FDA Rejects Implant Option
The Carlat Addiction Treatment Report, Volume 1, Number 2, August 2013
https://www.thecarlatreport.com/newsletter-issue/catrv1n2/
Issue Links: Learning Objectives | Editorial Information
Topics: Addiction
The FDA rejected a new medication to treat opioid addiction that would have been implanted under the skin. The implant, Probuphine, is a long-acting version of buprenophine that is implanted under the skin of the upper arm in a procedure that can be done in a physician’s office in about 10–15 minutes.
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