Clene reported a FY 2025 net loss of USD 26.17 million, narrowing 34% from the prior year. FY 2025 research and development expense fell 30% to USD 14.01 million, driven mainly by lower spending on the HEALEY ALS Platform Trial and RESCUE-ALS following completion of their blinded portions and open-label extensions. FY 2025 general and administrative expense decreased 31% to USD 9.23 million, reflecting lower insurance, legal, and public and investor relations costs. Cash and cash equivalents were USD 5.19 million at year-end, down 57%, and the company said its December 31, 2025 resources plus proceeds from a January 2026 registered direct offering are expected to fund operations to the end of Q3 2026. Rob Etherington said the next milestone is an in-person Type C FDA meeting expected by end of Q1 2026, with Clene planning to file an accelerated-approval NDA for CNM-Au8 in ALS by the end of June 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. Clene Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603120800PRIMZONEFULLFEED9670577) on March 12, 2026, and is solely responsible for the information contained therein.
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