Overview

Evaluation of the Safety and Tolerability of Gemini in Subjects With Stage 3-4 Chronic Kidney Disease.

Status:
RECRUITING
Trial end date:
2025-06-30
Target enrollment:
Participant gender:
Summary
Gemini is being evaluated in a placebo controlled, single dose, escalating dose study to evaluate the safety and tolerability of intravenous Gemini in adult subjects with stage 3 or 4 chronic kidney disease. Pharmacokinetics will be evaluated and measurements of the effect of Gemini on pharmacodynamic activity will be measured to assess changes in potential pharmacodynamic markers.
Phase:
PHASE1
Details
Lead Sponsor:
Revelation Biosciences, Inc