RECRUITINGOBSERVATIONAL
Exploration of the Cellular and Molecular Mechanisms in Patients Receiving Biotherapies Targeting the IL-23/IL-17 Axis in Cutaneous Psoriasis
About This Trial
This is a research study involving humans, of the interventional type with minimal risks and constraints (RIPH2). It is a monocentric, non randomized prospective study aiming to better understand the mechanisms of the response to anti-IL-23 biologics in psoriasis patients attending the dermatology department of hospital Cochin (APHP).
Who May Be Eligible (Plain English)
Who May Qualify:
All patients:
- Adults (\>18 years)
- Presenting with cutaneous psoriasis
- Patients have signed an willing to sign a consent form
- Beneficiary of the health insurance, except for the AME Only for patients of Group 1
- Patients require systemic treatment for psoriasis
- Patients are naïve to biological therapies
Only for patients of Group 2:
- Patients requiring treatment with anti-IL-23 biologics (guselkumab, risankizumab, tildrakizumab) upon referent physician's decision.
- Patients are naïve to biological therapies or have received only one biologic, with a "wash-out" period of at least 4 months
Non Who May Qualify:
For all :
- Patient is minor
- Patient is pregnant or breastfeeding
- Patient is immunocompromised
- Patient is under legal protection, curatorship, guardianship
- Patient refuses consent
- Patient is unable to comply with study requirements for geographic, social or psychiatric reason.
- Beneficiary of the AME Only for patients of Group 1
- Patient has received biologics Only for patients of Group 2
- Patient has a contraindication to the chosen biotherapy
- Patient has received biologics within the last 4 months
- Patient has been treated with 2 or more biologics
- Patient has already received an anti-IL-23 biologic
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
All patients:
* Adults (\>18 years)
* Presenting with cutaneous psoriasis
* Patients have signed an informed consent
* Beneficiary of the health insurance, except for the AME Only for patients of Group 1
* Patients require systemic treatment for psoriasis
* Patients are naïve to biological therapies
Only for patients of Group 2:
* Patients requiring treatment with anti-IL-23 biologics (guselkumab, risankizumab, tildrakizumab) upon referent physician's decision.
* Patients are naïve to biological therapies or have received only one biologic, with a "wash-out" period of at least 4 months
Non inclusion Criteria:
For all :
* Patient is minor
* Patient is pregnant or breastfeeding
* Patient is immunocompromised
* Patient is under legal protection, curatorship, guardianship
* Patient refuses consent
* Patient is unable to comply with study requirements for geographic, social or psychiatric reason.
* Beneficiary of the AME Only for patients of Group 1
* Patient has received biologics Only for patients of Group 2
* Patient has a contraindication to the chosen biotherapy
* Patient has received biologics within the last 4 months
* Patient has been treated with 2 or more biologics
* Patient has already received an anti-IL-23 biologic
Treatments Being Tested
OTHER
Blood sample
Blood will be collected in tubes heparinés BD (Vacutainer), homogenised, and immediately transported at room temperature to Institut Pasteur to be further processed
OTHER
Data collection
collection of socio-demographic, clinical and biological data.
OTHER
skin biopsies
skin biopsies of 4 mm in diameter. These samples will not be taken on the face or in an area of skin folds
Locations (1)
Lars ROGGE
Paris, Île-de-France Region, France