FDA Issues Guidance on Generic Abuse-Deterrent Opioid Development

NOVEMBER 21, 2017
Jennifer Barrett, Assistant Editor
Officials with the FDA have released a guidance on the development of generic abuse-deterrent opioids. The final guidance is part of the agency’s effort to reduce abuse by decreasing unnecessary exposure to opioids.

In an FDA statement, Scott Gottlieb, MD, FDA Commissioner, noted that increasing generic access is key to transitioning from the current market dominated by conventional opioids to abuse-deterrent formulations.

“We must have the potential to improve access to the newer formulations, for appropriately selected and monitored patients, through the introduction of generic competitors,” Dr. Gottlieb said in the statement.

The released guidance is intended to assist the industry in their development of generic versions of approved opioids with abuse-deterrent formulations (ADFs). The guidance aims to assist developers by clarifying the agency’s expectations prior to application submission to reduce time to approval. As part of the guidance, the FDA provides new recommendations about the type of studies companies should conduct to demonstrate that the generic drug is no less abuse-deterrent than its brand-name counterpart.

According to the statement, FDA officials have already approved 10 opioids with ADFs to date. Dr. Gottlieb noted that improved access to generic versions of these products could increase uptake by reducing barriers of cost.

In addition, the FDA is taking steps to expedite the process of getting ADFs to market by developing improved testing methodologies for evaluating complex features such as abuse deterrence for both brand name and generic opioid drug products. Other efforts include the development of new tools for speeding up generic development of complex products

According to Dr. Gottlieb, the intention of the new guidance is to decrease addiction rates and prevent unnecessary use of opioids. “This is an effort designed to encourage the shift – only when opioids are clinically appropriate – from existing, easily abused products to those that are harder to manipulate.”

For more on ADFs, see the video below. 



Reference

Statement from FDA Commissioner Scott Gottlieb, M.D., on steps to promote development of generic versions of opioids formulated to deter abuse [news release]. FDA’s website. https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm586117.htm. Accessed November 21, 2017.
 

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