Azitra reported a FY 2025 net loss of USD 11.0 million, with R&D expenses of USD 4.8 million and G&A expenses of USD 6.2 million. Cash and cash equivalents were USD 2.1 million as of December 31, 2025. During FY 2025, Azitra initiated a Phase 1/2 trial of ATR-04 for EGFR inhibitor-associated rash and dosed the first patient in Q3 2025; topline data from the first cohort is expected around mid-2026. For its lead program ATR-12 (ATR12-351) in Netherton syndrome, the company reported promising safety data in June 2025 with 50% of patients enrolled, and said topline Phase 1b data are anticipated in H2 2026. Azitra also announced positive preclinical data for ATR-01 in ichthyosis vulgaris in Q3 2025 and said IND-enabling studies will continue in 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Azitra Inc. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001701478-26-000014), on February 27, 2026, and is solely responsible for the information contained therein.
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