The medical misuse and non-medical use of prescription opioid analgesics is a significant problem in USA and its societal effects and cost have been well documented. The emergence of abuse deterrent opioid products into the marketplace is targeted to stem the advance of this complex problem. Although new abuse deterrent opioid products have been introduced which deter manipulation of the product for intravenous and intranasal routes of administration, none of the currently marketed abuse deterrent products address the most prevalent route of opioid misuse and abuse, excess oral consumption. The recent FDA guidance on abuse deterrent opioids clearly notes the lack of an abuse deterrent technology to deter excess oral consumption. Acura Pharmaceuticals Inc. (Acura) is a small specialty pharmaceutical company focused on the development and commercialization of abuse deterrent products to deter medication abuse and misuse. Acura's Aversion(R) technology is contained in Pfizer's Oxecta immediate release oxycodone tablets, where intranasal and intravenous mechanisms are employed. Acura is now actively involved in developing a technology that will deter the misuse and abuse of opioid tablets when excess intact tablets are ingested. A self-regulating dose concept for an immediate release, opioid tablet with features to limit the release of opioid when excess tablets are swallowed, will be developed. In this concept, an opioid matrix particle is formed and mixed with buffering and antacid ingredients to comprise a tablet. Buffer/antacid levels per opioid dose are selected to only partially neutralize gastric acid such that the stomach remains relatively acidic (pH <4) and the opioid matrix releases the opioid for absorption. However, when excess doses are ingested, buffer/antacid quantities are sufficient to neutralize gastric acid and elevate stomach pH (greater than or equal to pH 4). Under these conditions, the release of opioid would be slowed or limited as the high gastric pH environment is unfavorable for release from the opioid matrix. A demonstration self-regulating product using alprazolam, a benzodiazepine, has been developed. All ingredients used in this product are FDA approved at appropriate levels. In-vitro release of a single dose shows an immediate alprazolam release but when multiple doses are tested the in-vitro release is delayed such that the time to peak release is significantly lengthened compared to alprazolam tablets without self-regulation. This concept would be expected to show similar results in-vivo, where a reduced rate of rise from excess oral consumption would provide a significant safety factor from overdosing and to deter drug seeking behavior by lessening the potential """"""""high"""""""". Based on this concept, Acura plans to complete product and clinical development for a self-regulating hydromorphone HCl tablet and to file a 505(b)2 NDA for product approval.

Public Health Relevance

Acura Pharmaceuticals Inc., a company focused on the development and commercialization of abuse deterrent products, is currently developing a technology that will deter the misuse and abuse of prescription opioid tablets when a number of tablets are swallowed, a research area of high importance as noted by the FDA1. A concept product has been developed and shows an immediate drug release of a single dose as intended, but drug release from multiple doses of concept product results in a significant delay in release compared to the same number of doses without concept. With a delayed time to peak drug levels from swallowing excess doses, a prescription opioid product containing this technology would provide a significant safety factor from overdosing by misuse and would deter drug seeking behavior by lessening the potential high of an abuser.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
1R44DA037921-01
Application #
8756316
Study Section
Special Emphasis Panel (ZDA1)
Program Officer
Hampson, Aidan
Project Start
2014-09-01
Project End
2015-02-28
Budget Start
2014-09-01
Budget End
2015-02-28
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Acura Pharmaceuticals, Inc.
Department
Type
DUNS #
City
Palatine
State
IL
Country
United States
Zip Code
60067