ZyVersa Therapeutics Announces IRB Approval of Phase 2a Clinical Trial Protocol to Evaluate Cholesterol Efflux Mediator™ VAR 200 in Patients with Diabetic Kidney Disease

https://www.globenewswire.com/news-release/2024/03/18/2847718/0/en/ZyVersa-Therapeutics-Announces-IRB-Approval-of-Phase-2a-Clinical-Trial-Protocol-to-Evaluate-Cholesterol-Efflux-Mediator-VAR-200-in-Patients-with-Diabetic-Kidney-Disease.html

WESTON, Fla., March 18, 2024 (GLOBE NEWSWIRE) — ZyVersa Therapeutics, Inc. (Nasdaq:ZVSA, or “ZyVersa”), a clinical stage specialty biopharmaceutical company developing first-in-class drugs for the treatment of renal and inflammatory diseases with high unmet medical needs, announces Institutional Review Board (IRB) approval of the Phase 2a clinical trial protocol to evaluate the efficacy and safety of Cholesterol Efflux Mediator VAR 200 in patients with diabetic kidney disease. The clinical trial is on track to begin in the first half of 2024.

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