Evidence map›Paper›PMID 34652810›Full record

ArticleThe British journal of dermatology2022

Long-term safety of risankizumab from 17 clinical trials in patients with moderate-to-severe plaque psoriasis.

K B Gordon, M Lebwohl, K A Papp, H Bachelez, J J Wu, R G Langley, A Blauvelt, B Kaplan, M Shah, Y Zhao and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The British journal of dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 3 pooled it
5.3field-weighted citation impact, top 3% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 3 syntheses or guidelines pooled it, 98 citations in OpenAlex.

  1. Pooled it
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  9. Article
  10. Lung abscess as an adverse effect of Risankizumab.European clinical respiratory journal · 2026
    Article
  11. IL-23 Inhibitors in Psoriasis: What Have We Learnt so Far?Journal of inflammation research · 2026
    Review
  12. Article
  13. Risankizumab in Patients with Psoriasis with Current or Previous Malignancy: A Multicenter, Retrospective Real-World Study.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 9 institutions in 4 countries.

K B GordonDepartment of Dermatology, Medical College of Wisconsin, Milwaukee, WI, USA.ORCID 0000-0002-9347-0292
M LebwohlDepartment of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
K A PappK Papp Clinical Research and Probity Medical Research, Waterloo, ON, Canada.ORCID 0000-0001-9557-3642
H BachelezHôpital Saint-Louis, AP-HP, Université de Paris, Paris, France.
J J WuDermatology Research and Education Foundation, Irvine, CA, USA.
R G LangleyDivision of Dermatology, Department of Medicine, Dalhousie University, Halifax, NS, Canada.
A BlauveltOregon Medical Research Center, Portland, OR, USA.ORCID 0000-0002-2633-985X
B KaplanAbbVie Inc., North Chicago, IL, USA.
M ShahAbbVie Inc., North Chicago, IL, USA.
Y ZhaoAbbVie Inc., North Chicago, IL, USA.
R SinvhalAbbVie Inc., North Chicago, IL, USA.
K ReichCenter for Translational Research in Inflammatory Skin Diseases, Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-5248-4332
AbbVie (United States) · USDalhousie University · CADermatology Research and Education Foundation · USIcahn School of Medicine at Mount Sinai · USMedical College of Wisconsin · USOregon Medical Research Center · USProbity Medical Research · CAUniversität Hamburg · DEUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRisankizumab has demonstrated efficacy and safety in patients with moderate-to-severe plaque psoriasis in randomized clinical trials.

objectivesTo evaluate safety data from risankizumab psoriasis phase I-III clinical trials.

methodsShort-term safety (through week 16) was analysed using integrated data from five phase II and III clinical trials. Long-term safety was evaluated using integrated data from 17 phase I-III completed and ongoing trials.

resultsShort-term safety analyses included 1306 patients receiving risankizumab 150 mg and 300 patients receiving placebo [402·2 and 92·0 patient-years (PY) of exposure, respectively]. Long-term analyses included 3072 risankizumab-treated patients (exposure: 7927 PY). The median (excluding four outliers) treatment duration was 2·9 years (range 2 days to 5·9 years). Exposure-adjusted adverse event rates did not increase with long-term treatment (318 vs. 171 events per 100 PY for short- and long-term analyses). With long-term risankizumab treatment, rates of serious adverse events were 7·8 per 100 PY, serious infections 1·2 per 100 PY, nonmelanoma skin cancer (NMSC) 0·7 per 100 PY, malignant tumours excluding NMSC 0·5 per 100 PY, and adjudicated major adverse cardiovascular events 0·3 per 100 PY, with no important identified risks. Limitations include that the study inclusion and exclusion criteria varied and that three studies enrolled ≤ 50 patients.

conclusionsRisankizumab demonstrated a favourable safety profile over short- and long-term treatment in patients with moderate-to-severe psoriasis.

Indexed as

Antibodies, MonoclonalPsoriasisClinical Trials as TopicHumansSeverity of Illness IndexTreatment OutcomeAntibodies, Monoclonalrisankizumab

Identifiers

PMID34652810
PMCPMC9298814
OpenAlexW3207194448

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.