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[8-K] Halliburton Company Reports Material Event

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Rhea-AI Filing Summary

Corcept Therapeutics Incorporated (Nasdaq: CORT) filed a Form 8-K dated 14 July 2025 to disclose a material corporate event under Item 8.01 (Other Events).

The company has submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration for its selective cortisol modulator relacorilant to treat patients with platinum-resistant ovarian cancer. An attached press release (Exhibit 99.1) provides additional detail and is incorporated by reference. No financial results, guidance or transactional information accompanied the filing.

This NDA submission represents a significant regulatory milestone that, if approved, could diversify Corcept’s revenue base by moving the company beyond its current endocrinology focus into the oncology market. Timing of FDA review (typically 10-12 months) and eventual commercialization remain contingent on agency acceptance and approval.

Corcept Therapeutics Incorporated (Nasdaq: CORT) ha presentato un modulo Form 8-K datato 14 luglio 2025 per comunicare un evento aziendale rilevante ai sensi della voce 8.01 (Altri Eventi).

L'azienda ha inviato una New Drug Application (NDA) alla Food and Drug Administration degli Stati Uniti per il suo modulatore selettivo del cortisolo relacorilant, destinato al trattamento di pazienti con carcinoma ovarico resistente al platino. Un comunicato stampa allegato (Esibizione 99.1) fornisce ulteriori dettagli ed è incorporato per riferimento. Nessun risultato finanziario, previsione o informazione su transazioni è stata inclusa nella presentazione.

Questa presentazione della NDA rappresenta una tappa regolatoria importante che, se approvata, potrebbe diversificare le entrate di Corcept spostando l’azienda dal suo attuale focus sull’endocrinologia al mercato oncologico. I tempi di revisione da parte della FDA (tipicamente 10-12 mesi) e la successiva commercializzazione dipenderanno dall’accettazione e dall’approvazione dell’agenzia.

Corcept Therapeutics Incorporated (Nasdaq: CORT) presentó un Formulario 8-K con fecha 14 de julio de 2025 para revelar un evento corporativo material bajo el ítem 8.01 (Otros Eventos).

La compañía ha presentado una Solicitud de Nuevo Medicamento (NDA) a la Administración de Alimentos y Medicamentos de EE. UU. para su modulador selectivo de cortisol relacorilant destinado a tratar pacientes con cáncer de ovario resistente al platino. Un comunicado de prensa adjunto (Exhibición 99.1) proporciona detalles adicionales y se incorpora por referencia. No se acompañaron resultados financieros, pronósticos ni información transaccional con la presentación.

Esta presentación de la NDA representa un hito regulatorio significativo que, de ser aprobado, podría diversificar la base de ingresos de Corcept al expandir la compañía más allá de su enfoque actual en endocrinología hacia el mercado oncológico. El tiempo de revisión de la FDA (usualmente 10-12 meses) y la eventual comercialización dependen de la aceptación y aprobación de la agencia.

Corcept Therapeutics Incorporated (나스닥: CORT)는 2025년 7월 14일자 Form 8-K를 제출하여 항목 8.01(기타 사건) 하에 중요한 기업 이벤트를 공시했습니다.

회사는 백금 내성 난소암 환자 치료를 위한 선택적 코티솔 조절제 relacorilant에 대해 미국 식품의약국(FDA)에 신약 신청서(NDA)를 제출했습니다. 첨부된 보도자료(증거물 99.1)는 추가 세부 정보를 제공하며 참조용으로 포함되어 있습니다. 재무 결과, 가이드라인 또는 거래 정보는 제출서에 포함되지 않았습니다.

이번 NDA 제출은 중요한 규제 이정표로, 승인될 경우 Corcept가 현재 내분비학 중심에서 벗어나 종양학 시장으로 사업 영역을 확장하여 수익 기반을 다양화할 수 있습니다. FDA 검토 기간(통상 10-12개월)과 최종 상용화는 기관의 수락 및 승인 여부에 달려 있습니다.

