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ArticleDermatology and therapy2026

Efficacy of Apremilast in Patients with Psoriasis with Limited Skin Involvement, Including High-Impact Site Involvement: A Pooled Analysis of Six Trials.

Bruce Strober, Mark Lebwohl, Peter van de Kerkhof, Linda Stein Gold, Joseph F Merola, Yukari Okubo, Paolo Gisondi, Zhenwei Zhou, Siddharth Chaudhari, Cynthia Deignan and 1 more

6 registry-linked trialsAbstract read
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In one paragraph

Article in Dermatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 6 registered trials, which are not on this 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.

NCT02425826 phase4completednot on this map

A Phase 4, Multicenter, Randomized, Placebo-controlled, Double-blind, Study of the Efficacy and Safety of Apremilast (CC-10004) in Subjects With Moderate Plaque Psoriasis

TypeinterventionalSponsorAmgenRan2015 to 2016Enrolled221ConditionsParapsoriasisArmsApremilast, Placebo, Placebo-Apremilast
NCT03123471 phase3completednot on this map

A Phase 3, Multi-Center, Randomized, Placebo-Controlled, Double-Blind, Study of the Efficacy and Safety of Apremilast (CC-10004) in Subjects With Moderate to Severe Plaque Psoriasis of the Scalp

TypeinterventionalSponsorAmgenRan2017 to 2019Enrolled303ConditionsPsoriasisArmsApremilast, Placebo
NCT03721172 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Placebo-Controlled, Double-Blind Study of the Efficacy and Safety of Apremilast (CC-10004) in Subjects With Mild to Moderate Plaque Psoriasis

TypeinterventionalSponsorAmgenRan2019 to 2020Enrolled595ConditionsPsoriasisArmsApremilast, Placebo
NCT03774875 phase4completednot on this map

A Phase 4, Multi-center, Randomized, Double-blind, Placebo-controlled Study of the Impact of Apremilast (CC-10004) on Quality of Life, Efficacy, and Safety in Subjects With Manifestations of Plaque Psoriasis and Impaired Quality of Life

TypeinterventionalSponsorAmgenRan2019 to 2021Enrolled277ConditionsPsoriasisArmsApremilast, Placebo
NCT03777436 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Placebo-Controlled, Double Blind-Study of the Efficacy and Safety of Apremilast (CC-10004) in Subjects With Moderate to Severe Genital Psoriasis

TypeinterventionalSponsorAmgenRan2019 to 2022Enrolled289ConditionsPsoriasisArmsApremilast, Placebo
NCT03930186 phase3completednot on this map

A Phase 3b, Open-label, Single-arm Study of the Efficacy and Safety of Apremilast, in Subjects With Plaque Psoriasis That is Not Adequately Controlled by Topical Therapy

TypeinterventionalSponsorAmgenRan2019 to 2020Enrolled152ConditionsPlaque PsoriasisArmsApremilast, Topical Therapy
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

11 authors.

Bruce StroberYale School of Medicine, New Haven, CT, USA. brucestrober30@me.com.ORCID http://orcid.org/0000-0002-8394-2057
Mark LebwohlIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Peter van de KerkhofDepartment of Dermatology, Radboud University Medical Center, Nijmegen, The Netherlands.
Linda Stein GoldHenry Ford Health System, West Bloomfield, MI, USA.
Joseph F MerolaDepartment of Dermatology and Department of Medicine, Division of Rheumatology, UT Southwestern Medical Center, Dallas, TX, USA.
Yukari OkuboTokyo Medical University, Chome-7-1, Nishi-Shinjuku, Shinjuku, Tokyo, Japan.
Paolo GisondiUniversity Hospital of Verona, Verona, Italy.
Zhenwei ZhouAmgen Inc., Thousand Oaks, CA, USA.
Siddharth ChaudhariAmgen Inc., Thousand Oaks, CA, USA.
Cynthia DeignanAmgen Inc., Thousand Oaks, CA, USA.
Ulrich MrowietzPsoriasis Center at the Department of Dermatology, University Medical Center Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPlaque psoriasis is associated with decreased quality of life (QOL) even in patients with limited skin involvement, particularly those with high-impact site (HIS) involvement. The efficacy of apremilast in patients with plaque psoriasis has been demonstrated in phase 3 and 4 clinical trials. Here, we evaluated the efficacy of apremilast across six clinical trials for patients with psoriasis with low affected body surface area (BSA), including patients with HIS involvement.

methodsData were pooled across five randomized, double-blind, placebo-controlled trials (patients were randomized to apremilast or placebo until week 16, followed by open-label apremilast) and one single-arm, open-label trial of apremilast for the treatment of plaque psoriasis. Patients in this post hoc pooled analysis had limited skin involvement (BSA, 3-10%), many with HIS involvement in the scalp, genital area, and/or nails. Week 16 and 32 assessments included BSA, Psoriasis Area and Severity Index (PASI), static Physician's Global Assessment, Dermatology Life Quality Index, and HIS-specific measurements. Nonresponder imputation was used for missing data for binary endpoints; a mixed-effects model for repeated measures was used to analyze continuous endpoints.

resultsOf 1152 patients in this analysis (mean BSA, 6.3%; PASI, 6.8), those who received apremilast (n = 671) versus placebo (n = 481) had significantly greater improvements in skin clearance and QOL at week 16 (all endpoints assessed, p < 0.0001), with improvements generally maintained at week 32. Apremilast also yielded clinically greater improvements in patients with scalp, genital, and/or nail psoriasis at week 16 versus placebo (all endpoints assessed in affected patients, p < 0.01), with responses generally maintained at week 32.

conclusionApremilast improved skin clearance and QOL at week 16, and responses were generally maintained at week 32, in a pooled population of patients with psoriasis with limited skin involvement, including HIS involvement. Graphical abstract available for this article. Trial Registration ClinicalTrials.gov identifiers-NCT03721172, NCT03777436, NCT03123471, NCT03774875, NCT02425826, and NCT03930186.

Indexed as

ApremilastHigh-impact siteLimited skin involvementPlaque psoriasisPooled analysisSystemic therapy

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.