Over two billion pounds of cyanide are produced annually in the United States for use in a variety of industries, and thus accidental or intentional exposure of civilians to cyanide is a real concern. Current treatments of cyanide poisoning must be given intravenously, limiting their use in a setting of mass casualties. Under support of the CounterACT Program, we have been developing the vitamin B12 analog cobinamide as a cyanide antidote, and have found it to be an extremely potent cyanide countermeasure in several animal species. Because of its high potency, and, additionally, high degree of water solubility, sufficient amounts can be given by intramuscular injection to rescue animals from two times the LD100 of cyanide. Cobinamide is stable in solution, and we are in serious negotiations with a company to package cobinamide in an autoinjector. We expect to have all preclinical chemical and animal studies completed by December, 2011, and be ready to embark on Phase I Clinical Trials in January, 2012. We will have sufficient funds to complete the preclinical studies through a no-cost extension of the current CounterACT grant. As a cyanide antidote, cobinamide will need to be approved by the Food and Drug Administration (FDA) through the Animal Rule Pathway, which is used when efficacy studies cannot ethically be performed in humans. Rigorous animal studies conducted under Good Laboratory Practice (GLP) conditions substitute for Phase II and III clinical trials. Phase I studies must, therefore, be correspondingly larger, and include la dose escalation and Ib extended safety studies. We now propose to conduct Phase la and Ib studies of cobinamide, first in healthy adults, and then in three special populations that would likely be exposed to cyanide in a civilian disaster: children, the aged, and renal-impaired subjects. The latter subjects are included, because cobinamide is excreted by the kidneys. Prior to the studies in children, toxicology and pharmacokinetic studies in juvenile animals will be performed at SRI International, Menlo Park, CA. As part of the proposed work, we plan to conduct GLP efficacy studies in one animal species at Battelle Memorial Institute, Cincinnati, OH, and to submit a New Drug Application (NDA) to the FDA. To document cobinamide's efficacy and determine its relative potency in humans, we plan to study cobinamide's effects on blood cyanide and thiocyanate concentrations in cigarette smokers. At the completion of the proposed work, cobinamide would be available to treat a large number of civilians exposed to cyanide.

Public Health Relevance

Cyanide is a rapidly acting poison that requires immediate treatment. Current cyanide therapies do not lend themselves well to treating a large number of poisoned persons. We propose to conduct Phase I clinical trials of a new cyanide antidote that could be given rapidly by intramuscular injection to many cyanide-exposed victims.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project--Cooperative Agreements (U01)
Project #
4U01NS058030-10
Application #
9135525
Study Section
Special Emphasis Panel (ZRG1-MDCN-J (50)R)
Program Officer
Jett, David A
Project Start
2006-09-27
Project End
2017-08-31
Budget Start
2017-03-01
Budget End
2017-08-31
Support Year
10
Fiscal Year
2017
Total Cost
$314,990
Indirect Cost
$111,113
Name
University of California San Diego
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Anantharam, Poojya; Whitley, Elizabeth M; Mahama, Belinda et al. (2017) Cobinamide is effective for treatment of hydrogen sulfide-induced neurological sequelae in a mouse model. Ann N Y Acad Sci 1408:61-78
Kalyanaraman, Hema; Ramdani, Ghania; Joshua, Jisha et al. (2017) A Novel, Direct NO Donor Regulates Osteoblast and Osteoclast Functions and Increases Bone Mass in Ovariectomized Mice. J Bone Miner Res 32:46-59
Bebarta, Vikhyat S; Brittain, Matthew; Chan, Adriano et al. (2017) Sodium Nitrite and Sodium Thiosulfate Are Effective Against Acute Cyanide Poisoning When Administered by Intramuscular Injection. Ann Emerg Med 69:718-725.e4
Brenner, Matthew; Azer, Sarah M; Oh, Kyung-Jin et al. (2017) Oral Glycine and Sodium Thiosulfate for Lethal Cyanide Ingestion. J Clin Toxicol 7:
Tsai, Chen S; Mao, Rong W; Tsai, Shirley C et al. (2017) Faraday Waves-Based Integrated Ultrasonic Micro-Droplet Generator and Applications. Micromachines (Basel) 8:
Kambale, K J; Ali, E R; Sadiki, N H et al. (2017) Lower sulfurtransferase detoxification rates of cyanide in konzo-A tropical spastic paralysis linked to cassava cyanogenic poisoning. Neurotoxicology 59:256-262
Jiang, Jingjing; Chan, Adriano; Ali, Sameh et al. (2016) Hydrogen Sulfide--Mechanisms of Toxicity and Development of an Antidote. Sci Rep 6:20831
Greenawald, Lee A; Boss, Gerry R; Reeder, Aaron et al. (2016) Development of a Hydrogen Sulfide End-of-Service-Life Indicator for Respirator Cartridges Using Cobinamide. Sens Actuators B Chem 230:658-666
Lee, Jangwoen; Mahon, Sari B; Mukai, David et al. (2016) The Vitamin B12 Analog Cobinamide Is an Effective Antidote for Oral Cyanide Poisoning. J Med Toxicol 12:370-379
Kadjo, Akinde F; Dasgupta, Purnendu K; Boss, Gerry R (2015) Comment on ""Rapid visual detection of blood cyanide"" by C. Männel-Croisé and F. Zelder, Analytical Methods, 2012, 4, 2632. Anal Methods 7:5707-5711

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