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[8-K] Ramaco Resources, Inc. 9.00% Senior Notes due 2026 Reports Material Event

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

BioCardia (BCDA) filed an 8-K to report a regulatory milestone for its lead program, CardiAMP, an autologous cell therapy for advanced heart failure. On 24 Jul 2025 the company submitted the therapy for clinical consultation with Japan’s Pharmaceuticals and Medical Devices Agency (PMDA). The consultation is the first formal step in Japan’s approval pathway and, if successful, could grant access to a large heart-failure market that accounts for ~1 M patients annually.

The filing contains no financial data and does not change previously issued guidance. Management furnished, rather than filed, the accompanying press release as Exhibit 99.1, limiting liability under Exchange Act §18. No other items were reported.

Key takeaways: 1) positions CardiAMP for potential ex-US expansion; 2) signals regulatory momentum following U.S. pivotal trial progress; 3) near-term catalysts will depend on PMDA feedback timing and any additional study requirements.

BioCardia (BCDA) ha presentato un modulo 8-K per comunicare un traguardo regolatorio relativo al suo programma principale, CardiAMP, una terapia cellulare autologa per l'insufficienza cardiaca avanzata. Il 24 luglio 2025, l'azienda ha sottoposto la terapia a consultazione clinica con l'Agenzia giapponese per i farmaci e i dispositivi medici (PMDA). Questa consultazione rappresenta il primo passo formale nel percorso di approvazione in Giappone e, se avrà esito positivo, potrebbe aprire l'accesso a un vasto mercato dell'insufficienza cardiaca che conta circa 1 milione di pazienti all'anno.

La comunicazione non contiene dati finanziari e non modifica le precedenti previsioni. La direzione ha fornito, anziché depositare, il comunicato stampa allegato come Exhibit 99.1, limitando così la responsabilità ai sensi della Sezione 18 del Exchange Act. Non sono stati segnalati altri elementi.

Punti chiave: 1) posiziona CardiAMP per un'espansione potenziale al di fuori degli Stati Uniti; 2) indica un'accelerazione regolatoria a seguito dei progressi del trial cardine negli USA; 3) i catalizzatori a breve termine dipenderanno dai tempi di risposta della PMDA e da eventuali requisiti aggiuntivi per studi.

BioCardia (BCDA) presentó un formulario 8-K para informar sobre un hito regulatorio de su programa principal, CardiAMP, una terapia celular autóloga para insuficiencia cardíaca avanzada. El 24 de julio de 2025, la compañía sometió la terapia a consulta clínica con la Agencia de Productos Farmacéuticos y Dispositivos Médicos de Japón (PMDA). Esta consulta es el primer paso formal en el proceso de aprobación en Japón y, si tiene éxito, podría abrir el acceso a un gran mercado de insuficiencia cardíaca que representa aproximadamente 1 millón de pacientes anuales.

La presentación no contiene datos financieros y no modifica las guías previamente emitidas. La dirección proporcionó, en lugar de presentar, el comunicado de prensa adjunto como Exhibit 99.1, limitando la responsabilidad según la Sección 18 de la Ley de Intercambio. No se reportaron otros elementos.

Puntos clave: 1) posiciona a CardiAMP para una posible expansión fuera de EE.UU.; 2) señala un impulso regulatorio tras el progreso del ensayo pivotal en EE.UU.; 3) los catalizadores a corto plazo dependerán del tiempo de respuesta de la PMDA y de cualquier requisito adicional de estudios.

BioCardia (BCDA)는 주요 프로그램인 CardiAMP에 대한 규제 이정표를 보고하기 위해 8-K를 제출했습니다. CardiAMP는 진행성 심부전을 위한 자가 세포 치료제입니다. 2025년 7월 24일 회사는 이 치료제를 일본 의약품의료기기종합기구(PMDA)와의 임상 상담에 제출했습니다. 이 상담은 일본 승인 절차의 첫 공식 단계이며, 성공할 경우 연간 약 100만 명의 환자를 대상으로 하는 큰 심부전 시장에 접근할 수 있게 됩니다.

제출서류에는 재무 데이터가 포함되어 있지 않으며, 이전에 발표된 가이던스에도 변화가 없습니다. 경영진은 첨부된 보도자료(Exhibit 99.1)를 제출하지 않고 제공하여, 증권거래법 §18에 따른 책임을 제한했습니다. 다른 항목은 보고되지 않았습니다.

주요 요점: 1) CardiAMP의 미국 외 확장 가능성을 위치시킴; 2) 미국 중추 임상시험 진전에 따른 규제 모멘텀 신호; 3) 단기 촉매는 PMDA 피드백 시기와 추가 연구 요구 사항에 따라 달라질 것.

