Acne Clinical Trial
Official title:
Administration of Oral Extended Release Minocycline for Assessment of Skin and Plasma Concentrations of Minocycline
The primary objective of this study is to evaluate the skin and plasma concentrations of minocycline in subjects undergoing treatment of acne vulgaris with oral extended release minocycline. Acne lesion counts and safety/tolerance of the treatment will also be evaluated.
This will be an open label, non randomized, interventional pilot study evaluating the plasma
and skin levels of minocycline in 10 subjects with moderate to severe acne vulgaris.
Subjects with non inflammatory acne of nodular acne will not be enrolled. Subjects will be
on an oral extended release minocycline regimen of up to 2mg/kg once a day for 4 weeks.
Steady state levels of minocycline in plasma and skin will be determined.
;
Endpoint Classification: Bio-availability Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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