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Completed

NCT Number: NCT05283135

High Dose Risankizumab for Psoriasis

This pilot study explores higher than standard doses of risankizumab for plaque psoriasis, to see effects on resident memory T cells and skin clearance.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Oregon Medical Research Center

Portland, Oregon, 97201, United States

About this study

This is a pilot study that explores whether higher initial doses of risankizumab (300 mg and 600 mg, 2 times and 4 times the standard initial doses for plaque psoriasis) can more effectively target resident memory T cells, a type of immune cell within psoriatic lesions, and whether this results in higher levels of completely clear skin and for longer periods of time following withdrawal of drug. It is believed that resident memory T cells in psoriatic skin contribute to the persistence of psoriasis. It is believed that if the study drug can more effectively eliminate these cells, better clearance of psoriasis may be achieved (when compared to standard initial doses of study drug).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject has provided written consent
  • Subject has the ability to comply with all study visits and procedures
  • Subject is at least 18 years of age
  • Subject has chronic stable plaque psoriasis for at least 6 months and with a severity of BSA greater than or equal to 10 and PASI greater than or equal to 12
  • Female subjects of child-bearing potential must have a negative urine test at screening and baseline. Female subjects must be either postmenopausal, or permanently surgically sterile, or for women of child-bearing potential practicing at least one form of birth control

Exclusion criteria

  • Breastfeeding or pregnant women, or women who plan to become pregnant during study period
  • Participation in any other clinical trial
  • Active infection with HIV, hepatitis B virus, or hepatitis C virus
  • Active infection with tuberculosis or untreated latent tuberculosis
  • History of known active cancer, other than non-melanoma skin cancer or cervical carcinoma in situ, in the past 3 years
  • History of drug or alcohol abuse in the past 6 months, as per investigator's assessment
  • History of suicidal ideation or attempts in the past 6 months
  • Presence of any concurrent illness, which in the opinion of the investigator, would place the patient at unnecessary safety risk during the trial or interfere with completion of the trial
  • Treatment with topical medications for psoriasis in the past 2 weeks
  • Treatment with oral medications for psoriasis in the past 4 weeks
  • Phototherapy for psoriasis in the past 4 weeks
  • Any prior treatment with Risankizumab
  • Treatment with biologic medications for psoriasis (other than Risankizumab) in the past 4 months

Treatment and study plan

Risankizumab

Drug

Risankizumab (Skyrizi) is an anti-IL-23 antibody being investigated for the treatment of multiple inflammatory diseases, including psoriasis, Crohn's disease, ulcerative colitis, and psoriatic arthritis.

Other names: Skyrizi

Primary outcomes

  1. CD8+ Trm1 Cells in Lesional Skin at Baseline and Week 52

    Time frame: 52 weeks

    The number of lesional CD8+ Trm1 cells at baseline and Week 52 was calculated by longitudinal single-cell RNA-sequencing of full-thickness skin biopsy samples. Uniform Manifold Approximation Projection (UMAP) was used for T cell subtype visualization and CD8+ Trm1 cells were identified as IFNγ+/CD8+/CD69+ T cells.

  2. CD8+ Trm17 Cells in Lesional Skin at Baseline and Week 52

    Time frame: 52 weeks

    The number of lesional CD8+ Trm17 cells at baseline and Week 52 was calculated by longitudinal single-cell RNA-sequencing of full-thickness skin biopsy samples. Uniform Manifold Approximation Projection (UMAP) was used for T cell subtype visualization and CD8+ Trm17 cells were identified as IFNγ+/CD8+/CD69+ T cells.

Secondary outcomes

  1. PASI 100 Results in Patients Receiving 4X Standard Induction Doses of Risankizumab vs. Those Receiving 2X Standard Induction Doses of Risankizumab.

    Time frame: Enrollment to Week 52

    The percentage of patients with Psoriasis Area and Severity Index (PASI) 100 (complete clearance) at Weeks 28, 40, and 52 in patients receiving 4X standard induction doses of risankizumab vs. those receiving 2X standard induction doses of risankizumab.

  2. Safety Events

    Time frame: Enrollment to Week 52

    Safety events over 52 weeks in patients receiving 4X standard induction doses of risankizumab vs. those receiving 2X standard induction doses of risankizumab.

Sponsors and collaborators

Lead sponsor

Oregon Medical Research Center

Other

Collaborators

  • AbbVie

Registry information

Official study title

Decreasing Resident Memory T Cells While Increasing Clinical Durability: Higher Induction Doses of Risankizumab for Moderate-to-severe Plaque Psoriasis

Acronym: KNOCKOUT

Important dates

Study start
2022
Primary completion
2023
Study completion
2024
First posted
Mar 16, 2022
Registry last updated
Oct 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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