BioCardia (BCDA) a déposé un rapport 8-K pour annoncer une étape réglementaire concernant son programme principal, CardiAMP, une thérapie cellulaire autologue pour l'insuffisance cardiaque avancée. Le 24 juillet 2025, la société a soumis la thérapie pour une consultation clinique auprès de l'Agence japonaise des produits pharmaceutiques et des dispositifs médicaux (PMDA). Cette consultation constitue la première étape formelle dans le processus d'approbation au Japon et, si elle est réussie, pourrait ouvrir l'accès à un large marché de l'insuffisance cardiaque représentant environ 1 million de patients par an.

Le dépôt ne contient pas de données financières et ne modifie pas les prévisions précédemment émises. La direction a fourni, plutôt que déposé, le communiqué de presse joint en tant qu'Exhibit 99.1, limitant ainsi la responsabilité conformément à la section 18 du Exchange Act. Aucun autre élément n'a été signalé.

Points clés : 1) positionne CardiAMP pour une expansion potentielle hors des États-Unis ; 2) témoigne d'un élan réglementaire suite aux progrès de l'essai pivot aux États-Unis ; 3) les catalyseurs à court terme dépendront du calendrier des retours de la PMDA et de toute exigence d'études supplémentaires.

BioCardia (BCDA) hat eine 8-K eingereicht, um einen regulatorischen Meilenstein für sein führendes Programm CardiAMP, eine autologe Zelltherapie für fortgeschrittene Herzinsuffizienz, zu melden. Am 24. Juli 2025 reichte das Unternehmen die Therapie zur klinischen Beratung bei der japanischen Arzneimittel- und Medizinprodukteagentur (PMDA) ein. Die Beratung ist der erste formale Schritt im Zulassungsprozess in Japan und könnte bei Erfolg den Zugang zu einem großen Herzinsuffizienzmarkt mit etwa 1 Million Patienten jährlich ermöglichen.

Die Einreichung enthält keine finanziellen Daten und ändert keine zuvor veröffentlichten Prognosen. Das Management stellte die beigefügte Pressemitteilung als Exhibit 99.1 bereit, ohne sie einzureichen, um die Haftung gemäß Exchange Act §18 zu begrenzen. Weitere Punkte wurden nicht gemeldet.

Wesentliche Erkenntnisse: 1) positioniert CardiAMP für eine potenzielle Expansion außerhalb der USA; 2) signalisiert regulatorische Dynamik nach Fortschritten in der US-Zulassungsstudie; 3) kurzfristige Katalysatoren hängen vom Zeitpunkt des PMDA-Feedbacks und möglichen zusätzlichen Studienanforderungen ab.

Positive
  • Regulatory progress: First formal engagement with Japan’s PMDA could accelerate CardiAMP entry into a large Asian market.
  • Strategic optionality: Diversifies approval pathways beyond the U.S., potentially enhancing partnership leverage and valuation.
Negative
  • No financial updates: Filing offers no clarity on funding needs to support additional Japanese studies.
  • Regulatory uncertainty: Outcome of PMDA consultation unknown; potential for added trials could delay commercialization.

Insights

TL;DR: PMDA consultation shows progress; modestly positive but clinical and regulatory risks remain.

The PMDA clinical consultation is analogous to a pre-IND meeting with the FDA. While not an approval, it validates BioCardia’s intent to pursue the expedited Japan HCT/P framework, which can shorten time-to-market if pivotal data are accepted. With limited cash (<$10 M at last 10-Q), external partnerships or capital raises may be needed to fund any Japan-specific studies. Overall impact skews positive because it adds strategic optionality without immediate cost escalation, but investors should watch for agency feedback and financing plans.

TL;DR: Event is directionally positive yet not valuation-changing today.

The filing signals regulatory traction, which could improve sentiment around BCDA’s pipeline. However, without efficacy data or concrete timelines, the announcement does little to alter cash-burn trajectories or near-term revenue outlook. I classify the disclosure as modestly impactful: it strengthens the bull narrative on geographic optionality but does not materially de-risk the program. Hold rating maintained until PMDA meeting minutes clarify next steps.

BioCardia (BCDA) ha presentato un modulo 8-K per comunicare un traguardo regolatorio relativo al suo programma principale, CardiAMP, una terapia cellulare autologa per l'insufficienza cardiaca avanzata. Il 24 luglio 2025, l'azienda ha sottoposto la terapia a consultazione clinica con l'Agenzia giapponese per i farmaci e i dispositivi medici (PMDA). Questa consultazione rappresenta il primo passo formale nel percorso di approvazione in Giappone e, se avrà esito positivo, potrebbe aprire l'accesso a un vasto mercato dell'insufficienza cardiaca che conta circa 1 milione di pazienti all'anno.

