Unicycive Therapeutics presentation highlights OLC NDA review for dialysis hyperphosphatemia treatment

Reuters03-30

Unicycive <a href="https://laohu8.com/S/LENZ">Therapeutics</a> presentation highlights OLC NDA review for dialysis hyperphosphatemia treatment

Unicycive highlighted oxylanthanum carbonate (OLC) as lead program for hyperphosphatemia in chronic kidney disease patients on dialysis.
FDA accepted OLC NDA resubmission with PDUFA date set for June 29, 2026.
Resubmission followed Type A FDA meeting addressing a complete response letter deficiency tied to compliance status of a third-party manufacturing vendor.
Company projected cash runway into 2027 to support potential OLC approval and launch.
Pipeline update also included UNI-494 in development for acute kidney injury.

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 on March 30, 2026, and is solely responsible for the information contained therein.

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