Evidence map›Paper›PMID 40071721›Full record

Trial reportThe Journal of dermatology2025

Efficacy and safety of ritlecitinib in Asian patients with alopecia areata: A subgroup analysis of the ALLEGRO phase 2b/3 trial.

Xingqi Zhang, Yanting Ye, Weiling Sun, Youyu Sheng, Misaki Kinoshita-Ise, Taisuke Ito, Cheng-Che Lan, Ohsang Kwon, Gregor Schaefer, Robert Wolk and 4 more

Abstract readClinical Trial, Phase IIRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in The Journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. 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

14 authors.

Xingqi ZhangDepartment of Dermatology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Yanting YeDepartment of Dermatology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Weiling SunThe First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Youyu ShengHuashan Hospital, Fudan University, Shanghai, China.
Misaki Kinoshita-IseKyorin University Faculty of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9440-6663
Taisuke ItoHamamatsu University School of Medicine, Hamamatsu, Japan.ORCID https://orcid.org/0000-0002-9274-7050
Cheng-Che LanDepartment of Dermatology, College of Medicine and Chung-Ho Memorial Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID https://orcid.org/0000-0003-4654-118X
Ohsang KwonSeoul National University College of Medicine, Seoul, South Korea.ORCID https://orcid.org/0000-0003-0464-5124
Gregor SchaeferPfizer Pharma GmbH, Berlin, Germany.
Robert WolkPfizer Inc, Groton, Connecticut, USA.
Shasha HuPfizer China R&D, Beijing, China.
Qiankun SunPfizer China R&D, Shanghai, China.
Yimeng ShenPfizer PBG, Beijing, China.
Masayo Sakaki-YumotoPfizer Japan Inc, Tokyo, Japan.ORCID https://orcid.org/0009-0001-8781-452X

Funding

Pfizer
6 · The paper itself

Abstract

This subgroup analysis of the ALLEGRO phase 2b/3 study (NCT3732807) assessed the efficacy and safety of multiple doses of ritlecitinib, an oral JAK3/TEC family kinase inhibitor, in Asian patients with alopecia areata (AA). Patients aged ≥12 years with AA and ≥50% scalp hair loss received once-daily ritlecitinib 50 or 30 mg (with or without 4-week 200-mg loading dose ["200/50" or "200/30"]) or 10 mg or placebo for 24 weeks, followed by a 24-week extension, in which patients initially assigned to placebo switched to 200/50 or 50 mg. In this subgroup analysis, Asian patients with response based on achieving a Severity of Alopecia Tool (SALT) score ≤20, SALT ≤10, ≥2-grade improvement or normal score on the eyebrow assessment (EBA) scale, and ≥2-grade improvement or normal score on the eyelash assessment (ELA) scale were evaluated through week 48. Safety was monitored throughout. In total, 186 Asian patients were randomized to ritlecitinib 200/50 mg (n = 33), 200/30 mg (n = 28), 50 mg (n = 43), 30 mg (n = 34), 10 mg (n = 17), placebo to 200/50 mg (n = 14), or placebo to 50 mg (n = 17). The proportions of patients treated with ritlecitinib ≥30 mg achieving a SALT score ≤20 response were 9.1%-36.4% at week 24 vs 0% for the 10-mg group and 3.2% for placebo. At week 48, 26.5%-55.6% of patients treated with ritlecitinib ≥30 mg achieved a SALT ≤20 response. At week 48, the proportions of patients treated with ritlecitinib ≥30 mg with EBA response were 41.9%-71.1% and with ELA response were 40.7%-57.9%. The most common adverse events were nasopharyngitis, folliculitis, upper respiratory tract infection, and urticaria. No serious or opportunistic infections, major adverse cardiovascular events, thromboembolic events, malignancies, or deaths were reported. Ritlecitinib demonstrated clinical efficacy and acceptable safety over 48 weeks in Asian patients ≥12 years with AA and ≥50% hair loss. Results for the Asian subpopulation were consistent with the overall population in the ALLEGRO-2b/3 study.

Indexed as

Alopecia AreataProtein Kinase InhibitorsAdolescentAdultAgedAsian PeopleDose-Response Relationship, DrugDouble-Blind MethodDrug Administration ScheduleFemaleHumansMaleMiddle AgedSeverity of Illness IndexTreatment OutcomeYoung AdultProtein Kinase InhibitorsALLEGROalopecia areataritlecitinibSALTSeverity of Alopecia Tool

Identifiers

PMID40071721
PMCPMC11975179

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.