Corcept Therapeutics Incorporated (Nasdaq : CORT) a déposé un formulaire 8-K daté du 14 juillet 2025 pour divulguer un événement d’entreprise important selon l’item 8.01 (Autres événements).

La société a soumis une demande d’autorisation de mise sur le marché (NDA) à la Food and Drug Administration des États-Unis pour son modulateur sélectif du cortisol relacorilant destiné au traitement des patientes atteintes d’un cancer de l’ovaire résistant au platine. Un communiqué de presse joint (Exhibit 99.1) fournit des détails supplémentaires et est incorporé par référence. Aucun résultat financier, prévision ou information transactionnelle n’a accompagné ce dépôt.

Cette soumission de la NDA représente une étape réglementaire importante qui, si elle est approuvée, pourrait diversifier les sources de revenus de Corcept en étendant l’activité de la société au-delà de son focus actuel en endocrinologie vers le marché de l’oncologie. Le délai d’examen de la FDA (généralement 10 à 12 mois) et la commercialisation éventuelle restent soumis à l’acceptation et à l’approbation de l’agence.

Corcept Therapeutics Incorporated (Nasdaq: CORT) reichte am 14. Juli 2025 ein Formular 8-K ein, um ein wesentliches Unternehmensereignis gemäß Punkt 8.01 (Sonstige Ereignisse) offenzulegen.

Das Unternehmen hat einen Antrag auf Zulassung eines neuen Medikaments (NDA) bei der US-amerikanischen Food and Drug Administration für seinen selektiven Cortisol-Modulator relacorilant eingereicht, um Patienten mit platinresistentem Eierstockkrebs zu behandeln. Eine beigefügte Pressemitteilung (Anlage 99.1) enthält weitere Details und ist durch Verweis Bestandteil der Einreichung. Finanzielle Ergebnisse, Prognosen oder Transaktionsinformationen wurden nicht beigefügt.

Diese NDA-Einreichung stellt einen bedeutenden regulatorischen Meilenstein dar, der, wenn genehmigt, Corcepts Umsatzbasis diversifizieren und das Unternehmen über seinen bisherigen Schwerpunkt auf Endokrinologie hinaus in den Onkologiemarkt führen könnte. Der Zeitrahmen für die FDA-Prüfung (in der Regel 10-12 Monate) und die anschließende Kommerzialisierung hängen von der Annahme und Zulassung durch die Behörde ab.

Positive
  • NDA submission for relacorilant achieves a major regulatory milestone, positioning CORT for potential entry into the ovarian cancer market.
  • Diversification opportunity beyond endocrinology could broaden revenue streams and reduce single-product dependence.
Negative
  • No assurance of FDA approval; clinical and regulatory risks remain until the agency’s decision.
  • No financial metrics or guidance were provided, leaving investors without visibility on potential launch costs or revenue impact.

Insights

TL;DR Corcept’s NDA for relacorilant targets unmet ovarian cancer need; milestone is strategically positive but approval and revenue remain uncertain.

The NDA submission is the final, pivotal step before potential U.S. market entry. Relacorilant addresses platinum-resistant ovarian cancer, a population with limited options, which strengthens the drug’s clinical and economic value proposition. Regulatory acceptance would validate Corcept’s cortisol modulation platform and create a second commercial franchise. Investors should watch for FDA filing acceptance (60-day clock) and potential Priority Review designation, which could shorten timelines. While the step is positive, approval risk and commercialization costs temper immediate valuation impact.

TL;DR NDA filing boosts pipeline visibility, but regulatory, reimbursement and competitive hurdles could delay monetization.

Although NDA submission signals sufficient clinical evidence, FDA may issue a Complete Response Letter if safety or efficacy questions persist. Competitive agents (e.g., PARP inhibitors) and payer scrutiny could limit uptake. Absence of disclosed financial projections suggests potential dilution if further funding is required for launch. Overall risk profile has improved, yet investors should model a 12-18-month approval window and probability-weighted revenues.

