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[8-K] Moleculin Biotech, Inc. Reports Material Event

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

Moleculin Biotech, Inc. reported two corporate actions in this Current Report. Stockholders approved and the company filed a Certificate Amendment to increase authorized common shares from 100,000,000 to 500,000,000, which became effective upon filing with the Delaware Secretary of State on August 21, 2025. The company also furnished a press release dated August 27, 2025 announcing completion of its Phase 1B/2 (MB-106) clinical trial evaluating Annamycin combined with Cytarabine (referred to as AnnAraC) for treatment of subjects with acute myeloid leukemia (AML). The Certificate Amendment and the press release are attached as exhibits.

Moleculin Biotech, Inc. ha riportato due azioni societarie in questo Current Report. Gli azionisti hanno approvato e la società ha depositato un Certificate Amendment per aumentare le azioni ordinarie autorizzate da 100.000.000 a 500.000.000, efficace al momento del deposito presso il Segretario di Stato del Delaware il 21 agosto 2025. La società ha inoltre pubblicato un comunicato stampa datato 27 agosto 2025 che annuncia il completamento dello studio clinico di Fase 1B/2 (MB-106) che valuta Annamycin in combinazione con Cytarabine (indicato come AnnAraC) per il trattamento di soggetti con leucemia mieloide acuta (LMA). L'emendamento al certificato e il comunicato stampa sono allegati come exhibit.

Moleculin Biotech, Inc. informó sobre dos acciones corporativas en este Current Report. Los accionistas aprobaron y la compañía presentó un Certificate Amendment para aumentar las acciones ordinarias autorizadas de 100.000.000 a 500.000.000, que entró en vigor al ser registrado en la Secretaría de Estado de Delaware el 21 de agosto de 2025. La compañía también difundió un comunicado de prensa con fecha 27 de agosto de 2025 anunciando la finalización de su ensayo clínico de Fase 1B/2 (MB-106) que evalúa Annamycin combinado con Cytarabine (denominado AnnAraC) para el tratamiento de sujetos con leucemia mieloide aguda (LMA). El Certificate Amendment y el comunicado de prensa se adjuntan como exhibits.

Moleculin Biotech, Inc.는 본 Current Report에서 두 가지 회사 관련 조치를 보고했습니다. 주주들은 승인했으며 회사는 Certificate Amendment을 제출하여 승인된 보통주 수를 100,000,000에서 500,000,000으로 증액했으며, 이는 2025년 8월 21일 델라웨어 국무장관실에 제출되면서 효력이 발생했습니다. 회사는 또한 2025년 8월 27일자 보도자료를 제공하여 Annamycin과 Cytarabine 병용(명칭: AnnAraC)을 평가한 제1B/2상(MB-106) 임상시험이 완료되었음을 발표했습니다. Certificate Amendment와 보도자료는 전시자료로 첨부되어 있습니다.

Moleculin Biotech, Inc. a signalé deux décisions d'entreprise dans ce Current Report. Les actionnaires ont approuvé et la société a déposé un Certificate Amendment visant à augmenter les actions ordinaires autorisées de 100 000 000 à 500 000 000, qui est entré en vigueur lors du dépôt auprès du Secrétaire d'État du Delaware le 21 août 2025. La société a également publié un communiqué de presse daté du 27 août 2025 annonçant l'achèvement de son essai clinique de phase 1B/2 (MB-106) évaluant l'Annamycin en combinaison avec la Cytarabine (désigné AnnAraC) pour le traitement de sujets atteints de leucémie myéloïde aiguë (LMA). L'amendement au certificat et le communiqué de presse sont joints en tant qu'exhibits.

Moleculin Biotech, Inc. meldete in diesem Current Report zwei unternehmensbezogene Maßnahmen. Die Aktionäre stimmten zu und das Unternehmen reichte eine Certificate Amendment ein, um die genehmigten Stammaktien von 100.000.000 auf 500.000.000 zu erhöhen; diese Änderung wurde mit der Einreichung beim Secretary of State von Delaware am 21. August 2025 wirksam. Das Unternehmen veröffentlichte außerdem eine Pressemitteilung vom 27. August 2025, in der der Abschluss der Phase-1B/2-Studie (MB-106) bekanntgegeben wurde, in der Annamycin in Kombination mit Cytarabine (bezeichnet als AnnAraC) zur Behandlung von Patienten mit akuter myeloischer Leukämie (AML) bewertet wurde. Die Certificate Amendment und die Pressemitteilung sind als Exhibits beigefügt.

