10-Q · July 29, 2026
Corcept delivered a strong Q2 recovery, with revenue rising 31.7% year over year to $256.147 million and diluted EPS increasing to $0.36 from $0.29. The April Lifyorli launch contributed $47.564 million, while the…
Earnings analysis · 10-Q
Filed November 3, 2026 · Our reading of the company's report
The latest report
Corcept delivered strong third-quarter execution, with revenue of $340.5 million and diluted EPS of $1.01, both materially above the prior quarter and prior-year quarter. Growth was led in part by Lifyorli revenue of…
Corcept delivered strong third-quarter execution, with revenue of $340.5 million and diluted EPS of $1.01, both materially above the prior quarter and prior-year quarter. Growth was led in part by Lifyorli revenue of $91.4 million, up 92% year over year, while cash and investments reached $662.3 million. The company maintained its 2026 revenue outlook of $1.1 billion to $1.2 billion, but pending relacorilant regulatory decisions, generic pricing pressure, and multiple legal proceedings limit the overall risk-adjusted outlook.
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Third-quarter revenue was $340.5 million, up approximately 33% from $256 million in the prior quarter and approximately 64% from $208 million in the prior-year quarter.
Diluted EPS was $1.01, compared with $0.36 in the prior quarter and $0.16 in the prior-year quarter, representing increases of approximately 181% and 531%, respectively.
Lifyorli revenue reached $91.4 million, increasing 92% year over year and providing a significant growth contribution.
Cash and investments reached $662.3 million, providing substantial liquidity to fund commercial activities and development programs.
The company maintained 2026 revenue guidance of $1.1 billion to $1.2 billion, despite pending regulatory decisions and pricing pressure from generic competition.
The FDA assigned a December 17, 2026 PDUFA target date for the resubmitted relacorilant NDA, while the European Commission is expected to issue a final decision on the MAA in the fourth quarter of 2026; either decision could be delayed or unfavorable.
Teva launched a generic version of Korlym in January 2024, and the company states that the generic has materially reduced the price received for its hypercortisolism products; Sun and Hikma may also launch products if FDA approval is obtained and Teva remains commercially available.
The Teva antitrust litigation is scheduled for summary-judgment hearing on December 16, 2026 and trial in March 2027; the company also faces a securities class action covering October 31, 2024 through December 30, 2025 and a qui tam action filed in 2017.
The proposed GUARD pricing model could impose additional rebates on qualifying Medicare Part D drugs for 25% of beneficiaries from January 1, 2027 through December 31, 2031, potentially reducing Lifyorli revenue.
The company relies on Curant to collect payments from insurers representing more than 99% of hypercortisolism revenue; operational or compliance problems at Curant could disrupt dispensing and collections.
2026 revenue guidance was reiterated at $1.1 billion to $1.2 billion; no quantitative EPS guidance was provided.
Corcept delivered a strong Q2 recovery, with revenue rising 31.7% year over year to $256.147 million and diluted EPS increasing to $0.36 from $0.29. The April Lifyorli launch contributed $47.564 million, while the…
Corcept Therapeutics reported weaker-than-expected financials for Q1 2026, with revenues of $164.9 million falling short of the $183.8 million consensus estimate, leading to a diluted EPS of -$0.30 compared to an…
Corcept’s 2025 10-K shows a company at a clinical inflection point: strong oncology data (ROSELLA: 30% reduction in progression risk, HR 0.70, and 35% reduction in death, HR 0.65; median OS 16.0 vs 11.9 months) and an…
Corcept reported Q3 product revenue of $207,638 (in thousands), up $25,092 vs. Q3 2024, but operating income compressed to $10,219 (in thousands) as SG&A and R&D rose. Diluted EPS was $0.16 for the quarter. Liquidity…
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