Corcept Therapeutics Incorporated (Nasdaq: CORT) ha presentato un modulo Form 8-K datato 14 luglio 2025 per comunicare un evento aziendale rilevante ai sensi della voce 8.01 (Altri Eventi).

L'azienda ha inviato una New Drug Application (NDA) alla Food and Drug Administration degli Stati Uniti per il suo modulatore selettivo del cortisolo relacorilant, destinato al trattamento di pazienti con carcinoma ovarico resistente al platino. Un comunicato stampa allegato (Esibizione 99.1) fornisce ulteriori dettagli ed è incorporato per riferimento. Nessun risultato finanziario, previsione o informazione su transazioni è stata inclusa nella presentazione.

Questa presentazione della NDA rappresenta una tappa regolatoria importante che, se approvata, potrebbe diversificare le entrate di Corcept spostando l’azienda dal suo attuale focus sull’endocrinologia al mercato oncologico. I tempi di revisione da parte della FDA (tipicamente 10-12 mesi) e la successiva commercializzazione dipenderanno dall’accettazione e dall’approvazione dell’agenzia.

Corcept Therapeutics Incorporated (Nasdaq: CORT) presentó un Formulario 8-K con fecha 14 de julio de 2025 para revelar un evento corporativo material bajo el ítem 8.01 (Otros Eventos).

La compañía ha presentado una Solicitud de Nuevo Medicamento (NDA) a la Administración de Alimentos y Medicamentos de EE. UU. para su modulador selectivo de cortisol relacorilant destinado a tratar pacientes con cáncer de ovario resistente al platino. Un comunicado de prensa adjunto (Exhibición 99.1) proporciona detalles adicionales y se incorpora por referencia. No se acompañaron resultados financieros, pronósticos ni información transaccional con la presentación.

Esta presentación de la NDA representa un hito regulatorio significativo que, de ser aprobado, podría diversificar la base de ingresos de Corcept al expandir la compañía más allá de su enfoque actual en endocrinología hacia el mercado oncológico. El tiempo de revisión de la FDA (usualmente 10-12 meses) y la eventual comercialización dependen de la aceptación y aprobación de la agencia.

Corcept Therapeutics Incorporated (나스닥: CORT)는 2025년 7월 14일자 Form 8-K를 제출하여 항목 8.01(기타 사건) 하에 중요한 기업 이벤트를 공시했습니다.

회사는 백금 내성 난소암 환자 치료를 위한 선택적 코티솔 조절제 relacorilant에 대해 미국 식품의약국(FDA)에 신약 신청서(NDA)를 제출했습니다. 첨부된 보도자료(증거물 99.1)는 추가 세부 정보를 제공하며 참조용으로 포함되어 있습니다. 재무 결과, 가이드라인 또는 거래 정보는 제출서에 포함되지 않았습니다.

이번 NDA 제출은 중요한 규제 이정표로, 승인될 경우 Corcept가 현재 내분비학 중심에서 벗어나 종양학 시장으로 사업 영역을 확장하여 수익 기반을 다양화할 수 있습니다. FDA 검토 기간(통상 10-12개월)과 최종 상용화는 기관의 수락 및 승인 여부에 달려 있습니다.

Corcept Therapeutics Incorporated (Nasdaq : CORT) a déposé un formulaire 8-K daté du 14 juillet 2025 pour divulguer un événement d’entreprise important selon l’item 8.01 (Autres événements).

La société a soumis une demande d’autorisation de mise sur le marché (NDA) à la Food and Drug Administration des États-Unis pour son modulateur sélectif du cortisol relacorilant destiné au traitement des patientes atteintes d’un cancer de l’ovaire résistant au platine. Un communiqué de presse joint (Exhibit 99.1) fournit des détails supplémentaires et est incorporé par référence. Aucun résultat financier, prévision ou information transactionnelle n’a accompagné ce dépôt.

