INITIATING KORLYM

The recommended starting dose of Korlym is 300 mg per day1

300 mg

  • The dose of Korlym may be increased in 300-mg increments to a maximum of 1200 mg/day1

  • Increases in dose should not occur more frequently than once every 2-4 weeks based on a clinical assessment of tolerability and degree of improvement in Cushing syndrome manifestations1

  • For patients with renal impairment or mild-to-moderate hepatic impairment, no change in initial Korlym dose is required. The maximum dose should be limited to 600 mg/day1

  • If Korlym treatment is interrupted, it should be reinitiated at the lowest dose (300 mg). If treatment was interrupted because of adverse reactions, the titration should aim for a dose lower than the one that resulted in treatment interruption.

  • Most patients in the SEISMIC trial (85%) achieved an initial positive response by titrating up from 300 mg/day2

  • Strong inhibitors of CYP3A may increase exposure to mifepristone. Korlym should be used in combination with strong CYP3A inhibitors only when necessary. Refer to the full Prescribing Information for dose adjustment information of Korlym when a strong CYP3A inhibitor is added as well as other drug interactions.

References:
  1. Korlym Prescribing Information. Corcept Therapeutics Incorporated.
  2. Yuen KCJ, Williams G, Kushner H, Nguyen D. Association between mifepristone dose, efficacy, and tolerability in patients with Cushing syndrome. Endocr Pract. 2015;21(10):1087-1092. doi:10.4158/EP15760.OR