About this trial

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

Eligibility criteria

Qualifiers

Provide written informed consent

Stated willingness to comply with all study procedures and availability for the duration of the study

Age ≥ 18 years

Diagnosed with MACS

Disqualifiers

Planned alternative therapy for MACS during the study period

Current use of oral exogenous glucocorticoid therapy

Current use of opioid therapy >20 MME/day

Planned use of oral exogenous glucocorticoid therapy

Trial design

Treatments tested in this trial

  • Osilodrostat 1 MG

Treatment groups

15 Participants
are divided into 1 treatment group

Locations

1
Mayo Clinic55905, RochesterMinnesota, United States

Sponsors and collaborators

Mayo Clinic

Lead sponsor

RECORDATI GROUP

Collaborator