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Initial Data from Lightlake Therapeutics Joint Clinical Trial with NIDA Shows Nasal Delivery of Naloxone for Opioid Overdose as a Promising Treatment
Date:12/3/2013

LONDON, Dec. 3, 2013 /PRNewswire/ -- Lightlake Therapeutics Inc. ("Lightlake" or the "Company") (OTC BB: LLTP), a biopharmaceutical company developing addiction treatments based on its expertise in opioid antagonists, has announced that the initial findings of its clinical trial with the National Institute on Drug Abuse ("NIDA"), part of the National Institutes of Health, supports Lightlake's intranasal delivery of naloxone as a promising innovative treatment for opioid overdose.

Initial data from the study shows that Lightlake's naloxone nasal spray potentially can be delivered into the blood stream at least as quickly as the injection process currently used by hospitals, first responders, and others treating opioid overdoses.

Naloxone is a medicine currently available through injection that can rapidly reverse the overdose of prescription and illicit opioids. Lightlake, in partnership with NIDA, commenced a two-week clinical trial on September 23rd, 2013 designed to evaluate Lightlake's intranasal naloxone application.

"Opioid addiction has reached epidemic levels and is affecting families across the socio-economic spectrum and our goal of creating an easier to use, more accessible form of naloxone is closer to becoming a reality," said Dr. Roger Crystal, CEO of Lightlake.  "With the initial goal of submitting an NDA in 2014, we will meet with the FDA to discuss the results from this study. The data will also allow us to apply our novel method to a wide range of various addictions that are currently affecting millions of people on a daily basis."

"Given our collaboration with NIDA and current understanding of the regulatory pathway with respect to our prospective opioid overdose reversal product, we anticipate incurring relatively low costs to reach an NDA submission with the FDA," said Kevin Pollack, CFO of Lightlake. "Upon the prospective
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SOURCE Lightlake Therapeutics Inc.
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