Item 7.01 Regulation FD Disclosure

On December 7, 2022, Moleculin Biotech, Inc. (the "Company"), issued a press release announcing that the U.S. Food and Drug Administration ("FDA") has granted Fast Track designation of WP1122 for the treatment of Glioblastoma Multiforme ("GBM").

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



99.1   Press Release dated December 7, 2022

104 Cover page Interactive Data File (formatted as Inline XBRL document)

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