Efficacy and safety of deuruxolitinib, an oral selective Janus kinase inhibitor, in adults with alopecia areata: Results from the Phase 3 randomized, controlled trial (THRIVE-AA1).

Alopecia areata Janus kinase (JAK) inhibitor Phase 3 Severity of Alopecia Tool (SALT) THRIVE-AA1 deuruxolitinib

Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
23 Jul 2024
Historique:
received: 26 01 2024
revised: 30 05 2024
accepted: 22 06 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 25 7 2024
Statut: aheadofprint

Résumé

Alopecia areata (AA) is a hair loss disorder that can seriously impact quality of life. Janus kinase (JAK) inhibitors, including deuruxolitinib, have previously demonstrated significant hair regrowth in AA. The Phase 3 THRIVE-AA1 randomized, double-blinded, placebo-controlled trial (NCT04518995) evaluated safety and efficacy of the oral JAK1/JAK2 inhibitor deuruxolitinib in adult patients with AA. Patients aged 18-65 years with ≥50% hair loss were randomized to deuruxolitinib 8 mg BID, deuruxolitinib 12 mg BID, or placebo for 24 weeks. The primary endpoint was percentage of patients achieving Severity of Alopecia Tool (SALT) score ≤20. A key secondary endpoint was percentage of satisfaction of hair patient-reported outcome (SPRO) responders. Significantly higher proportions of patients taking deuruxolitinib met the primary endpoint (8 mg 29.6%; 12 mg 41.5% versus placebo 0.8%). Both deuruxolitinib doses achieved significant improvements in all secondary endpoints versus placebo, including SPRO (8 mg 42.1%; 12 mg 53.0% versus placebo 4.7%). Most treatment-emergent adverse events were mild or moderate, consistent with other oral JAK inhibitors. Further studies are required to understand longer-term safety, efficacy, and impact of treatment cessation. Both doses of deuruxolitinib were effective for hair regrowth. Patient satisfaction aligned with hair growth.

Sections du résumé

BACKGROUND BACKGROUND
Alopecia areata (AA) is a hair loss disorder that can seriously impact quality of life. Janus kinase (JAK) inhibitors, including deuruxolitinib, have previously demonstrated significant hair regrowth in AA.
OBJECTIVE OBJECTIVE
The Phase 3 THRIVE-AA1 randomized, double-blinded, placebo-controlled trial (NCT04518995) evaluated safety and efficacy of the oral JAK1/JAK2 inhibitor deuruxolitinib in adult patients with AA.
METHODS METHODS
Patients aged 18-65 years with ≥50% hair loss were randomized to deuruxolitinib 8 mg BID, deuruxolitinib 12 mg BID, or placebo for 24 weeks. The primary endpoint was percentage of patients achieving Severity of Alopecia Tool (SALT) score ≤20. A key secondary endpoint was percentage of satisfaction of hair patient-reported outcome (SPRO) responders.
RESULTS RESULTS
Significantly higher proportions of patients taking deuruxolitinib met the primary endpoint (8 mg 29.6%; 12 mg 41.5% versus placebo 0.8%). Both deuruxolitinib doses achieved significant improvements in all secondary endpoints versus placebo, including SPRO (8 mg 42.1%; 12 mg 53.0% versus placebo 4.7%). Most treatment-emergent adverse events were mild or moderate, consistent with other oral JAK inhibitors.
LIMITATIONS CONCLUSIONS
Further studies are required to understand longer-term safety, efficacy, and impact of treatment cessation.
CONCLUSION CONCLUSIONS
Both doses of deuruxolitinib were effective for hair regrowth. Patient satisfaction aligned with hair growth.

Identifiants

pubmed: 39053611
pii: S0190-9622(24)02550-7
doi: 10.1016/j.jaad.2024.06.097
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Brett King (B)

Department of Dermatology, Yale School of Medicine, New Haven, CT, US. Electronic address: brett.king@yale.edu.

Maryanne M Senna (MM)

Lahey Hair Loss Center of Excellence, Lahey Hospital and Medical Center, Burlington, MA, US.

Natasha A Mesinkovska (NA)

Department of Dermatology, University of California, Irvine, CA, US.

Charles Lynde (C)

Department of Medicine, University of Toronto, Toronto, ON, Canada; Lynderm Research Inc., Probity Medical Research, Markham, ON, Canada.

Matthew Zirwas (M)

DOCS Dermatology, Columbus, OH, US.

Catherine Maari (C)

Faculty of Medicine, University of Montreal, Montreal, QC, Canada.

Vimal H Prajapati (VH)

Division of Dermatology, Department of Medicine, and Sections of Community Pediatrics and Pediatric Rheumatology, Department of Pediatrics, University of Calgary, Calgary, AB, Canada; Dermatology Research Institute, Probity Medical Research, Skin Health & Wellness Centre, Calgary, AB, Canada.

Sheetal Sapra (S)

Institute of Cosmetic and Laser Surgery, Oakville, ON, Canada.

Pawel Brzewski (P)

Department of Dermatology, Jagiellonian University, Krakow, Poland.

Lawrence Osman (L)

Quest Dermatology Research, Northridge, CA, US.

Sameh Hanna (S)

Department of Medicine, Division of Dermatology, University of Toronto, ON, Canada; Dermatology On Bloor, Toronto, ON, Canada.

Marni C Wiseman (MC)

Section of Dermatology, Department of Medicine, University of Manitoba, Winnipeg, MB, Canada.

Colleen Hamilton (C)

Sun Pharmaceutical Industries, Inc., Lexington, MA, US.

James Cassella (J)

Sun Pharmaceutical Industries, Inc., Lexington, MA, US.

Classifications MeSH