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Nutrition 57 , 97108 (2019)
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Should Phase 3 trials demonstrate a favourable benefit-risk profile, Eli Lilly would be expected to submit a Marketing Authorisation Application (MAA) to the MHRA (and separately to the EMA for European markets) for regulatory review
"Following the interim analysis, I would say we're confident in MariTide's differentiated profile, and believe it will address important unmet medical needs," Bradway said
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He explains that if every American qualified to be on GLP-1saround 100 million peopleopted for them, this could double the current spending on all prescription drugs combined
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