Cette soumission de la NDA représente une étape réglementaire importante qui, si elle est approuvée, pourrait diversifier les sources de revenus de Corcept en étendant l’activité de la société au-delà de son focus actuel en endocrinologie vers le marché de l’oncologie. Le délai d’examen de la FDA (généralement 10 à 12 mois) et la commercialisation éventuelle restent soumis à l’acceptation et à l’approbation de l’agence.

Corcept Therapeutics Incorporated (Nasdaq: CORT) reichte am 14. Juli 2025 ein Formular 8-K ein, um ein wesentliches Unternehmensereignis gemäß Punkt 8.01 (Sonstige Ereignisse) offenzulegen.

Das Unternehmen hat einen Antrag auf Zulassung eines neuen Medikaments (NDA) bei der US-amerikanischen Food and Drug Administration für seinen selektiven Cortisol-Modulator relacorilant eingereicht, um Patienten mit platinresistentem Eierstockkrebs zu behandeln. Eine beigefügte Pressemitteilung (Anlage 99.1) enthält weitere Details und ist durch Verweis Bestandteil der Einreichung. Finanzielle Ergebnisse, Prognosen oder Transaktionsinformationen wurden nicht beigefügt.

Diese NDA-Einreichung stellt einen bedeutenden regulatorischen Meilenstein dar, der, wenn genehmigt, Corcepts Umsatzbasis diversifizieren und das Unternehmen über seinen bisherigen Schwerpunkt auf Endokrinologie hinaus in den Onkologiemarkt führen könnte. Der Zeitrahmen für die FDA-Prüfung (in der Regel 10-12 Monate) und die anschließende Kommerzialisierung hängen von der Annahme und Zulassung durch die Behörde ab.

7/8/20250000045012false00000450122025-07-082025-07-08

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

Date of Report (Date of earliest event reported): July 8, 2025

HALLIBURTON COMPANY
(Exact name of registrant as specified in its charter)
Delaware
001-0349275-2677995
(State or other jurisdiction of incorporation)(Commission File Number)(IRS Employer Identification No.)
3000 North Sam Houston Parkway East,Houston,Texas77032
(Address of principal executive offices)(Zip Code)
Registrant’s telephone number, including area code: (281) 871-2699
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:
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 classTrading SymbolName of each exchange on which registered
Common Stock, par value $2.50 per shareHALNew York Stock Exchange
NYSE Texas, Inc.

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
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 5.02. Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory Arrangements of Certain Officers.

On July 8, 2025, Charles E. Geer, Jr., Senior Vice President and Chief Accounting Officer of Halliburton Company (“Halliburton”), provided notice of his resignation from such positions, effective July 16, 2025 as to the Chief Accounting Officer position and July 31, 2025 as to the Senior Vice President position, in order to pursue another opportunity outside of the energy services industry. Mr. Geer’s resignation was not the result of any disagreement with Halliburton on any matter relating to the operations, policies or practices of Halliburton.

On July 9, 2025, Halliburton’s Board of Directors appointed Stephanie Holzhauser as Senior Vice President and Chief Accounting Officer of Halliburton, effective July 16, 2025. In connection with her appointment, Ms. Holzhauser will serve as the principal accounting officer of Halliburton.

Ms. Holzhauser, age 45, has served in roles of increasing responsibility in the Finance and Accounting departments at Halliburton, most recently as Vice President of Operations Finance at Halliburton since April 2023. Prior to that, she served as Vice President of Finance, Western Hemisphere at Halliburton from September 2021 to April 2023 and Senior Director of Finance Global Business Lines at Halliburton from 2016 to September 2021, as well as in numerous other roles with both Completion and Production and Drilling and Evaluation experience during her more than 20 years at Halliburton. Ms. Holzhauser holds a Bachelor’s degree in Accounting from Louisiana State University and a Master’s degree in Accounting from Louisiana State University.

