The US Food and Drug Administration (FDA) Psychopharmacologic Drugs Advisory Committee has voted by 11 members to one to recommend approval of lofexidine for the mitigation of opioid withdrawal symptoms.
Lofexidine is a non-opioid treatment from US WorldMeds, a privately-held specialty pharma that will market the drug under the brand name Lucemyra if it is approved.
"The agonizing symptoms of opioid withdrawal are one of the most powerful factors driving opioid dependence and addictive behaviors"
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