La comunicazione non contiene dati finanziari e non modifica le precedenti previsioni. La direzione ha fornito, anziché depositare, il comunicato stampa allegato come Exhibit 99.1, limitando così la responsabilità ai sensi della Sezione 18 del Exchange Act. Non sono stati segnalati altri elementi.

Punti chiave: 1) posiziona CardiAMP per un'espansione potenziale al di fuori degli Stati Uniti; 2) indica un'accelerazione regolatoria a seguito dei progressi del trial cardine negli USA; 3) i catalizzatori a breve termine dipenderanno dai tempi di risposta della PMDA e da eventuali requisiti aggiuntivi per studi.

BioCardia (BCDA) presentó un formulario 8-K para informar sobre un hito regulatorio de su programa principal, CardiAMP, una terapia celular autóloga para insuficiencia cardíaca avanzada. El 24 de julio de 2025, la compañía sometió la terapia a consulta clínica con la Agencia de Productos Farmacéuticos y Dispositivos Médicos de Japón (PMDA). Esta consulta es el primer paso formal en el proceso de aprobación en Japón y, si tiene éxito, podría abrir el acceso a un gran mercado de insuficiencia cardíaca que representa aproximadamente 1 millón de pacientes anuales.

La presentación no contiene datos financieros y no modifica las guías previamente emitidas. La dirección proporcionó, en lugar de presentar, el comunicado de prensa adjunto como Exhibit 99.1, limitando la responsabilidad según la Sección 18 de la Ley de Intercambio. No se reportaron otros elementos.

Puntos clave: 1) posiciona a CardiAMP para una posible expansión fuera de EE.UU.; 2) señala un impulso regulatorio tras el progreso del ensayo pivotal en EE.UU.; 3) los catalizadores a corto plazo dependerán del tiempo de respuesta de la PMDA y de cualquier requisito adicional de estudios.

BioCardia (BCDA)는 주요 프로그램인 CardiAMP에 대한 규제 이정표를 보고하기 위해 8-K를 제출했습니다. CardiAMP는 진행성 심부전을 위한 자가 세포 치료제입니다. 2025년 7월 24일 회사는 이 치료제를 일본 의약품의료기기종합기구(PMDA)와의 임상 상담에 제출했습니다. 이 상담은 일본 승인 절차의 첫 공식 단계이며, 성공할 경우 연간 약 100만 명의 환자를 대상으로 하는 큰 심부전 시장에 접근할 수 있게 됩니다.

제출서류에는 재무 데이터가 포함되어 있지 않으며, 이전에 발표된 가이던스에도 변화가 없습니다. 경영진은 첨부된 보도자료(Exhibit 99.1)를 제출하지 않고 제공하여, 증권거래법 §18에 따른 책임을 제한했습니다. 다른 항목은 보고되지 않았습니다.

주요 요점: 1) CardiAMP의 미국 외 확장 가능성을 위치시킴; 2) 미국 중추 임상시험 진전에 따른 규제 모멘텀 신호; 3) 단기 촉매는 PMDA 피드백 시기와 추가 연구 요구 사항에 따라 달라질 것.

BioCardia (BCDA) a déposé un rapport 8-K pour annoncer une étape réglementaire concernant son programme principal, CardiAMP, une thérapie cellulaire autologue pour l'insuffisance cardiaque avancée. Le 24 juillet 2025, la société a soumis la thérapie pour une consultation clinique auprès de l'Agence japonaise des produits pharmaceutiques et des dispositifs médicaux (PMDA). Cette consultation constitue la première étape formelle dans le processus d'approbation au Japon et, si elle est réussie, pourrait ouvrir l'accès à un large marché de l'insuffisance cardiaque représentant environ 1 million de patients par an.

Le dépôt ne contient pas de données financières et ne modifie pas les prévisions précédemment émises. La direction a fourni, plutôt que déposé, le communiqué de presse joint en tant qu'Exhibit 99.1, limitant ainsi la responsabilité conformément à la section 18 du Exchange Act. Aucun autre élément n'a été signalé.

Points clés : 1) positionne CardiAMP pour une expansion potentielle hors des États-Unis ; 2) témoigne d'un élan réglementaire suite aux progrès de l'essai pivot aux États-Unis ; 3) les catalyseurs à court terme dépendront du calendrier des retours de la PMDA et de toute exigence d'études supplémentaires.

