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Both can prescribe GLP-1 receptor agonists such as semaglutide, and dual GIP/GLP-1 agonists such as tirzepatide, subject to clinical eligibility

Under the PDUFA, the FDA collects three types of user fees from new drug and biological product applications in order to facilitate faster approval: Application Fee Clinical Data Required Application Fee No Clinical Data Required Program Fee Fast Track Programs include the following: 1

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292 , F14711478, (2007)

Ambos son productos inyectables que deben administrarse una vez a la semana, pero su uso contra la obesidad no est todava indicado