SECURITIES AND EXCHANGE COMMISSION
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|Item 7.01.|| |
Regulation FD Disclosure.
On July 25, 2023, Tarsus Pharmaceuticals, Inc. (the “Company”) issued a press release announcing that the U.S. Food and Drug Administration (“FDA”) approved XDEMVY™ (lotilaner ophthalmic solution) 0.25% for the treatment of Demodex blepharitis.
Additionally, on July 25, 2023, the Company presented a webcast relating to the FDA approval of XDEMVY. The corporate presentation and a replay of the webcast of the event can be accessed on the “events” section of the Company’s Investor website at https://ir.tarsusrx.com/events-and-presentations/events#past-events.
The information in this Report is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (“Exchange Act”), or otherwise subject to the liabilities of that Section, and shall not be deemed incorporated by reference in any registration statement or other filing pursuant to the Securities Act of 1933, as amended, or the Exchange Act, except as otherwise expressly stated in such filing.
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.
|Tarsus Pharmaceuticals, Inc.|
|Date: July 25, 2023||By:|
|Jeffrey S. Farrow|
|Chief Financial Officer and Chief Strategy Officer|