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Corcept Therapeutics (CORT) investor relations material
Corcept Therapeutics Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Q1 2026 revenue reached $164.9 million, up 4.9% year-over-year, driven by strong endocrinology demand and new product launches, though offset by lower average price due to increased generic sales.
Net loss of $31.8 million in Q1 2026, compared to net income of $20.5 million in Q1 2025, reflecting higher operating expenses for new product launches and growth initiatives.
FDA approved Lifyorli (relacorilant) for platinum-resistant ovarian cancer in March 2026, with rapid physician adoption, NCCN guideline inclusion, and U.S. sales beginning in April.
Landmark clinical trials (CATALYST, MOMENTUM, ROSELLA) and multiple late-stage programs in oncology, MASH, and ALS are driving increased screening, treatment, and long-term growth, with key data readouts expected by year-end and into next year.
Specialty pharmacy transition to Curant Health completed in early 2026, supporting record patient starts and prescription volume.
Financial highlights
Q1 2026 revenue: $164.9 million, up from $157.2 million in Q1 2025 (4.9% growth).
Net loss: $31.8 million in Q1 2026 vs. net income of $20.5 million in Q1 2025.
Operating expenses increased to $214.5 million from $153.8 million, mainly due to launch preparations and investments.
Cash and investments totaled $515.4 million as of March 31, 2026.
R&D expenses rose to $66.3 million from $60.7 million year-over-year.
Outlook and guidance
2026 revenue guidance raised to $950–$1,050 million, reflecting confidence in endocrinology and oncology businesses.
Expect higher R&D and SG&A expenses in 2026 as clinical programs and commercialization expand.
Sufficient liquidity to fund operations and planned R&D for at least the next 12 months without additional financing.
Anticipate EMA approval for relacorilant plus nab-paclitaxel in ovarian cancer by year-end.
Results from key clinical trials (BELLA, MONARCH, ALS Phase 3) expected by end of 2026 or early 2027.
- Proxy seeks approval for director elections, auditor, executive pay, and equity plan amendment.CORT
Proxy filing17 Apr 2026 - 2025 revenue rose 13% to $761.4M, with strong Cushing's demand and advancing clinical pipeline.CORT
Q4 20259 Apr 2026 - Q2 revenue up 39% to $163.8M, guidance raised, and key clinical milestones expected by year-end.CORT
Q2 20242 Feb 2026 - Q3 revenue up 48% year-over-year, relacorilant NDA submission on track, guidance raised.CORT
Q3 202417 Jan 2026 - Q1 revenue up 7% to $157.2M; net income down; 2025 guidance held as pipeline advances.CORT
Q1 202524 Dec 2025 - 2024 revenue up 40% to $675M; relacorilant NDA submitted; 2025 guidance $900–$950M.CORT
Q4 202423 Dec 2025 - Director elections, auditor ratification, and executive pay are key 2025 meeting items.CORT
Proxy Filing1 Dec 2025 - Q2 revenue up 19% to $194.4M; net income steady; clinical and regulatory progress continues.CORT
Q2 202516 Nov 2025 - Q3 revenue up 13.8% to $207.6M; relacorilant NDAs under FDA review; net income declined.CORT
Q3 20256 Nov 2025
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