BioCardia (BCDA) hat eine 8-K eingereicht, um einen regulatorischen Meilenstein für sein führendes Programm CardiAMP, eine autologe Zelltherapie für fortgeschrittene Herzinsuffizienz, zu melden. Am 24. Juli 2025 reichte das Unternehmen die Therapie zur klinischen Beratung bei der japanischen Arzneimittel- und Medizinprodukteagentur (PMDA) ein. Die Beratung ist der erste formale Schritt im Zulassungsprozess in Japan und könnte bei Erfolg den Zugang zu einem großen Herzinsuffizienzmarkt mit etwa 1 Million Patienten jährlich ermöglichen.

Die Einreichung enthält keine finanziellen Daten und ändert keine zuvor veröffentlichten Prognosen. Das Management stellte die beigefügte Pressemitteilung als Exhibit 99.1 bereit, ohne sie einzureichen, um die Haftung gemäß Exchange Act §18 zu begrenzen. Weitere Punkte wurden nicht gemeldet.

Wesentliche Erkenntnisse: 1) positioniert CardiAMP für eine potenzielle Expansion außerhalb der USA; 2) signalisiert regulatorische Dynamik nach Fortschritten in der US-Zulassungsstudie; 3) kurzfristige Katalysatoren hängen vom Zeitpunkt des PMDA-Feedbacks und möglichen zusätzlichen Studienanforderungen ab.

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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 23, 2025

 

Ramaco Resources, Inc.

(Exact name of Registrant as specified in its Charter)

 

Delaware 001-38003 38-4018838
(State or other jurisdiction of
incorporation)

(Commission File Number) (IRS Employer Identification No.)

 

250 West Main Street, Suite 1900

Lexington, Kentucky 40507

(Address of principal executive offices)

 

Registrant’s telephone number, including area code: (859) 244-7455

 

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 class Trading Symbol(s) Name of each exchange on which registered
Class A common stock, $0.01 par value METC Nasdaq Global Select Market
Class B common stock, $0.01 par value METCB Nasdaq Global Select Market
9.00% Senior Notes due 2026METCL Nasdaq Global Select Market
8.375% Senior Notes due 2029 METCZ Nasdaq Global Select Market

 

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 1.01. Entry into a Material Definitive Agreement

 

Underwriting Agreement

 

On or about July 23, 2025, Ramaco Resources, Inc. (the “Company”) commenced a public offering (the “Notes Offering”) of 8.250% Senior Notes due 2030 (the “Notes”). The public offering price of the Notes is $25.00 per Note, which is 100% of the principal amount. The Company will receive net proceeds after discounts and commissions, and a structuring fee that the Company has agreed to pay the lead book-running manager, but before expenses, of approximately $55,000,000. The Company intends to use the net proceeds from the Notes Offering to redeem all of the Company’s outstanding 9.00% Senior Notes due 2026 (the “2026 Notes”), and for general corporate purposes, including funding the acceleration of rare earth development, funding future investments, making capital expenditures and funding working capital. In connection with the Notes Offering, on July 23, 2025, the Company entered into an Underwriting Agreement with Lucid Capital Markets, LLC as representative of the several underwriters named therein (the “Underwriters”), providing for, among other things, the sale by the Company and the purchase by the Underwriters, acting severally and not jointly, of $57,000,000 aggregate principal amount of the Notes.

 

Pursuant to the Underwriting Agreement, the Company has also granted the Underwriters a 30-day option to purchase up to an additional $8,000,000 aggregate principal amount of Notes. The offer and sale of the Notes was registered pursuant to a registration statement on Form S-3 (File No. 333- 274324), which was declared effective by the United States Securities and Exchange Commission on September 29, 2023. The Notes Offering is expected to close on July 31, 2025, subject to customary closing conditions. The Underwriting Agreement contains customary representations and warranties, agreements and obligations, and termination provisions.

 

The foregoing description of the Underwriting Agreement does not purport to be complete and is qualified in its entirety by reference to the full text of the Underwriting Agreement, which is filed as Exhibit 1.1 hereto and is incorporated herein by reference.

 

Third Amendment Agreement

 

In order to facilitate the Notes Offering, on July 23, 2025, the Company entered into a Third Amendment Agreement (the “Third Amendment Agreement”) by and among (i) the Company, Ramaco Development, LLC, RAM Mining, LLC, Ramaco Coal Sales, LLC, Ramaco Resources, LLC, Ramaco Resources Land Holdings, LLC, Ramaco Coal, Inc., Maben Coal LLC, Carbon Resources Development, Inc., and Ramaco Coal, LLC (collectively, the “Borrowers”); (ii) KeyBank National Association, as administrative agent and lender; (iii) Cadence Bank, as lender; (iv) Associated Bank, National Association, as lender; (v) City National Bank, as lender; (vi) Star Financial Bank, as lender; and (vii) Trustmark National Bank, as lender.