Positive
  • Certificate Amendment effective: authorized common shares increased from 100,000,000 to 500,000,000 and filed with Delaware on August 21, 2025
  • Clinical trial milestone: press release announced completion of the Phase 1B/2 (MB-106) trial evaluating Annamycin plus Cytarabine (AnnAraC) for AML on August 27, 2025
  • Exhibits furnished: Certificate Amendment filed as Exhibit 3.1 and press release furnished as Exhibit 99.1
Negative
  • None.

Insights

TL;DR: Company expanded authorized common shares and announced completion of a Phase 1B/2 trial for AnnAraC in AML.

The increase in authorized common shares to 500 million is a structural corporate change that provides the board flexibility for future equity actions; the filing confirms shareholder approval and effectiveness as of August 21, 2025. Separately, the furnished press release reports completion of the Phase 1B/2 MB-106 trial of Annamycin plus Cytarabine. Both developments are material company disclosures: one governance/capital-structure action and one clinical-stage program milestone. Investors will rely on the attached exhibits for full details.

TL;DR: Shareholders approved and the company filed an amendment increasing authorized common shares; the change is now effective.

The exhibit filing of the Certificate Amendment documents the formal amendment to the Amended and Restated Certificate of Incorporation, increasing authorized common stock from 100,000,000 to 500,000,000. The 8-K appropriately references the executed amendment as Exhibit 3.1 and includes the press release as Exhibit 99.1. This disclosure aligns with required reporting for charter amendments and Regulation FD furnishing for the press release.

Moleculin Biotech, Inc. ha riportato due azioni societarie in questo Current Report. Gli azionisti hanno approvato e la società ha depositato un Certificate Amendment per aumentare le azioni ordinarie autorizzate da 100.000.000 a 500.000.000, efficace al momento del deposito presso il Segretario di Stato del Delaware il 21 agosto 2025. La società ha inoltre pubblicato un comunicato stampa datato 27 agosto 2025 che annuncia il completamento dello studio clinico di Fase 1B/2 (MB-106) che valuta Annamycin in combinazione con Cytarabine (indicato come AnnAraC) per il trattamento di soggetti con leucemia mieloide acuta (LMA). L'emendamento al certificato e il comunicato stampa sono allegati come exhibit.

Moleculin Biotech, Inc. informó sobre dos acciones corporativas en este Current Report. Los accionistas aprobaron y la compañía presentó un Certificate Amendment para aumentar las acciones ordinarias autorizadas de 100.000.000 a 500.000.000, que entró en vigor al ser registrado en la Secretaría de Estado de Delaware el 21 de agosto de 2025. La compañía también difundió un comunicado de prensa con fecha 27 de agosto de 2025 anunciando la finalización de su ensayo clínico de Fase 1B/2 (MB-106) que evalúa Annamycin combinado con Cytarabine (denominado AnnAraC) para el tratamiento de sujetos con leucemia mieloide aguda (LMA). El Certificate Amendment y el comunicado de prensa se adjuntan como exhibits.

Moleculin Biotech, Inc.는 본 Current Report에서 두 가지 회사 관련 조치를 보고했습니다. 주주들은 승인했으며 회사는 Certificate Amendment을 제출하여 승인된 보통주 수를 100,000,000에서 500,000,000으로 증액했으며, 이는 2025년 8월 21일 델라웨어 국무장관실에 제출되면서 효력이 발생했습니다. 회사는 또한 2025년 8월 27일자 보도자료를 제공하여 Annamycin과 Cytarabine 병용(명칭: AnnAraC)을 평가한 제1B/2상(MB-106) 임상시험이 완료되었음을 발표했습니다. Certificate Amendment와 보도자료는 전시자료로 첨부되어 있습니다.

Moleculin Biotech, Inc. a signalé deux décisions d'entreprise dans ce Current Report. Les actionnaires ont approuvé et la société a déposé un Certificate Amendment visant à augmenter les actions ordinaires autorisées de 100 000 000 à 500 000 000, qui est entré en vigueur lors du dépôt auprès du Secrétaire d'État du Delaware le 21 août 2025. La société a également publié un communiqué de presse daté du 27 août 2025 annonçant l'achèvement de son essai clinique de phase 1B/2 (MB-106) évaluant l'Annamycin en combinaison avec la Cytarabine (désigné AnnAraC) pour le traitement de sujets atteints de leucémie myéloïde aiguë (LMA). L'amendement au certificat et le communiqué de presse sont joints en tant qu'exhibits.

