Britain’s Indivior Plc, which is also evaluating a long-acting injectable in a late-stage study, received the U.S. FDA’s fast-track status on Thursday (5/26) for the treatment.
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Topics: AddictionApprovalBuprenorphineFDAImplantMethadoneOpioidProbuphineTreatment
ACEP Now: Vol 43 – No 11 – November 2024
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