Revelation Biosciences Inc. has announced positive top-line results from its Phase 1b PRIME clinical study involving its investigational product, Gemini, in patients with stage 3 and 4 chronic kidney disease (CKD). The study successfully met its primary endpoint, demonstrating the safety and tolerability of escalating doses of Gemini. Additionally, Gemini significantly reduced inflammatory activity and restored normal cellular responses, as indicated by measurements taken from peripheral blood mononuclear cells at various intervals post-dose. The results suggest Gemini's potential in rebalancing inflammation, which could benefit both acute and chronic inflammatory conditions. These findings were presented in a webcast/conference call held on September 10, 2025. Revelation Biosciences plans to publish these results and continue further data analysis.
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. Revelation Biosciences Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1070490) on September 09, 2025, and is solely responsible for the information contained therein.
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