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While showing promising metabolic effect, evidence for the application of GLP-1 RAs in smoking cessation is limited

Participants are randomized 1:1 to receive D+Q or placebo administered for two consecutive days out of every fifteen days across three months with an extended nine-month follow-up after the intervention

FDA has renewed its Science Board, a committee of 15 external experts, to advise it for another two years until 26 June 2028

The FDA declared that the national shortage designations for semaglutide and tirzepatide injection products have been resolved