 

The Third Amendment Agreement amends that certain Second Amended and Restated Credit and Security Agreement (as amended from time to time, the “Credit Agreement”) dated February 15, 2023, by and among the Company, the other Borrowers named therein, the lenders named therein, and KeyBank National Association as agent and lender; which was first amended pursuant to that certain First Amendment Agreement dated May 3, 2024, and later amended pursuant to that certain Second Amendment Agreement dated November 21, 2024, by and among the Borrowers named therein, the lenders named therein, and KeyBank National Association as agent and lender.

 

The Third Amendment Agreement, among other things, amends the Credit Agreement by permitting Ramaco to incur additional indebtedness in the form of the Notes to be issued in the Note Offering, in an aggregate principal amount not to exceed $100,000,000 (such amount, the “2030 Unsecured Note Basket”) after all of the Company’s 2026 Notes that were issued in July 2021 are redeemed in full, and reduces the amount of “Permitted Additional Unsecured Debt” (as defined in the Credit Agreement) from $75,000,000 to $15,000,000 plus the unused portion of the 2030 Unsecured Note Basket.

 

The foregoing description of the Third Amendment Agreement does not purport to be complete and is qualified in its entirety by reference to the full text of the Third Amendment Agreement, which is filed as Exhibit 10.1 hereto and is incorporated herein by reference.

 

 

 

Item 2.03. Creation of a Direct Financial Obligation or an Obligation under an Off-Balance Sheet Arrangement of a Registrant.

 

The information included in Item 1.01 of this Current Report related to the Third Amendment Agreement is incorporated by reference into this Item 2.03.

 

Item 8.01 Other Events

 

On July 23, 2025, the Company issued a press release announcing the proposed Notes Offering. Additionally, on July 24, 2025, the Company issued a press release announcing the pricing of the Notes Offering. Copies of these press releases are attached to this Current Report on Form 8-K as Exhibits 99.1 and 99.2, respectively.

 

Item 9.01 Financial Statements and Exhibits

 

(d) Exhibits

 

Exhibit
No.
  Description
1.1   Underwriting Agreement, dated July 23, 2025, between Ramaco Resources, Inc. and Lucid Capital Markets, LLC, as representative of the several underwriters named therein.
10.1   Third Amendment Agreement, dated July 23, 2025, by and among Ramaco Resources, Inc., Ramaco Development, LLC, RAM Mining, LLC, Ramaco Coal Sales, LLC, Ramaco Resources, LLC, Ramaco Resources Land Holdings, LLC, Ramaco Coal, Inc., Maben Coal LLC, Carbon Resources Development, Inc., Ramaco Coal, LLC, as borrowers, the lenders party thereto, and KeyBank National Association as agent and lender (amending the Second Amended and Restated Credit and Security Agreement, dated February 15, 2023, by and among Ramaco Resources, Inc., the other borrowers party thereto, the lenders party thereto, and KeyBank National Association, as agent, lender, swing line lender and the issuer).
99.1   Press Release issued by Ramaco Resources, Inc. dated July 23, 2025
99.2   Press Release issued by Ramaco Resources, Inc. dated July 24, 2025
23.1   Consent of Weir International, Inc.
104   Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)

 

 

 

 

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.

 

  Ramaco Resources, Inc.
   
  By: /s/ Randall W. Atkins
    Name: Randall W. Atkins
    Title: Chairman and Chief Executive Officer

 

Date: July 24, 2025

 

 

 

FAQ

What did BioCardia (BCDA) announce in this 8-K?

The company submitted its CardiAMP heart-failure therapy for clinical consultation with Japan’s PMDA, an initial step toward Japanese approval.

Does the filing include any financial results for BioCardia?

No. The 8-K only covers the regulatory milestone; it contains no revenue, EPS, or guidance data.

Why is PMDA consultation important for BioCardia investors?

Positive PMDA feedback could shorten the Japanese approval process, opening a significant market and potentially increasing CardiAMP’s commercial value.

Is the accompanying press release considered "filed" under the Exchange Act?

No. It is furnished under Item 8.01, which limits liability under Section 18 and prevents automatic incorporation into other filings.

What are the next catalysts after this PMDA submission?

Investors should look for PMDA meeting minutes, any required additional studies, and updates on financing to support Japanese regulatory activities.
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