Overview
Trial of an Injectable Biologic and U0279 as Combination Therapy for Severe Plaque-Type Psoriasis
Status:
Withdrawn
Withdrawn
Trial end date:
2010-04-01
2010-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of the study is to assess the safety and efficacy of an injectable biologic and U0279 as combination therapy compared to that of an injectable biologic alone for severe plaque-type psoriasis.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Stiefel, a GSK CompanyCollaborator:
GlaxoSmithKlineTreatments:
Acitretin
Etanercept
Criteria
Inclusion Criteria:- Male or female subjects 18 years of age or older.
- Surgically sterile females. Females who have had a hysterectomy or completed menopause
are allowed.
- Affected Body Surface Area with psoriasis of ≥10%.
- Psoriasis Global Assessment rating of "moderate to severe" or "severe".
- Achieved mild to moderate improvement after receiving an injectable biologic therapy
for at least 12 weeks.
- A PASI score of ≥ 50 and ≤75
- Capable of understanding and willing to provide signed and dated written voluntary
informed consent (and any local or national authorization requirements) before any
protocol specific procedures are performed
Exclusion Criteria:
- Understand that the sponsor can not pay for the an injectable biologic therapy during
the course of the study; be willing to pay out of pocket or secure payment through
their private health insurance for an injectable biologic.
- History of systemic infection, or other conditions that may interfere with study
evaluations or may increase risk for participation. such as, tuberculosis, human
immunodeficiency virus (HIV), hepatitis; congestive heart failure or demyelinating
disorder.
- Used of prohibited medications or therapies