Evidence map›Paper›PMID 35230488›Full record

Trial reportArchives of dermatological research2023

A phase 2a randomized vehicle-controlled multi-center study of the safety and efficacy of delgocitinib in subjects with moderate-to-severe alopecia areata.

Daniela Mikhaylov, Jacob W Glickman, Ester Del Duca, John Nia, Peter Hashim, Giselle K Singer, Alba L Posligua, Aleksandra G Florek, Erin Ibler, Erika L Hagstrom and 5 more

Abstract readRandomized Controlled TrialMulticenter StudyClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Archives of dermatological research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 4 pooled it
7.6field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 4 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. S3 guideline diagnostics and therapy in alopecia areata - Part 2: Therapy, psychosocial and cosmetic support.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2026
    Guideline
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. Review
  7. Review
  8. Review
  9. Alopecia areata.Nature reviews. Disease primers · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Mechanism of PPARα agonist in alopecia areata.American journal of translational research · 2025
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. JAK-STAT pathway inhibitors in dermatology.Anais brasileiros de dermatologia
    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

15 authors at 2 institutions in 2 countries.

Daniela MikhaylovLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jacob W GlickmanLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ester Del DucaLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
John NiaLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Peter HashimLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Giselle K SingerLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Alba L PosliguaDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Aleksandra G FlorekDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Erin IblerDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Erika L HagstromDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Yeriel EstradaLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Stephanie M RangelDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Maria ColavincenzoDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Amy S PallerDepartment of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Emma Guttman-YasskyLaboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA. emma.guttman@mountsinai.org.
Icahn School of Medicine at Mount Sinai · USNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alopecia areata/AA is an autoimmune cause of nonscarring hair loss. The pathogenesis of AA involves many immune axes, including Th1/Th2 pathways. Delgocitinib is a pan-Janus kinase/JAK inhibitor that broadly blocks pro-inflammatory cytokines and has been effective in other inflammatory skin conditions. Recent human studies/reports have shown that use of some systemic JAK inhibitors led to hair regrowth, suggesting this medication class as a potential therapy for AA. However, topical treatment is desirable due to potential systemic side effects. To assess the efficacy and safety of topical delgocitinib in AA, we conducted a double-blind, randomized, vehicle-controlled clinical trial in 31 moderate-to-severe AA patients that were randomized 2:1 to receive delgocitinib ointment 30 mg/g (n = 20) or ointment vehicle (n = 11) for 12 weeks. The primary endpoint was change in severity of Alopecia Tool/SALT score from baseline to week 12. The secondary endpoint included safety profile by reported adverse events. Twenty-three subjects completed the trial, with eight discontinuing mostly due to voluntary withdrawal. Ten patients receiving delgocitinib ointment and three patients receiving vehicle showed SALT score improvements after 12 weeks, but the mean percent SALT improvement at week 12 compared to baseline between the two arms was not significant (p = 0.92). Our study suggests that delgocitinib ointment is not effective in moderate-to-severe AA, likely due to its inability to penetrate sufficiently deeply into the dermis of the scalp, but larger studies are necessary to assess whether a different formulation of topical JAK inhibitors may be suitable to treat mild or more localized forms of AA.

Indexed as

Alopecia AreataJanus Kinase InhibitorsHumansOintmentsPyrrolesTreatment OutcomedelgocitinibJanus Kinase InhibitorsOintmentsPyrrolesAlopecia areataAlopecia totalisAlopecia universalisDelgocitinibJAK inhibitorModerate-to-severe AAVehicle-controlled

Identifiers

PMID35230488
OpenAlexW4214613408

What OpenQuestion holds

Textmetadata
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.