Moleculin Biotech, Inc. meldete in diesem Current Report zwei unternehmensbezogene Maßnahmen. Die Aktionäre stimmten zu und das Unternehmen reichte eine Certificate Amendment ein, um die genehmigten Stammaktien von 100.000.000 auf 500.000.000 zu erhöhen; diese Änderung wurde mit der Einreichung beim Secretary of State von Delaware am 21. August 2025 wirksam. Das Unternehmen veröffentlichte außerdem eine Pressemitteilung vom 27. August 2025, in der der Abschluss der Phase-1B/2-Studie (MB-106) bekanntgegeben wurde, in der Annamycin in Kombination mit Cytarabine (bezeichnet als AnnAraC) zur Behandlung von Patienten mit akuter myeloischer Leukämie (AML) bewertet wurde. Die Certificate Amendment und die Pressemitteilung sind als Exhibits beigefügt.

false 0001659617 0001659617 2025-08-21 2025-08-21
 
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): August 21, 2025
 
a01.jpg
 
 
MOLECULIN BIOTECH, INC.
(Exact Name of Registrant as Specified in its Charter)
 
Delaware
001-37758
47-4671997
(State or Other Jurisdiction of
Incorporation or Organization)
(Commission File No.)
(I.R.S. Employer Identification
No.)
 
5300 Memorial Drive, Suite 950, Houston, TX 77007
(Address of principal executive offices and zip code)
 
(713) 300-5160
(Registrant’s telephone number, including area code)
 
(Former name or former address, if changed from 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-14(c))
 
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. ☐
 
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, par value $.001 per share
MBRX
The NASDAQ Stock Market LLC
 
 

 
 
Item 5.03
Amendments to Articles of Incorporation or Bylaws; Chang in Fiscal Year
 
As previously disclosed, at the Moleculin Biotech, Inc. (the “Company”) annual meeting of stockholders held on August 18, 2025, the Company’s stockholders approved, among other matters, a proposal to approve a Certificate of Amendment to the Company’s Amended and Restated Certificate of Incorporation (the “Certificate Amendment”) which would amend the Company’s existing certificate of incorporation, as amended, to increase the number of authorized shares of the Company’s common stock from 100,000,000 shares to 500,000,000 shares. The Certificate Amendment became effective upon filing with the Delaware Secretary of State on August 21, 2025.
 
A copy of the Certificate Amendment is filed as Exhibit 3.1 hereto and is incorporated in this Item 5.03 by reference.
 
Item 7.01
Regulation FD Disclosure
 
On August 27, 2025, Moleculin Biotech, Inc. (the “Company”), issued a press release which announced the completion of its Phase 1B/2 (MB-106) clinical trial evaluating Annamycin in combination with Cytarabine (also known as “Ara-C” and for which the combination of Annamycin and Ara-C is referred to as AnnAraC) for the treatment of subjects with acute myeloid leukemia (AML).
 
A copy of the press release is attached to this report as Exhibit 99.1 and is incorporated by reference herein.
 
The information contained in Item 7.01 of this Current Report on Form 8-K, including Exhibit 99.1, is being furnished and shall not be “filed” for the purpose of the Securities Exchange Act of 1934, as amended (“Exchange Act”), nor shall it be incorporated by reference in any filing under the Exchange Act or the Securities Act of 1933, as amended (“Securities Act”), unless specifically identified therein as being incorporated by reference.
 
Item 9.01
Financial Statements and Exhibits.
 
(d)
Exhibits.
 
Exhibit
No.
Description
 
3.1
Amendment to Amended and Restated Certificate of Incorporation of Moleculin Biotech, Inc., dated August 21, 2025
 
99.1
Press Release dated August 27, 2025
 
104
Cover page Interactive Data File (formatted as Inline XBRL document)
 
 
 
SIGNATURE
 
Pursuant to the requirements of the Securities and Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
 
 
MOLECULIN BIOTECH, INC. 
 
       
       
 
Date:
August 27, 2025
 
       
 
By:
/s/ Jonathan P. Foster
 
   
Jonathan P. Foster
 
 
 

FAQ

What change to authorized shares did Moleculin (MBRX) report?

The company increased authorized common stock from 100,000,000 to 500,000,000, effective upon filing on August 21, 2025.

Has Moleculin filed the Certificate Amendment?

Yes. The Certificate Amendment was filed with the Delaware Secretary of State and is attached as Exhibit 3.1 to the Current Report.

What clinical update did Moleculin (MBRX) disclose?

The company furnished a press release announcing completion of the Phase 1B/2 (MB-106) clinical trial evaluating Annamycin plus Cytarabine (AnnAraC) for AML on August 27, 2025.

Are the press release and amendment considered filed or furnished?

The Certificate Amendment is filed as an exhibit; the press release is furnished as Exhibit 99.1 and is expressly stated to be furnished, not filed, under the Exchange Act.
Moleculin Biotec

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