Glycopyrronium tosylate in pediatric primary axillary hyperhidrosis: Post hoc analysis of efficacy and safety findings by age from two phase three randomized controlled trials.


Journal

Pediatric dermatology
ISSN: 1525-1470
Titre abrégé: Pediatr Dermatol
Pays: United States
ID NLM: 8406799

Informations de publication

Date de publication:
Jan 2019
Historique:
pubmed: 20 11 2018
medline: 9 2 2019
entrez: 20 11 2018
Statut: ppublish

Résumé

Hyperhidrosis in pediatric patients has been understudied. Post hoc analyses of two phase 3 randomized, vehicle-controlled, 4-week trials (ATMOS-1 [NCT02530281] and ATMOS-2 [NCT02530294]) were performed to assess efficacy and safety of topical anticholinergic glycopyrronium tosylate (GT) in pediatric patients. Patients had primary axillary hyperhidrosis ≥ 6 months, average Axillary Sweating Daily Diary (ASDD/ASDD-Children [ASDD-C]) Item 2 (sweating severity) score ≥ 4, sweat production ≥ 50 mg/5 min (each axilla), and Hyperhidrosis Disease Severity Scale (HDSS) ≥ 3. Coprimary end points were ≥ 4-point improvement on ASDD/ASDD-C Item 2 (a validated patient-reported outcome) and change in gravimetrically measured sweat production at Week 4. Efficacy and safety data are shown through Week 4 for the pediatric (≥ 9 to ≤ 16 years) vs older (> 16 years) subgroups. Six hundred and ninety-seven patients were randomized in ATMOS-1/ATMOS-2 (GT, N = 463; vehicle, N = 234); 44 were ≥ 9 to ≤ 16 years (GT, n = 25; vehicle, n = 19). Baseline disease characteristics were generally similar across subgroups. GT-treated pediatric vs older patients had comparable improvements in ASDD/ASDD-C Item 2 (sweating severity) responder rate, HDSS responder rate (≥ 2-grade improvement]), sweat production, and quality of life (mean change from Baseline in Dermatology Life Quality Index [DLQI]/children's DLQI), with greater improvement vs vehicle. Treatment-emergent adverse events were similar between subgroups, and most were mild, transient, and infrequently led to discontinuation. Topical, once-daily GT improved disease severity (ASDD/ASDD-C, HDSS), sweat production, and quality of life (DLQI), with similar findings in children, adults, and the pooled population. GT was well tolerated, and treatment-emergent adverse events were qualitatively similar between subgroups and consistent with other anticholinergics.

Identifiants

pubmed: 30451318
doi: 10.1111/pde.13723
pmc: PMC6587744
doi:

Substances chimiques

Muscarinic Antagonists 0
Glycopyrrolate V92SO9WP2I

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

89-99

Subventions

Organisme : Dermira, Inc.

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2018 The Authors. Pediatric Dermatology Published by Wiley Periodicals, Inc.

Références

Pharmacol Toxicol. 1998 Sep;83(3):132-4
pubmed: 9783332
Clin Exp Dermatol. 1994 May;19(3):210-6
pubmed: 8033378
Pediatr Dermatol. 2018 Mar;35(2):208-212
pubmed: 29334132
J Drugs Dermatol. 2018 Apr 1;17(4):392-396
pubmed: 29601615
Isr J Psychiatry Relat Sci. 2000;37(1):25-31
pubmed: 10857268
Dermatol Surg. 2007 Aug;33(8):908-23
pubmed: 17661933
J Am Acad Dermatol. 2004 Aug;51(2):241-8
pubmed: 15280843
Pediatr Dermatol. 2008 Nov-Dec;25(6):591-8
pubmed: 19067862
Am J Clin Dermatol. 2019 Feb;20(1):135-145
pubmed: 30378087
Acta Derm Venereol. 2018 Jan 12;98(1):103-107
pubmed: 28761964
Rev Urol. 2003;5 Suppl 8:S26-30
pubmed: 16985986
Arch Dermatol Res. 2012 Nov;304(9):707-17
pubmed: 22843024
Pediatr Dermatol. 2019 Jan;36(1):89-99
pubmed: 30451318
Dermatol Ther (Heidelb). 2017 Mar;7(1):25-36
pubmed: 27787745
J Eur Acad Dermatol Venereol. 2013 Mar;27(3):e282-8
pubmed: 22827710
Dermatol Clin. 2014 Oct;32(4):477-84
pubmed: 25152340
Qual Life Res. 1999 Dec;8(8):693-8
pubmed: 10855343
J Am Acad Dermatol. 2019 Jan;80(1):128-138.e2
pubmed: 30003988
Arch Dermatol Res. 2016 Dec;308(10):743-749
pubmed: 27744497
J Patient Rep Outcomes. 2019 Sep 5;3(1):59
pubmed: 31486951
Int J Clin Pharmacol Ther. 2012 Jun;50(6):434-7
pubmed: 22677304
Health Qual Life Outcomes. 2006 Oct 11;4:79
pubmed: 17034633
Skin Res Technol. 2008 May;14(2):213-9
pubmed: 18412565

Auteurs

Adelaide A Hebert (AA)

UTHealth McGovern Medical School, Houston, Texas.

Dee Anna Glaser (DA)

Saint Louis University, St. Louis, Missouri.

Lawrence Green (L)

George Washington University School of Medicine, Washington, District of Columbia.

William P Werschler (WP)

Premier Clinical Research, Spokane, Washington.

Douglass W Forsha (DW)

Jordan Valley Dermatology and Research Center, West Jordan, Utah.

Janice Drew (J)

Dermira, Inc., Menlo Park, California.

Ramanan Gopalan (R)

Dermira, Inc., Menlo Park, California.

David M Pariser (DM)

Eastern Virginia Medical School and Virginia Clinical Research, Inc., Norfolk, Virginia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH