Press Releases August 5, 2026 08:02 PM

Tarsus to Report Second Quarter 2026 Financial Results on Thursday, August 6, 2026

Tarsus Pharmaceuticals Announces Q2 2026 Financial Results Release and Corporate Update Webcast

By Jordan Park
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TARS

Tarsus Pharmaceuticals, Inc. will report its second quarter 2026 financial results on August 6, 2026, and host a live webcast providing a corporate update exploring advances in their eye care and infectious disease prevention pipeline.

Tarsus to Report Second Quarter 2026 Financial Results on Thursday, August 6, 2026
TARS
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Key Points

  • Q2 2026 financial results to be announced on August 6, 2026, with an accessible live webcast and recordings.
  • Tarsus Pharmaceuticals focuses on innovative treatments primarily in eye care, including FDA-approved XDEMVY® for Demodex blepharitis.
  • Pipeline includes Phase 2 developments for ocular rosacea (TP-04), Lyme disease prevention (TP-05), and an ocular antiseptic (IRX-101).

IRVINE, Calif., Aug. 05, 2026 (GLOBE NEWSWIRE) -- Tarsus Pharmaceuticals, Inc. (NASDAQ: TARS), today announced that it will host a live webcast at 5:00 a.m. PT / 8:00 a.m. ET on Thursday, August 6, 2026 to report its second quarter 2026 financial results and provide a corporate update.

Participants may access the webcast here. A recorded version of the call will be available on the website shortly after the completion of the webcast and will be archived there for approximately 90 days.

About Tarsus Pharmaceuticals, Inc.
Tarsus Pharmaceuticals, Inc. applies proven science and new technology to revolutionize treatment for patients, starting with eye care. Tarsus is advancing its pipeline to address several diseases with high unmet need across a range of therapeutic categories, including eye care, dermatology, and infectious disease prevention. XDEMVY® (lotilaner ophthalmic solution) 0.25% is FDA approved in the United States for the treatment of Demodex blepharitis. Tarsus is also developing TP-04 for the potential treatment of ocular rosacea and TP-05 as an oral tablet for the potential prevention of Lyme disease, both of which are in Phase 2, and IRX-101 for potential use as an ocular antiseptic.

Media Contact:
Adrienne Kemp
Vice President, Corporate Communications
(949) 922-0801
[email protected]

Investor Contact:
David Nakasone
Head of Investor Relations
(949) 620-3223
[email protected]


Risks

  • Clinical development risks associated with products in Phase 2 trials, including efficacy and regulatory approvals.
  • Market adoption risks for newly launched products in competitive eye care and infectious disease markets.
  • Potential volatility around quarterly financial results impacting investor sentiment.

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