2019
DOI: 10.1016/j.jaad.2018.07.016
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Lightening Becker nevus with topical glycolic acid

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Cited by 11 publications
(6 citation statements)
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“…IXORA-S was a 52-week, phase 3b, multicentre, randomised, double-blind, head-to-head trial in which eligible patients with moderate-to-severe plaque psoriasis were randomised (1:1) to receive either IXE (160-mg starting dose administered as two 80-mg injections, then 80 mg every 2 weeks for 12 weeks followed by 80 mg every 4 weeks; N = 136) or UST (45-mg/90-mg weight-based dosing at weeks 0, 4 and every 12 weeks thereafter per label; N = 166) [ 20 , 21 ]. No concomitant psoriasis treatments were allowed during the trial.…”
Section: Methodsmentioning
confidence: 99%
“…IXORA-S was a 52-week, phase 3b, multicentre, randomised, double-blind, head-to-head trial in which eligible patients with moderate-to-severe plaque psoriasis were randomised (1:1) to receive either IXE (160-mg starting dose administered as two 80-mg injections, then 80 mg every 2 weeks for 12 weeks followed by 80 mg every 4 weeks; N = 136) or UST (45-mg/90-mg weight-based dosing at weeks 0, 4 and every 12 weeks thereafter per label; N = 166) [ 20 , 21 ]. No concomitant psoriasis treatments were allowed during the trial.…”
Section: Methodsmentioning
confidence: 99%
“…The 30‐week treatment did not have a better effect than the 8‐week treatment, but the patient was not followed up for longer 17 . Zhong reported that topical application of 70% glycolic acid solution could reduce the hyperpigmentation of BN, without any recurrence during 3 months of follow‐up 24 …”
Section: Treatment For Bnmentioning
confidence: 98%
“…17 Zhong reported that topical application of 70% glycolic acid solution could reduce the hyperpigmentation of BN, without any recurrence during 3 months of follow-up. 24…”
Section: Topical Therapymentioning
confidence: 99%
“…Tapinarof (GSK2894512) is a naturally derived stilbene particle that activates AhR, subsequently inducing the expression of barrier genes in keratinocytes and downregulating the Th 17 pathway, thereby possessing the potential for alleviating symptoms of AD [ 211 ]. In a recent phase II study, 247 patients with AD were randomized to receive tapinar of cream or vehicle for 12 weeks [ 213 ]. In addition to achieving improvement in terms of the Investigator’s Global Assessment (IGA) and Eczema Area and Severity Index (EASI), pruritus also improved (according to NRS), with differences between the active and vehicle arms beginning to unveil at week 2.…”
Section: Aryl Hydrocarbon Receptor Agonistsmentioning
confidence: 99%