Revelation Biosciences (REVB) announced that dosing has been completed for the PRIME Phase 1b clinical study of escalating doses of intravenously administered Gemini in patients with Stage 3 and 4 Chronic Kidney Disease. A total of five cohorts were enrolled at three clinics in the U.S. The company expects to share study data, including safety parameters and biomarkers of activity, during Q3 2025.
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