The purpose of this study is to evaluate the safety and tolerability of 1 mg osilodrostat therapy in patients with mild autonomous cortisol secretion (MACS), and to determine the impact on 24h urine steroid metabolome and circadian cortisol/cortisone concentrations
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Osilodrostat 1 mg administered between noon and 6 pm daily, for 4 weeks
Mayo Clinic
Rochester, Minnesota, United States
RECRUITINGAdverse Events
Number of adverse events
Time frame: 4 weeks
Adrenal insufficiency
Number of subjects to experience adrenal insufficiency, defined as combined measurements of cortisol \< 7 mcg/dL and ACTH\>60 pg/dL or single cortisol \< 5 mcg/dL
Time frame: 4 weeks
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