Psoriasis (ARTISTYK Study)

Study Description

Brief Summary

The purpose of this study is to evaluate the effect of deucravacitinib on quality of life (QoL) in participants with plaque psoriasis in a community setting.

Condition or Disease

Psoriasis

Study Design

Study Type:	Interventional
Estimated Enrollment:	250 participants
Allocation:	Randomized
Intervention Model:	Parallel Assignment
Masking:	Double (Participant, Investigator)
Primary Purpose:	Treatment
Official Title:	A Study to Evaluate the Effect of Deucravacitinib on Quality of Life in Participants With Plaque Psoriasis in a Community Setting
Actual Study Start Date:	January 2023
Estimated Primary Completion Date:	April 2024
Estimated Study Completion Date:	January 2025

Eligibility Criteria

Ages Eligible for Study:	18 Years and older (Adult, Older Adult)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	No

Inclusion Criteria

Men and women diagnosed with stable plaque psoriasis for 6 months or more. Stable psoriasis is defined as no morphology changes or significant flares of disease activity in the opinion of the investigator. Deemed by the investigator to be a candidate for phototherapy or systemic therapy. ≥ 3% of Body Surface Area (BSA) involvement at Screening Visit and Day 1 Dermatology Life Quality Index (DLQI) score > 5 at Screening Visit and Day 1

Exclusion Criteria

Target Disease Exceptions: Non-plaque psoriasis (that is, guttate, pustular, erythrodermic, palmoplantar only involvement or drug-induced psoriasis) at Screening Visit or Day 1 Other protocol-defined inclusion/exclusion criteria apply.

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Study Description

Brief Summary

Condition or Disease

Study Design

Eligibility Criteria

Inclusion Criteria

Exclusion Criteria

Application for Clinical Trials

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