Skin Transcriptional Profiles In Psoriatic Patients Under Adalimumab Biotherapy
- Sponsor
- Poitiers University Hospital
- Study ID
- NCT01872546
- Phase
- PHASE2
- Status
- Completed
Conditions
- Chronic Plaque Psoriasis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Adalimumab Every Week — DRUGAdalimumab was administered subcutaneously at a dose of 80 mg at Week 0 and 40 mg every other week starting from Week 1 to Week 16.
Study Details
The expertise in the characterization of transcriptomics profile in lesional psoriatic skin and on the availability of innovative therapy for these patients.The investigators propose to follow the modification of the skin transcriptomics profile in psoriatic patients during successful Adalimumab biotherapy. Skin transcriptomics profiles of normal skin, psoriatic non lesional skin, and psoriatic lesional skin before and after biotherapy will be compared. The investigators will focus on the modification of the cytokine "signature" in these skin lesions and of some markers of keratinocyte inflammation. The modification of the transcriptomics profile induced by the biotherapy will be correlated to the clinical response Psoriasis Area and Severity Index.
Key Dates
- Start date
- Jan 31, 2013
- Status verified
- Oct 2016
- Primary completion
- Apr 30, 2013
- Completion
- Sep 30, 2013
Study Design
- Enrollment
- 18 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: AdalimumabAdalimumab was administered subcutaneously at a dose of 80 mg at Week 0 and 40 mg every other week starting from Week 1 to Week 16.
Primary Outcome Measure
Area and Severity Index (PASI) [ Time Frame: 4 weeks ]
Related coverage on Hipa.ai
- Adalimumab Trial Measures PASI, DLQI in Chronic Plaque PsoriasisAdalimumab · Jun 24, 2026 · ClinicalTrials.gov