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Federal Circuit backs Teva in Corcept (CORT) Korlym generic patent dispute

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Corcept Therapeutics reported that the United States Court of Appeals for the Federal Circuit has found that Teva Pharmaceuticals’ marketing of a generic version of Korlym® does not infringe two Corcept patents covering methods of safely co‑administering Korlym with CYP3A4‑inhibiting drugs commonly used by patients with Cushing’s syndrome.

The decision affirms a prior December 2023 verdict from the Federal District Court for the District of New Jersey. Corcept’s CEO said the company is disappointed with the ruling and plans to vigorously defend its intellectual property, including evaluating options to seek further judicial review of the decision.

Positive

  • None.

Negative

  • Federal Circuit non‑infringement ruling for Teva confirms that Teva’s generic Korlym® marketing does not infringe two Corcept patents on safe co‑administration methods, affirming an earlier district court verdict and weakening this part of Corcept’s intellectual property protection around Korlym.

Insights

Federal Circuit loss weakens Korlym patent shield vs. Teva generic.

The ruling that Teva’s Korlym® generic marketing does not infringe two Corcept patents removes one layer of exclusivity protection around co‑administration methods with CYP3A4‑inhibiting drugs. It also confirms a December 2023 district court verdict, raising the bar for further legal relief.

Because the decision comes from the Federal Circuit, any next steps likely involve higher‑level judicial review, which Corcept says it is considering. The case centers on methods for safely treating Cushing’s syndrome patients using Korlym alongside certain commonly prescribed drugs, so the outcome directly touches Korlym’s competitive landscape.

Future court actions or settlements, if any, would determine how strong Corcept’s remaining Korlym‑related intellectual property is relative to generic entrants. Subsequent SEC filings or legal updates will be key to understanding how this dispute ultimately resolves.

Item 8.01 Other Events Other
Voluntary disclosure of events the company deems important to shareholders but not covered by other items.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
CORCEPT THERAPEUTICS INC false 0001088856 0001088856 2026-02-19 2026-02-19
 
 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

 

FORM 8-K

 

 

CURRENT REPORT

Pursuant to Section 13 OR 15(d)

of The Securities Exchange Act of 1934

February 19, 2026

Date of Report (date of earliest event reported)

 

 

Corcept Therapeutics Incorporated

(Exact name of registrant as specified in its charter)

 

 

 

Delaware   000-50679   77-0487658
(State or other jurisdiction
of incorporation)
 

(Commission

File Number)

  (I.R.S. Employer
Identification No.)

101 Redwood Shores Parkway, Redwood City, CA 94065

(Address of Principal Executive Offices) (Zip Code)

(650) 327-3270

Registrant’s telephone number, including area code

Not Applicable

(Former name or former address, if changed since last report.)

 

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class

 

Trading
Symbol(s)

 

Name of each exchange
on which registered

Common Stock, $0.001 par value   CORT   The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 or Rule 12b-2 of the Securities Exchange Act of 1934.

Emerging growth company 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

 
 


Item 8.01.

Other Events.

On February 19, 2026, Corcept Therapeutics Incorporated (the “Company”) issued a press release announcing that the United States Court of Appeals for the Federal Circuit has found that Teva Pharmaceuticals’ marketing of a generic version of Korlym® does not infringe two of the Company’s patents concerning methods of safely co-administering Korlym and drugs that inhibit the CYP3A4 enzyme, including drugs that are commonly prescribed to patients with Cushing’s syndrome. The press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

 

Item 9.01.

Financial Statements and Exhibits

(d) Exhibits

 

Exhibits
No.

  

Description

 99.1    Press Release of Corcept Therapeutics Incorporated, February 19, 2026.
104.1    Cover Page Interactive Data File - the cover page XBRL tags are embedded within the Inline XBRL document.


SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

    CORCEPT THERAPEUTICS INCORPORATED
Date: February 19, 2026     By:  

/s/ Atabak Mokari

    Name:   Atabak Mokari
    Title:   Chief Financial Officer

Exhibit 99.1

 

LOGO      

CONTACT:

Investor inquiries:

ir@corcept.com

Media inquiries:

communications@corcept.com

www.corcept.com

Corcept Provides Update on Patent Dispute with Teva Pharmaceuticals

REDWOOD CITY, Calif., (February 19, 2026) — Corcept Therapeutics Incorporated (NASDAQ: CORT), a commercial-stage company engaged in the discovery and development of medications to treat severe endocrinologic, oncologic, metabolic and neurologic disorders by modulating the effects of the hormone cortisol, today announced that the United States Court of Appeals for the Federal Circuit has found that Teva Pharmaceuticals’ marketing of a generic version of Korlym® does not infringe two of Corcept’s patents concerning methods of safely co-administering Korlym and drugs that inhibit the CYP3A4 enzyme, including drugs that are commonly prescribed to patients with Cushing’s syndrome. The ruling affirms a December 2023 verdict by the Federal District Court for the District of New Jersey.

“We are disappointed in the Court’s ruling,” said Joseph K. Belanoff, M.D., Corcept’s Chief Executive Officer. “The patents we asserted in this case cover methods of safely treating patients with Cushing’s syndrome that physicians rely on every day. We will vigorously defend our rights and are currently considering the best way to pursue judicial review of this decision.”

About Corcept Therapeutics

For over 25 years, Corcept has focused on cortisol modulation and its potential to treat patients with a wide variety of serious disorders and has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. Corcept is conducting advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease. In 2012, the company introduced Korlym®, the first medication approved by the U.S. Food and Drug Administration for the treatment of patients with endogenous hypercortisolism. Corcept is headquartered in Redwood City, California. For more information, visit Corcept.com.

Forward-Looking Statements

Statements in this press release, other than statements of historical fact, are forward-looking statements based on our current plans and expectations and are subject to risks and uncertainties that might cause our actual results to differ materially from those such statements express or imply. These risks and uncertainties are set forth in our SEC filings, which are available at our website and the SEC’s website. Forward-looking statements in this press release include, but are not limited to, those related to our intent to defend our intellectual property rights and our consideration of the best way to pursue judicial review of this decision. We disclaim any intention or duty to update forward-looking statements made in this press release.

FAQ

What did the Federal Circuit decide in Corcept Therapeutics (CORT) vs. Teva?

The Federal Circuit found Teva’s marketing of a generic Korlym® does not infringe two Corcept patents. Those patents cover methods of safely co‑administering Korlym with CYP3A4‑inhibiting drugs commonly used to treat patients with Cushing’s syndrome.

How does the court ruling affect Corcept Therapeutics’ Korlym patents?

The ruling determines that two Korlym‑related method patents are not infringed by Teva’s generic marketing. This narrows Corcept’s patent protection for safe co‑administration with CYP3A4 inhibitors, potentially affecting the legal barriers against generic competition for Korlym.

Did the Federal Circuit ruling in favor of Teva overturn any prior decision involving CORT?

No, the Federal Circuit ruling affirms a December 2023 verdict by the Federal District Court for the District of New Jersey. That earlier decision also found Teva’s generic Korlym® marketing did not infringe the two asserted Corcept patents involving co‑administration methods.

How did Corcept Therapeutics respond to the Federal Circuit decision on its Korlym patents?

Corcept stated it is disappointed with the ruling and emphasized that the asserted patents cover methods physicians use to safely treat Cushing’s syndrome. The company said it will vigorously defend its rights and is considering how best to seek judicial review of the decision.

Which patents were at issue in Corcept Therapeutics’ dispute with Teva over Korlym?

The dispute involved two Corcept patents covering methods of safely co‑administering Korlym® with drugs that inhibit the CYP3A4 enzyme. These drugs include medications that are commonly prescribed for patients with Cushing’s syndrome, making the patents relevant to real‑world Korlym treatment regimens.

What is Korlym and why is it important to Corcept Therapeutics (CORT)?

Korlym® is Corcept’s drug introduced in 2012 as the first FDA‑approved treatment for patients with endogenous hypercortisolism. It is central to Corcept’s cortisol‑modulation franchise, which also includes numerous proprietary selective cortisol modulators in advanced clinical trials for several serious disorders.

Filing Exhibits & Attachments

4 documents