Evidence map›Paper›PMID 42840331›Full record

ArticleJMA journal2026

Efficacy and Safety of Icotrokinra (an Interleukin-23 Inhibitor) in the Management of Moderate-to-Severe Plaque Psoriasis: A Systematic Review and Meta-Analysis.

Zain Ahmad Siddiqi, Sume Rubab, Faisal Jamal Alashkar, Ayesha Iqbal, Niam Adam Abubakr Mahdi, Maheen Haque, Rutbah Amin Khairati, Tosin Ayantoyinbo, Kainat Qasim, Muhammad Ahmad Shahzaib and 4 more

Abstract read
In one paragraph

Article in JMA journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Zain Ahmad SiddiqiDepartment of Medicine, Allama Iqbal Medical College, Lahore, Pakistan.
Sume RubabDepartment of Dermatology, Mayo Hospital, Lahore, Pakistan.
Faisal Jamal AlashkarDepartment of Medicine, Almaarefa University, Diriyah, Saudi Arabia.
Ayesha IqbalDepartment of Medicine, Royal Shrewsbury Hospital, Shrewsbury, United Kingdom.
Niam Adam Abubakr MahdiDepartment of Medicine, Hull University Teaching Hospitals NHS Trust, Hull, United Kingdom.
Maheen HaqueDepartment of Medicine, Dow International Medical College, Karachi, Pakistan.
Rutbah Amin KhairatiDepartment of Internal Medicine, George Eliot Hospital, Nuneaton, United Kingdom.
Tosin AyantoyinboDepartment of Internal Medicine, BronxCare Health System, New York, United States.
Kainat QasimDepartment of Medicine, Al-Nafees Medical College and Hospital, Islamabad, Pakistan.
Muhammad Ahmad ShahzaibDepartment of Internal Medicine, Henan Medical University, Xinxiang, China.
Anas Jamshed KhanDepartment of Anaesthesia, Buch International Hospital, Multan, Pakistan.
Fathima MasharifaDepartment of Medicine, Sheikh Khalifa Medical City Hospital, Abu Dhabi, United Arab Emirates.
Muaz Shafique Ur RehmanDepartment of Medicine, Jinnah Hospital, Lahore, Pakistan.
Fatimah HabibDepartment of Medicine, Scarborough General Hospital, Scarborough, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Plaque psoriasis, which is a chronic immune-mediated inflammatory skin condition, significantly reduces patients' quality of life. The cytokine interleukin-23 (IL-23) is a pivotal factor in the development of psoriasis, and icotrokinra is a new oral IL-23 receptor antagonist that has shown potential effectiveness in clinical trials. The main goal of this systematic review and meta-analysis was to assess the effectiveness and safety of icotrokinra in adults and adolescents with moderate-to-severe plaque-type psoriasis. Methods: A comprehensive literature search in PubMed, ScienceDirect, and the Cochrane Library, conducted in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) standards, identified randomized controlled trials that evaluated daily oral icotrokinra 200 mg versus placebo. The primary outcomes were Psoriasis Area and Severity Index (PASI) 90, Investigator's Global Assessment (IGA) 0/1, and adverse events (AEs) at 16 weeks. Risk ratios with 95% confidence intervals were summed up through a random-effects model. Results: A total of five randomized controlled trials involving 2,755 participants were included. Icotrokinra showed a significant increase in PASI 90, IGA 0/1, IGA 0, and Psoriasis Symptoms and Signs Diary 0 responses compared to placebo. The overall frequency of AEs was similar in both groups, but the rate of treatment discontinuation due to AEs was lower with icotrokinra. Conclusions: Icotrokinra is an effective and well-tolerated oral treatment for moderate-to-severe plaque psoriasis with considerable clinical and patient-reported benefits.

Indexed as

icotrokinraIL-23 inhibitorinterleukin-23meta-analysisPASI-90plaque psoriasisPsoriasis Area and Severity Indexsystematic review

Identifiers

PMID42840331
PMCPMC13639414

What OpenQuestion holds

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Registered trials

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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.