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Case Reports
. 2025 Jan 20:18:161-167.
doi: 10.2147/CCID.S498879. eCollection 2025.

Real-World Experience of Clascoterone Cream 1% in Acne Management: Case Series and Canadian Experience

Affiliations
Case Reports

Real-World Experience of Clascoterone Cream 1% in Acne Management: Case Series and Canadian Experience

Elena Tay et al. Clin Cosmet Investig Dermatol. .

Abstract

Acne vulgaris is a globally prevalent dermatological condition associated with substantial physical and psychological burden. Although acne typically presents during adolescence, it is a chronic condition that also affects many adults. Despite the spectrum of treatments available for acne, limitations in tolerability and safety concerns can present challenges for the use of conventional medications in clinical practice. Clascoterone cream 1%, a topical androgen receptor inhibitor, was recently approved in Canada for the topical treatment of acne vulgaris. This case series included 10 patients with acne vulgaris who were treated with clascoterone cream 1% as monotherapy or part of a combination treatment program between August 2023 and May 2024. Clascoterone cream 1% was effective and well tolerated regardless of acne severity, age, gender, and ethnicity. Clascoterone led to clinical improvement when used as monotherapy, adjunctive treatment in combination with other topical or systemic agents or laser therapy, and as maintenance therapy to prevent relapse of acne. Moreover, clascoterone also helped to address other concerns in several patients, including hirsutism, hidradenitis suppurativa, retinoid-induced dermatitis, androgenetic alopecia, folliculitis, postinflammatory hyperpigmentation, and laser-induced acne flares. This early real-world clinical experience supports the effectiveness, tolerability, and versatility of clascoterone cream 1% for patients with acne across a variety of clinical and demographic characteristics.

Keywords: androgen; efficacy; safety; therapy; tolerability; topical.

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Conflict of interest statement

WJL has served as an investigator, speaker, adviser/consultant, and/or received grants/honoraria from AbbVie, Allakos, Alumis, Amgen, AnaptysBio, Arcutis Biotherapeutics, Aslan, Bausch Health, BioJamp, Bristol Myers Squibb, Celgene Corporation, Celltrion, Concert Pharmaceuticals, Eli Lilly, Galderma, GSK, Incyte, Inmagene, Janssen, LEO Pharma, Medexus, Meiji Seika Pharma, Novartis, Numab, Pediapharm, Pfizer, Reistone, Sanofi, SkinCeuticals, Sun Pharma, Takeda, UCB, and Valeant. The authors report no other conflicts of interest in this work.

References

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