Evidence map›Paper›PMID 41381642›Full record

Trial reportNature communications2025

A randomized phase 2 clinical trial to treat moderate-to-severe plaque psoriasis patients with high-induction dosing of risankizumab.

Andrew Blauvelt, Rundong Jiang, Linyu Shi, Lam C Tsoi, Rachael Bogle, Jennifer Fox, Mehrnaz Gharaee-Kermani, Allison C Billi, Robert T Matheson, Huzefa Photowala and 2 more

Registry-linked trialAbstract readClinical Trial, Phase IIRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05283135 (Decreasing Resident Memory T Cells While Increasing Clinical Durability), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05283135 phase2completednot on this map

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

TypeinterventionalSponsorOregon Medical Research CenterRan2022 to 2024Enrolled20ConditionsPsoriasisArmsrisankizumab
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. LCN2-Driven Fibroblast Ferroptosis-Associated Injury Promotes Keratinocyte Proliferation via Lipid Peroxidation Signaling in Psoriasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Article
  6. Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Andrew Blauvelt *Oregon Medical Research Center, Portland, OR, USA. blauveltconsults@gmail.com.ORCID http://orcid.org/0000-0002-2633-985X
Rundong Jiang *Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0009-0006-8296-4912
Linyu ShiAbbVie Inc, North Chicago, IL, USA.
Lam C TsoiDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.
Rachael BogleDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-3544-3023
Jennifer FoxDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.
Mehrnaz Gharaee-KermaniDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-2177-2427
Allison C BilliDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0001-7115-9113
Robert T MathesonOregon Medical Research Center, Portland, OR, USA.
Huzefa PhotowalaAbbVie Inc, North Chicago, IL, USA.
Johann E Gudjonsson *Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-0080-0812
Benjamin D Ehst *Oregon Medical Research Center, Portland, OR, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The phase 2 KNOCKOUT (NCT05283135) study evaluates higher-than-approved doses of risankizumab, an interleukin-23 inhibitor, for treatment of moderate-to-severe plaque psoriasis. Patients received either 300 or 600 mg of risankizumab at Weeks 0, 4, and 16 and were monitored for 100 weeks without further dosing. Efficacy and safety were tracked throughout the study and lesional/non-lesional tissue was evaluated by RNASeq. The primary endpoint was the change in baseline in number and/or function of tissue resident memory T cells (T

Indexed as

Antibodies, MonoclonalPsoriasisAdultAgedFemaleHumansInterleukin-23MaleMemory T CellsMiddle AgedSeverity of Illness IndexTreatment OutcomeAntibodies, MonoclonalInterleukin-23risankizumab

Identifiers

PMID41381642
PMCPMC12819383

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.