Abstract | PURPOSE:
Acne vulgaris is very common among adolescents and young adults. It is important for clinicians who provide care to these patients to have a plan of action for assessing and managing acne in daily practice. METHODS: Post-hoc analysis of two large-scale phase 3 pivotal trials of trifarotene 0.005% cream, focusing on efficacy, safety, and tolerability in the subgroup of subjects aged 12 to 17, inclusive. RESULTS:
Trifarotene was effective and well tolerated on both the face and trunk in patients ages 12-17 with moderate acne. There was a low and acceptable rate of adverse events and tolerability was favorable. CONCLUSIONS:
Trifarotene monotherapy was associated with good clinical efficacy, safety, and tolerability. Once-daily application offers convenience for patients, and the low concentration of trifarotene makes it well-suited to use on large skin areas such as the trunk. J Drugs Dermatol. 2022;21(6):582-586. doi:10.36849/JDD.6778.
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Authors | Lawrence Eichenfield, Pearl Kwong, Stephanie Lee, Daniel Krowchuk, Krysten Arekapudi, Adelaide Hebert |
Journal | Journal of drugs in dermatology : JDD
(J Drugs Dermatol)
Vol. 21
Issue 6
Pg. 582-586
(Jun 01 2022)
ISSN: 1545-9616 [Print] United States |
PMID | 35674762
(Publication Type: Journal Article, Meta-Analysis)
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Chemical References |
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Topics |
- Acne Vulgaris
(drug therapy)
- Adolescent
- Child
- Clinical Trials, Phase III as Topic
- Humans
- Retinoids
(administration & dosage, adverse effects)
- Skin Cream
(administration & dosage, adverse effects)
- Treatment Outcome
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