The FDA has approved their use for these purposes
About one-third of her patients who relapse after the first round will need only topical therapy consisting of a topical retinoid or topical benzoyl peroxide combination treatment
The data reviewed is a secondary analysis of existing data, does not involve intervention or interaction with human subjects, and is de-identified per the de-identification standard defined in Section 164.514(a) of the HIPAA Privacy Rule
FDA review takes 1012 months, putting approval in late 2027 or Q1 2028, with commercial launch following 13 months later
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