Skip to content

Psoriatic Inflammation Markers Predictive of Response to Adalimumab

Characterization of the Initial Psoriatic Skin Transcriptionnl Profile Associated to a Response to Adalimumab Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03389984
Acronym
IMPRA
Enrollment
85
Registered
2018-01-04
Start date
2017-11-14
Completion date
2020-06-18
Last updated
2020-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis Vulgaris

Brief summary

The objective is to compare the initial skin inflammatory transcriptomic profile of psoriatic patient responder to Adalimumab therapy (defined as the achievement of a Psoriasis Area and Severity Index 75 response at 16 weeks) with the transcriptomic profile of patient non-responder to Adalimumab therapy (defined as the non-achievement of a Psoriasis Area and Severity Index 50 response at 16 weeks) to identify differentially expressed genes in order to define predictive markers of response to the treatment.

Interventions

DIAGNOSTIC_TESTcutaneous

SKIN BIOPSY

Sponsors

Poitiers University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Chronic plaque psoriasis involving at least 10% of body surface area, with a PASI score \>10, * Negative pregnancy test for women of childbearing potential, and use of an effective method of contraception, * Pretreatment assessment to identify contraindications to anti-tumor necrosis factor-alpha therapy (chest x-ray and Intradermal reaction (detection of latent tuberculosis), * Anti-tumor necrosis factor-alpha treatment with adalimumab has been prescribed

Exclusion criteria

* Classical

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline messenger ribonucleic acid expression at 16 weeks of treatmentFrom baseline to 16 weeks treatmentmessenger ribonucleic acid expression assessed by quantitative reverse transcription-polymerase chain reaction

Secondary

MeasureTime frameDescription
Change from baseline drug and anti-drug concentrations at 16 weeks of treatmentFrom baseline to 16 weeks treatmentassessed by enzyme-linked-immunoassay

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026