

• Other experimental drugs or treatments

• Nonsteroidal anti inflammatory drugs

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Psoriasis

Intervention

Drug:
• Raptiva (efalizumab)

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Genentech, Inc.