Difficult-to-control Type 2 diabetes (T2D)* may be in the clutches of Hypercortisolism

Hypercortisolism.

Ease the grip with Korlym

View Efficacy & Safety

In the CATALYST study, endogenous hypercortisolism was identified in 24% (252/1057) of patients with difficult-to-control T2D—and Korlym significantly reduced HbA1c in many of these patients.1,2*

Twenty-four percent.

Explore the Korlym results in eligible patients with hypercortisolism and difficult-to-control T2D

Clinical study results from the pivotal trial3,4

See Korlym's effects on glucose control and HbA1c in the SEISMIC study

View SEISMIC data
HbA1c.
Clinical study results in patients with difficult-to-control T2D2

See Korlym's effects on HbA1c and T2D medications in the CATALYST study

View CATALYST data
Study safety results2-4

See safety results from both SEISMIC and CATALYST, including commonly occurring adverse events

View safety data

*CATALYST was a prospective, phase 4 study with two parts. The first part (Screening Phase) assessed the prevalence of endogenous hypercortisolism in 1057 patients with difficult-to-control T2D diagnosed ≥1 year prior and defined as HbA1c 7.5%-11.5% AND taking ≥3 T2D medications OR insulin and other T2D medication(s) OR ≥2 T2D medications AND the presence of ≥1 microvascular or macrovascular complication AND/OR concomitant hypertension requiring ≥2 hypertension medications.  Hypercortisolism was defined as a post 1-mg DST cortisol >1.8 μg/dL with AM dexamethasone ≥140 ng/dL. In the second part (Treatment Phase), patients with hypercortisolism who met inclusion/exclusion criteria (n=136) were randomized (2:1) to receive either Korlym or placebo for 24 weeks in a double-blind, placebo-controlled manner. The primary endpoint was the reduction of HbA1c between these groups. Please see full study design on the CATALYST Study Results page.1,5

Korlym modulates cortisol activity to preserve important physiological effects of cortisol while reducing certain negative effects of excess cortisol6

For more information about Korlym

References:
  1. Buse JB, Kahn SE, Aroda VR, et al. Prevalence of hypercortisolism in patients with difficult-to-control type 2 diabetes. Diabetes Care. 2025;48(00):1-9. doi:10.2337/dc24-2841
  2. DeFronzo RA, Fonseca V, Aroda VR, et al. Inadequately controlled type 2 diabetes and hypercortisolism: improved glycemia with mifepristone treatment. Diabetes Care. 2025;00(00):1-9. doi:10.2337/dc25-1055
  3. Fleseriu M, Biller BMK, Findling JW, et al. Mifepristone, a glucocorticoid receptor antagonist, produces clinical and metabolic benefits in patients with Cushing's syndrome. J Clin Endocrinol Metab. 2012;97(6):2039-2049. doi:10.1210/jc.2011-3350
  4. Korlym Prescribing Information. Corcept Therapeutics Incorporated.
  5. DeFronzo RA, Auchus RJ, Bancos I, et al. Study protocol for a prospective, multicentre study of hypercortisolism in patients with difficult-to-control type 2 diabetes (CATALYST): prevalence and treatment with mifepristone. BMJ Open. 2024;14(7):e081121. doi:10.1136/bmjopen-2023-081121
  6. Katznelson L, Loriaux DL, Feldman D, Braunstein GD, Schteingart DE, Gross C. Global clinical response in Cushing's syndrome patients treated with mifepristone. Clin Endocrinol (Oxf). 2014;80(4):562-569. doi:10.1111/cen.12332