Oral varespladib for the treatment of snakebite envenoming in India and the USA (BRAVO): a phase II randomised clinical trial.

Abstract

Introduction

Snakebite envenoming (SBE) results in over 500 000 deaths or disabling injuries annually. Varespladib methyl, an oral inhibitor of secretory phospholipase A2, is a nearly ubiquitous component of snake venoms. We conducted a phase II clinical trial to assess efficacy and safety of oral varespladib methyl in patients bitten by venomous snakes.

Methods

This double-blind, randomised, placebo-controlled trial enrolled patients in emergency departments in India and the USA. Patients with SBE were randomly assigned (1:1) to receive varespladib methyl or placebo two times per day for 1 week. All patients received standard of care, including antivenom. The primary outcome was change in the composite Snakebite Severity Score (SSS) measuring the severity of envenoming, from baseline to the average composite SSS at 6 and 9 hours.

Results

Among 95 patients randomised August 2021 through November 2022, the most common snakebites were from Russell's vipers (n=29), copperheads (n=18) and rattlesnakes (n=14). The SSS improved from baseline to the average at 6 and 9 hours by 1.1 (95% CI, 0.7 to 1.6) in the varespladib group versus 1.5 (95% CI, 1.0 to 2.0) in the placebo group (difference -0.4, 95% CI, -0.8 to 0.1, p=0.13). While key secondary outcomes were not statistically different by treatment group, benefit was seen in the prespecified subgroup initiating study drug within 5 hours of bite (n=37). For this early treatment group, clinically important differences were observed for illness severity over the first week, patient-reported function on days 3 and 7 and complete recovery. No death or treatment emergent serious adverse event occurred.

Conclusion

For emergency department treatment of snakebites, the addition of varespladib to antivenom did not find evidence of difference for the primary outcome based on the SSS. A potentially promising signal of benefit was observed in patients initiating treatment within 5 hours of snakebite.

Department

Description

Provenance

Subjects

Animals, Humans, Snake Bites, Acetates, Benzoates, Keto Acids, Indoles, Antivenins, Treatment Outcome, Administration, Oral, Double-Blind Method, Adolescent, Adult, Middle Aged, United States, India, Female, Male, Young Adult

Citation

Published Version (Please cite this version)

10.1136/bmjgh-2024-015985

Publication Info

Gerardo, Charles J, Rebecca W Carter, Surendra Kumar, Farshad M Shirazi, Suneetha D Kotehal, Peter D Akpunonu, Ashish Bhalla, Richard B Schwartz, et al. (2024). Oral varespladib for the treatment of snakebite envenoming in India and the USA (BRAVO): a phase II randomised clinical trial. BMJ global health, 9(10). p. e015985. 10.1136/bmjgh-2024-015985 Retrieved from https://hdl.handle.net/10161/33689.

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Scholars@Duke

Gerardo

Charles J. Gerardo

Professor of Emergency Medicine

Dr. Gerardo is Professor and Chair for the Department of Emergency Medicine.  He graduated with honors from Stanford University with a Bachelor’s of Science in Biology, and received his MD degree from University of California, Davis.  He went on to complete his residency training in Emergency Medicine at Loma Linda University Medical Center.  He completed his Masters of Health Sciences from the Duke University Clinical Research and Training Program.  In 2000, he joined Emergency Medicine faculty at Duke University and has served in numerous educational, research and administrative leadership roles. His current research focuses on US and global snake envenomation using a variety of methodologies from transitional science and clinical trials to machine learning and implementation science. He has over 90 peer reviewed publications and book chapters, and is published in JAMA, PLOS Medicine, Annals of Emergency Medicine, Academic Emergency Medicine and Clinical Toxicology. 

Francis

Samuel Jarrod Francis

Assistant Professor of Emergency Medicine

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