Corcept Therapeutics (CORT) Investor presentation summary
Event summary combining transcript, slides, and related documents.
Investor presentation summary
3 Nov, 2026Operating model and strategy
Q1–Q3 2026 revenue rose from $165M to $341M; Q3 mix was $249M Korlym and $91M Lifyorli. Cash was $662M at Q3-end; FY2026 revenue guidance is $1.1B–$1.2B.
Strategy combines a cash-generating operating model, a broad cortisol-modulation therapeutic platform and collaborative R&D.
Korlym, Lifyorli and next-generation selective cortisol modulators compete with cortisol at the glucocorticoid receptor; none bind the progesterone receptor.
Hypercortisolism and Cushing’s syndrome
Relacorilant’s pivotal Phase 3 GRACE trial met its primary endpoint; patients continuing treatment were 5.9x more likely to maintain blood-pressure response than placebo recipients.
In GRACE’s open-label phase, patients with hypertension had mean reductions of 12.6 mm Hg in SBP and 8.3 mm Hg in DBP; patients with hyperglycemia had a mean 0.7% HbA1c improvement.
GRADIENT showed placebo-adjusted improvements in blood pressure, glucose measures, weight and body composition; weight improvement was 3.9 kg at 22 weeks (p=0.0001).
Relacorilant’s resubmitted NDA has a PDUFA date of December 17, 2026; composition-of-matter patents extend to 2038, with method, formulation and manufacturing patents to 2040.
CATALYST found hypercortisolism in 24% of screened patients with resistant T2D; Korlym reduced HbA1c by 1.47% versus 0.15% with placebo over 24 weeks (p<0.001).
Oncology
Lifyorli (relacorilant) plus nab-paclitaxel was FDA-approved in March 2026 for specified platinum-resistant ovarian, fallopian tube or primary peritoneal cancer; it became a preferred NCCN regimen in April 2026.
In ROSELLA, the combination improved median PFS to 6.5 vs. 5.5 months (HR 0.70; p=0.0076) and median OS to 16.0 vs. 11.9 months (HR 0.65; p=0.0004) versus nab-paclitaxel alone.
BELLA Part A reported 7.2-month median PFS and 59% ORR overall; bevacizumab-naive patients had 8.1-month median PFS and 66% ORR.
BELLA Parts B and C, TRIDENT and STELLA are Phase 2 chemotherapy-combination studies in ovarian, endometrial, pancreatic and cervical cancers; several results are expected by year-end 2027.
Phase 2 relacorilant plus enzalutamide prostate cancer and Phase 1b nenocorilant plus nivolumab solid-tumor studies are enrolling; results are expected by year-end 2027.
Latest events from Corcept Therapeutics
- Revenue rose 64% as Lifyorli adoption accelerated and regulatory catalysts approached.CORT
Q3 2026 - Q2 revenue up 32% to $256.1M; Lifyorli launch boosts guidance to $1.1–$1.2B for 2026.CORT
Q2 2026 - Q1 revenue up 4.9% to $164.9M; net loss $31.8M; 2026 guidance raised after Lifyorli approval.CORT
Q1 2026 - Proxy seeks approval for director elections, auditor, executive pay, and equity plan amendment.CORT
Proxy filing - 2025 revenue rose 13% to $761.4M, with strong Cushing's demand and advancing clinical pipeline.CORT
Q4 2025 - Q3 revenue up 14% to $207.6M; net income fell as expenses rose; pipeline and NDAs advancing.CORT
Q3 2025 - Q3 revenue up 48% year-over-year, relacorilant NDA submission on track, guidance raised.CORT
Q3 2024 - Q2 revenue up 39% to $163.8M, guidance raised, and key clinical milestones expected by year-end.CORT
Q2 2024 - Q1 revenue up 7% to $157.2M; 2025 guidance held as clinical pipeline advances.CORT
Q1 2025