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This means they do not require a marketing authorisation from the Medicines and Healthcare products Regulatory Agency (MHRA) before being sold, and manufacturers are not required to prove efficacy or conduct clinical trials prior to placing their products on the market
Data were pooled using random-effects models, and subgroup analyses were performed by drug type and treatment duration
Teva announces FDA approval and launch of generic Saxenda (liraglutide injection) first generic GLP-1 indicated for weight loss
doi: 10.3389/fmicb.2023.1125616 Received 16 December 2022 Accepted 13 March 2023 Published 11 April 2023 Volume 14 - 2023 Edited by Stavros Plessas, Democritus University of Thrace, Greece Reviewed by Alejandra Romo-Araiza, Anahuac University of North Mexico, Mexico
