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Participants and group assignments. A total of 242 intent‐to‐treat participants were randomly assigned 1.75:1 to NB + CLI and UC groups. AE, adverse event; LTFU, lost to follow‐up; Other, protocol deviation or withdrawal of consent; N/A, not applicable; CLI, comprehensive lifestyle intervention; NB, sustained release combination of naltrexone and bupropion; Wk 16, evaluation to continue treatment at week 16 visit.
