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Active NON-SBIR/STTR RPGS NIH (US)

Platinum Based Countermeasures and Combinations with Protective Agents

$5.9M USD

Funder NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Recipient Organization Purdue University
Country United States
Start Date Aug 20, 2024
End Date Jul 31, 2026
Duration 710 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10953968
Grant Description

ABSTRACT This project's primary endpoint focus will be efficiently rescuing toxic cyanide exposure using three distinct animal models. None of the current countermeasure options meet the requirements for the risk scenarios and objectives in PAR 22-209. There are continual threats of chemical exposure to human populations. Health and safety

measures in the workplace cannot fully mitigate the chances of unexpected or malicious use of chemical toxicants. Safe and effective countermeasures to a cyanide chemical exposures that can deploy in a variety of challenging emergency settings represent a continual unmet medical need. In addition to survival, mitigating the

sequel morbidities of toxic chemical exposures means another challenge for next-generation countermeasures. For metabolic poisons that reach high levels of exposure like cyanide, approaches to reverse the insult's effects are warranted to mitigate more prolonged-term effects. A team of investigators with experience in discovering

and developing countermeasures and therapeutic agents and expertise in medicinal chemistry, pharmacology, toxicology, discovery pharmaceutics, in vivo phenotypic screens, and complimentary animal models will pursue milestones established from 3 specific aims. Aim 1: To improve and down-select next-generation platinum (II)-

based countermeasure agents hydrogen cyanide scavengers with properties that meet the criteria for developability. Aim 2: To evaluate combinations of the metabolite glyoxylate with platinum (II)-based scavenger agents. Aim 3: To evaluate the efficacy and safety in a porcine model for cyanide intoxication of lead candidate

platinum (II)-based agents alone and in combinations with the metabolite glyoxylate.

All Grantees

Purdue University

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