Evidence map›Paper›PMID 26910853›Full record

ReviewDermatology and therapy2016

Ixekizumab for the Treatment of Psoriasis: A Review of Phase III Trials.

Benjamin Farahnik, Kourosh Beroukhim, Tian Hao Zhu, Michael Abrouk, Mio Nakamura, Rasnik Singh, Kristina Lee, Tina Bhutani, John Koo

Abstract readReview
In one paragraph

Review in Dermatology and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Discovery of [1,2,4]Triazolo[1,5-ACS medicinal chemistry letters · 2020
    Article
  14. Current Developments in the Immunology of Psoriasis.The Yale journal of biology and medicine · 2020
    Review
  15. Article
  16. Review
  17. Review
  18. Cytokines in uveitis.Current opinion in ophthalmology · 2018
    Review
  19. Cutaneous Manifestations of Reactions to Biologics.Current allergy and asthma reports · 2018
    Review
  20. The Role of IL-17 in Protection against Mucosal Candida Infections.Journal of fungi (Basel, Switzerland) · 2017
    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

9 authors.

Benjamin FarahnikUniversity of Vermont College of Medicine, Burlington, VT, USA. Benjamin.farahnik@ucsf.edu.
Kourosh BeroukhimUniversity of California-Los Angeles, David Geffen School of Medicine, Los Angeles, CA, USA.
Tian Hao ZhuUniversity of Southern California Keck School of Medicine, Los Angeles, CA, USA.
Michael AbroukUniversity of California-Irvine, School of Medicine, Irvine, CA, USA.
Mio NakamuraDepartment of Dermatology, Psoriasis and Skin Treatment Center, University of California-San Francisco, San Francisco, CA, USA.
Rasnik SinghUniversity of California-Los Angeles, David Geffen School of Medicine, Los Angeles, CA, USA.
Kristina LeeDepartment of Dermatology, Psoriasis and Skin Treatment Center, University of California-San Francisco, San Francisco, CA, USA.
Tina BhutaniDepartment of Dermatology, Psoriasis and Skin Treatment Center, University of California-San Francisco, San Francisco, CA, USA.
John KooDepartment of Dermatology, Psoriasis and Skin Treatment Center, University of California-San Francisco, San Francisco, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInterleukin-17 inhibitors are the newest class of monoclonal antibodies approved by the US Food and Drug Administration for the treatment of psoriasis. Preclinical and Phase II studies of ixekizumab, a high-affinity anti-IL-17A monoclonal antibody, have proved promising.

methodsWe conducted an extensive literature search using the PubMed database to assess the efficacy and safety profile of ixekizumab. The search included the following key words: "psoriasis" and "IL-17" or "ixekizumab." We also reviewed citations within articles to identify relevant sources.

resultsBy week 12, the percentage of patients achieving a 75% improvement from baseline Psoriasis Area and Severity Index (PASI 75) was comparable among the three Phase III trials (UNCOVER-1, 89%; UNCOVER-2, 90%; UNCOVER-3, 87%). Ixekizumab continued to be efficacious through 60 weeks of treatment. The safety profile of ixekizumab was favorable; the most frequently reported adverse events consisted of nasopharyngitis, upper respiratory tract infection, injection-site reaction, and headache.

conclusionOverall, ixekizumab demonstrated rapid clinical improvement and favorable short-term safety profile in Phase III trials. The results support ixekizumab as an effective therapeutic option for patients with moderate-to-severe plaque-type psoriasis.

Indexed as

Anti-interleukin-17BiologicsInterleukin 17IxekizumabPhase IIIPsoriasisUNCOVER

Identifiers

PMID26910853
PMCPMC4799032

What OpenQuestion holds

Textmetadata
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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.