UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM
CURRENT REPORT
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Item 8.01 | Other Events. |
On January 25, 2022 Mind Medicine (MindMed) Inc. (the “Company”), issued a press release announcing that the U.S. Food and Drug Administration has allowed the Company’s Phase 2b dose-optimization trial of lysergic acid diethylamid (LSD) for the treatment of generalized anxiety disorder to proceed. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated into this Item 8.01 by reference.
Item 9.01 | Financial Statements and Exhibits. |
Exhibit No. | Description | |
99.1 | Press Release, dated January 25, 2022 | |
104 | Cover Page Interactive Data File (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.
MIND MEDICINE (MINDMED) INC. | ||
Date: January 25, 2022 | By: | /s/ Cynthia Hu |
Name: | Cynthia Hu | |
Title: | Chief Legal Officer & Secretary |