NEW YORK, April 22, 2015 /PRNewswire/ -- Lightlake Therapeutics Inc. (“Lightlake”) (OTCQB: LLTP), a biopharmaceutical company developing addiction treatments based on its expertise in opioid antagonists, announced today that Adapt Pharma Limited (“Adapt”), Lightlake’s partner for treating opioid overdose with intranasal naloxone, successfully completed a clinical study of intranasal naloxone.
The pharmacokinetic study compared intranasal naloxone with an injectable formulation of naloxone. The study met its objectives and demonstrated the intranasal formulation of naloxone delivered the targeted naloxone dose as expected. Naloxone is a U.S. Food and Drug Administration (FDA) approved agent that reverses the effects of opioid overdose. Presently, all FDA approved formulations of naloxone are injectable products. Adapt is collaborating with the U.S. National Institute on Drug Abuse (NIDA) to develop a nasal naloxone formulation that would be suitable for use in the community setting by non-medically trained personnel.
“This important study builds on the first NIDA Lightlake collaborative pharmacokinetic study. It continues to demonstrate that nasal naloxone is a very promising treatment for the reversal of opioid overdose with great potential to be used in the community,” stated Arvind Agrawal, Executive Vice President, Medical Affairs, at Lightlake. He added, “We have found that many caregivers in the community setting worry about accessing and administering injectable naloxone. Pharmacokinetic studies provide a regulatory path to bridging between formulations. Thus nasal naloxone could provide non-medically trained personnel with a simple and easily accessible tool to prevent death due to opioid overdose.”
According to CDC WONDER, an information resource of the Centers for Disease Control and Prevention (CDC), opioid overdose led to the loss of over 26,000 lives in America in 2013, a four-fold increase since 1999. The majority of deaths arose in a community setting (mostly at home) and approximately 70% were caused by prescription opioids.
In December 2014, Lightlake announced a licensing deal with a subsidiary of Adapt Pharma Limited. In exchange for licensing its opioid overdose reversal treatment, Lightlake could receive potential development and sales milestone payments of more than $55 million, plus up to double-digit royalties.
About Lightlake Therapeutics Inc.
Lightlake Therapeutics Inc., a biopharmaceutical company, is using its expertise in opioid antagonists to build a platform of innovative intranasal naloxone solutions to common addictions and related disorders. Lightlake has entered into a licensing deal with a subsidiary of Adapt Pharma Limited with respect to a treatment to reverse opioid overdoses, which have reached epidemic proportions in the United States. Lightlake also has collaborated on clinical trials with the National Institute on Drug Abuse, part of the National Institutes of Health, with respect to this treatment. In addition, Lightlake has completed a Phase II clinical trial to treat Binge Eating Disorder. For more information please visit: http://www.lightlaketherapeutics.com.
Forward-Looking Statements
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Corporate Contact:
Lightlake Therapeutics Inc.
445 Park Avenue, 9th Floor
New York, NY 10022
Dr. Roger Crystal, CEO
(212) 829-5546
investor.relations@lightlaketherapeutics.com
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SOURCE Lightlake Therapeutics Inc.
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