Skin Transcriptional Profiles In Psoriatic Patients Under Adalimumab Biotherapy

NCT ID: NCT01872546

Last Updated: 2016-10-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Brief Summary

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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.

Detailed Description

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Conditions

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Chronic Plaque Psoriasis

Study Groups

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Adalimumab

Group Type EXPERIMENTAL

HUMIRA 40mg

Intervention Type DRUG

Interventions

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HUMIRA 40mg

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients with chronic plaque psoriasis involving at least 10% of body surface area with no previous biotherapy.
* Adalimumab prescribed in usual practice

Exclusion Criteria

* Patients presenting a contraindication to the use of Adalimumab:

hypersensibility in Adalimumab or in one of the excipients.

* Patients presenting an evolutionary tuberculosis or the other severe infections such as sepsis and opportunist infections
* presenting patients one cardiac insufficiencies moderated in severe
* Patients under anakinra or abatacept
* current participation in another study of clinical research
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Poitiers University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Chu Poitiers

Poitiers, , France

Site Status

Countries

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France

Other Identifiers

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CYTOPSO

Identifier Type: -

Identifier Source: org_study_id

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