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NCT05478499CompletedPhase 4

Efficacy and Safety of Deucravacitinib Versus Placebo in Participants With Moderate-to-severe Scalp Psoriasis

A Phase 3B/4, Multicenter, Randomized, Double-blind Placebo-controlled Study to Evaluate the Efficacy and Safety of Deucravacitinib in Participants With Moderate-to-severe Scalp Psoriasis (PSORIATYK SCALP)

Source: ClinicalTrials.gov · Last updated 28 Oct 2025

Brief summary (registry, in English)

The purpose of this study is to compare the efficacy and safety of deucravacitinib to placebo in participants with moderate-to-severe scalp psoriasis.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
154 (actual)
First submitted
27 Jul 2022
Start date
6 Oct 2022
Primary completion date
11 Jan 2024
Lead sponsor
Bristol-Myers Squibb
Diseases
Psoriasis
NCT number
NCT05478499
EudraCT number
2022-000797-26

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 154
  • From 6 Oct 2022 to the primary completion date, 11 Jan 2024
  • 29 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Target Disease Exceptions:
    • Has nonplaque psoriasis (ie, guttate, inverse, pustular, erythrodermic or drug-induced psoriasis) at Screening or Day 1 Other protocol-defined inclusion/exclusion criteria apply

Who the study is looking for

  • Men and women diagnosed with stable plaque psoriasis with scalp involvement 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
  • Moderate-to-severe scalp psoriasis as defined by scalp-specific Physician's Global Assessment (ss-PGA) ≥ 3; ≥ 20% scalp surface area (SSA); Psoriasis Scalp Severity Index (PSSI) ≥ 12 at the Screening visit and Day 1
  • ≥ 3% of Body Surface Area (BSA) involvement at the Screening visit and Day 1
  • Evidence of plaque psoriasis in a non-scalp area
  • Failed to respond to, or intolerant of ≥ 1 topical therapy for scalp psoriasis

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (29)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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Frankfurt am MainGermanyUnknown status
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HamburgGermanyUnknown status
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LübeckGermanyUnknown status
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MahlowGermanyUnknown status
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WittenGermanyUnknown status
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ParisFranceUnknown status
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Romans-sur-IsèreFranceUnknown status
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RouenFranceUnknown status
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LondonUnited KingdomUnknown status
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SalfordUnited KingdomUnknown status
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SouthamptonUnited KingdomUnknown status
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KrakowPolandUnknown status
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LodzPolandUnknown status
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RzeszówPolandUnknown status
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WroclawPolandUnknown status
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BeverlyUnited StatesUnknown status
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Bloomfield HillsUnited StatesUnknown status
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East WindsorUnited StatesUnknown status
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Hot SpringsUnited StatesUnknown status
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HoustonUnited StatesUnknown status
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IndianapolisUnited StatesUnknown status
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Kew GardensUnited StatesUnknown status
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LouisvilleUnited StatesUnknown status
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New BrightonUnited StatesUnknown status
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NorfolkUnited StatesUnknown status
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PittsburghUnited StatesUnknown status
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PortlandUnited StatesUnknown status
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RockvilleUnited StatesUnknown status
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San AntonioUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.