Corcept Therapeutics Presents Momentum Trial Data
Corcept Therapeutics presented late-breaking data from its Momentum trial examining the prevalence of endogenous hypercortisolism in patients with resistant hypertension at the 2026 American College of Cardiology Annual Scientific Session, ACC 2026. Momentum screened 1,086 patients with resistant hypertension and found that 27.3 percent, or 297 patients had hypercortisolism. This finding complements the results of Corcept's Catalyst trial, which found hypercortisolism in 23.8 percent of the 1,057 patients screened with difficult-to-control type 2 diabetes. The prevalence of hypercortisolism in patients who had hemoglobin A1c of 7.5 percent or higher and were taking 3 or more blood pressure medicines was 32.6 percent in Momentum and 36.6 percent in Catalyst.
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- Lawsuit Timeline: Rosen Law Firm reminds investors who purchased Corcept (NASDAQ:CORT) common stock between October 31, 2024, and December 30, 2025, that they must apply to be lead plaintiff by April 21, 2026, to participate in the class action and seek compensation.
- Fee Arrangement: Investors joining the class action will not incur any upfront costs, as the law firm will operate on a contingency fee basis, thereby reducing the financial burden on investors.
- Case Background: The lawsuit alleges that Corcept made false statements regarding the support for its drug relacorilant's New Drug Application (NDA) to the FDA, claiming strong clinical trial backing, while the FDA had raised concerns about the adequacy of clinical evidence, exposing investors to potential losses.
- Law Firm's Strength: Rosen Law Firm specializes in securities class actions and recovered over $438 million for investors in 2019 alone, being ranked first in 2017 for the number of securities class action settlements, demonstrating its expertise and success in this field.
- Class Action Filed: Pomerantz LLP has announced a class action lawsuit against Corcept Therapeutics, alleging securities fraud and other unlawful business practices, with investors required to apply as Lead Plaintiff by April 21, 2026.
- FDA's Negative Response: On December 31, 2025, Corcept received a Complete Response Letter from the FDA, which requested additional evidence of effectiveness for relacorilant, indicating significant concerns regarding the drug's safety and efficacy from the regulatory body.
- Stock Price Plunge: Following the FDA's announcement, Corcept's stock price plummeted by $35.40, a 50.4% drop, closing at $34.80 per share, reflecting the market's pessimistic outlook on the company's future prospects.
- Legal Firm Background: Pomerantz LLP is a prominent class action law firm specializing in securities and antitrust litigation, with a long history of recovering multimillion-dollar damages for victims, demonstrating its strong capabilities in the legal field.
- Lawsuit Timeline: Investors who purchased Corcept Therapeutics (NASDAQ: CORT) common stock between October 31, 2024, and December 30, 2025, should note that the deadline to apply as lead plaintiff is April 21, 2026, after which they will lose their right to participate.
- Fee Arrangement: Investors joining the Corcept class action will incur no out-of-pocket expenses, as attorney fees will be covered through a contingency fee arrangement, thereby reducing financial burdens and encouraging broader participation in the lawsuit.
- Law Firm Background: The Rosen Law Firm specializes in securities class actions and has recovered over $438 million for investors in 2019 alone, demonstrating its strong track record and expertise, which investors should consider when selecting legal counsel.
- FDA Regulatory Risks: The lawsuit alleges that Corcept misrepresented the clinical trial support for its relacorilant NDA, leading to investor losses when the truth emerged, highlighting significant risks and uncertainties in the company's drug approval process.
- Lawsuit Reminder: The Schall Law Firm alerts investors of a class action lawsuit against Corcept Therapeutics (NASDAQ:CORT) for violations of §§10(b) and 20(a) of the Securities Exchange Act, concerning securities purchased between October 31, 2024, and December 30, 2025.
- False Statements: The complaint alleges that Corcept made false and misleading statements regarding the viability of its product candidate, relacorilant, claiming it was 'approaching approval' while knowing the FDA deemed its clinical data inadequate for approval.
- Investor Losses: When the market learned the truth about Corcept, investors suffered damages, indicating that the company's public statements were false and materially misleading throughout the class period.
- Legal Consultation Opportunity: The Schall Law Firm encourages investors who purchased Corcept securities during the class period to contact them before April 21, 2026, to discuss their rights and participate in the lawsuit to seek compensation for their losses.
- Class Action Notice: Rosen Law Firm reminds investors who purchased Corcept Therapeutics (NASDAQ: CORT) common stock between October 31, 2024, and December 30, 2025, to apply as lead plaintiffs by April 21, 2026, to participate in the class action and seek compensation.
- Lawsuit Background: The lawsuit alleges that Corcept made false statements regarding the strong support from FDA for the NDA of relacorilant, while in reality, the FDA had raised concerns about the adequacy of clinical evidence, exposing investors to significant risks.
- Law Firm's Strength: Rosen Law Firm specializes in securities class actions, having recovered over $438 million for investors in 2019 alone, and was ranked No. 1 by ISS Securities Class Action Services in 2017, showcasing its strong capabilities and successful track record in this field.
- Investor Action Advice: Investors can visit Rosen Law Firm's website or call the toll-free number for more information, emphasizing the importance of selecting qualified legal counsel to ensure optimal representation in the lawsuit and avoid inexperienced intermediaries.
- Study Overview: At the 2026 American College of Cardiology Annual Scientific Session (ACC 2026), Corcept Therapeutics presented data from the MOMENTUM trial, revealing that 27.3% (297 patients) of 1,086 individuals with resistant hypertension were found to have endogenous hypercortisolism, providing new insights for personalized treatment of hypertension.
- Diabetes Correlation: The findings from MOMENTUM complement those of the CATALYST trial, which identified hypercortisolism in 23.8% of 1,057 patients with difficult-to-control type 2 diabetes, indicating a higher prevalence of hypercortisolism in patients with elevated blood sugar and underscoring the importance of screening these individuals.
- Clinical Significance: The research indicates that hypercortisolism's prevalence among resistant hypertension patients may increase the risk of cardiovascular events such as heart attacks and strokes, highlighting the necessity for screening to provide more personalized medical care for these challenging cases.
- Future Research Directions: Corcept's Chief Development Officer, Bill Guyer, noted that the prevalence of hypercortisolism is greater than previously assumed, and the company will continue to advocate for improved screening and treatment options to enhance patient quality of life and treatment outcomes.