There are no family relationships between Ms. Holzhauser and any director or executive officer of Halliburton. Phillip Spoelker, who is the brother of Ms. Holzhauser, is employed by Halliburton in a non-executive officer position and received total compensation of approximately $240,000 from January 1, 2024 through June 30, 2025. Mr. Spoelker’s compensation was established by Halliburton in accordance with its compensation practices applicable to employees with comparable qualifications and responsibilities and holding similar positions and is commensurate with that of his peers in Halliburton’s compensation framework. There are no arrangements or understandings between Ms. Holzhauser and any other persons pursuant to which she was selected as Senior Vice President and Chief Accounting Officer.

In connection with Ms. Holzhauser’s appointment, Halliburton entered into an Executive Agreement with Ms. Holzhauser effective July 16, 2025 (the “Employment Agreement”). The Employment Agreement provides for a minimum annual base salary of $450,000, participation in the Halliburton Annual Performance Pay Plan, the Halliburton Company Performance Unit Program, and the Halliburton Company Stock and Incentive Plan, and severance payments consistent with other executive officers of Halliburton, as well as other employee benefit plans and programs on the same basis generally as other executive officers of Halliburton. For additional information on these plans and programs, please read “Compensation Discussion and Analysis” in Halliburton’s Definitive Proxy Statement on Schedule 14A for Halliburton’s 2025 Annual Meeting of Shareholders filed with the Securities and Exchange Commission on April 1, 2025.

The foregoing description of the Employment Agreement does not purport to be complete and is qualified in its entirety by reference to the full text of the Employment Agreement, a copy of which is filed as Exhibit 10.1 to this Current Report on Form 8-K and is incorporated by reference herein.

In connection with Ms. Holzhauser’s appointment, Halliburton will also enter into an indemnification agreement with Ms. Holzhauser, effective July 16, 2025 and in the form generally provided to executive officers of Halliburton, a copy of which is included as Exhibit 10.33 to Halliburton’s Annual Report on Form 10-K for the fiscal year ended December 31, 2024.





Item 7.01. Regulation FD Disclosure.

On July 14, 2025, Halliburton issued a press release announcing a new Chief Accounting Officer, a copy of which is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated by reference herein.

The information furnished pursuant to this Item 7.01, including Exhibit 99.1, shall not be deemed to be “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall such information be deemed incorporated by reference into any registration statement or other filing under the Securities Act of 1933, as amended, or the Exchange Act, unless specifically identified in such filing as being incorporated by reference in such filing.

Item 9.01. Financial Statements and Exhibits.

(d) Exhibits.

10.1 Executive Agreement effective as of July 16, 2025, between Halliburton Energy Services, Inc. and Stephanie Holzhauser.

99.1 Press Release of Halliburton Company, dated July 14, 2025.

104 Cover Page Interactive Data File - the cover page XBRL tags are embedded within the Inline XBRL document.







SIGNATURES

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.



HALLIBURTON COMPANY
Date: July 14, 2025By:/s/ Pamela L. Taylor
Pamela L. Taylor
Vice President, Public Law and Assistant Secretary





FAQ

What material event did Corcept Therapeutics (CORT) report on July 14, 2025?

The company reported submitting an NDA to the FDA for relacorilant to treat platinum-resistant ovarian cancer.

Which drug is included in Corcept's new NDA?

Relacorilant, a selective cortisol modulator.

What indication is Corcept targeting with relacorilant?

Treatment of platinum-resistant ovarian cancer.

Does the 8-K include financial results or earnings data?

No, the filing only discloses the NDA submission; no financial metrics were provided.

Where can investors find more details about the NDA submission?

An attached press release is filed as Exhibit 99.1 to the Form 8-K.

What is the trading symbol for Corcept Therapeutics?

The company’s common stock trades on Nasdaq under the symbol CORT.
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