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Koole et al., 2010
As in previous studies, we classified patents into those filed before FDA approval (pre-approval patents) and after (post-approval patents), and we classified regulatory exclusivities into those granted at FDA approval (approval exclusivities) and after (post-approval exclusivities)
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GLP-1s by year and indication GLP-1s by indication and year GLP-1 pipeline FAQs On March 19, 2026, the FDA approved a new, high-dose semaglutide (Wegovy HD) injection (7.2 mg) for once-weekly, subcutaneous (SC) administration for weight reduction and long-term maintenance
It can confirm that the patient is having a positive response to GLP-1 therapy after a certain time frame (e.g., six months)
Bckberg M, Hervieu G, Wilson S, Meister B
