UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
CURRENT REPORT
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| Item 8.01 | Other Events. |
On November 27, 2023, Neumora Therapeutics, Inc. (“Neumora” or the “Company”) announced that NMRA-266 had received investigational new drug (IND) clearance from the U.S. Food and Drug Administration (FDA) and that it has initiated a Phase 1 single ascending dose / multiple ascending dose study evaluating NMRA-266 in healthy adult participants. NMRA-266 is an investigational positive allosteric modulator of the M4 muscarinic receptor subtype that Neumora exclusively licensed from The Warren Center for Neuroscience Drug Discovery at Vanderbilt University.
| Item 9.01 | Financial Statements and Exhibits. |
| Exhibit No. | Description | |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document) | |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| NEUMORA THERAPEUTICS, INC. | ||||||
| Date: November 28, 2023 | By: | /s/ Joshua Pinto | ||||
| Joshua Pinto | ||||||
| Chief Financial Officer | ||||||