- Unicycive posted a net loss of USD 27 million for fiscal 2025, narrowing 28%.
- Operating loss improved to USD 30 million as total operating expenses fell 8% to USD 30 million.
- Research and development costs dropped 54% to USD 9.1 million, while general and administrative expense climbed 69% to USD 20 million.
- FDA accepted the resubmitted oxylanthanum carbonate NDA as a Class II complete response, setting a PDUFA target action date of June 29, 2026.
- Unicycive expects current cash to fund operations for more than 12 months from the date of the report.
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. Unicycive Therapeutics 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: 0001213900-26-035903), on March 30, 2026, and is solely responsible for the information contained therein.
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