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CORT's Q1 Earnings In Line With Estimates, Revenues Lag, Shares Fall

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Corcept Therapeutics Incorporated CORT reported first-quarter 2025 earnings of 17 cents per share, which were in line with the Zacks Consensus Estimate. The company had reported earnings of 25 cents per share in the year-ago quarter.

Revenues in the first quarter increased 7.1% year over year to $157.2 million. The figure, however, missed the Zacks Consensus Estimate of $178 million. The top line solely comprises product sales of the Cushing’s syndrome drug, Korlym. (Find the latest EPS estimates and surprises on Zacks Earnings Calendar.)

Year to date, shares of Corcept have rallied 46.8% against the industry’s decline of 0.4%.

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CORT's Q1 Earnings in Detail

Revenues from Korlym also missed our model estimate of $179.1 million.

Per management, Korlym sales in the first quarter were affected by the insufficient capacity of a specialty pharmacy vendor who was unable to fulfill the surge in demand. The lower-than-expected sales disappointed investors. Consequently, shares of CORT were down 7.5% in after-hours trading on May 5 following the earnings result announcement.

Research and development expenses rose 3.8% year over year to $60.7 million.

Selling, general and administrative expenses increased around 61.1% year over year to $90.7 million.

Consequently, operating expenses increased 31.1% year over year to $153.8 million in the first quarter.

Cash and investments, as of March 31, 2025, totaled $570.8 million compared with $603.2 million as of Dec. 31, 2024.

2025 Guidance

Corcept reiterated its total revenue guidance for 2025.

The company continues to expect total revenues in the range of $900-$950 million in 2025. The Zacks Consensus Estimate for revenues is pegged at $905.7 million.

CORT's Recent Pipeline Updates

Corcept is developing its lead candidate, relacorilant, for treating patients with Cushing’s syndrome. In December 2024, CORT submitted a new drug application (NDA) for relacorilant to the FDA for the same. The NDA was based on positive data from the GRACE study and confirmatory evidence from the phase III GRADIENT, as well as long-term extension studies and a phase II study in hypercortisolism.

In March 2025, the FDA accepted the NDA and assigned a Prescription Drug User Fee Act target action date of Dec. 30, 2025.

Corcept is also evaluating relacorilant in combination studies for treating different types of cancer indications.

The phase III ROSELLA study, which evaluated relacorilant in combination with nab-paclitaxel for treating patients with platinum-resistant ovarian cancer, met its primary endpoint of improved progression-free survival (PFS).