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The FDA still has to decide what happens next
It is administered as a once-weekly subcutaneous injection in clinical trials, a delivery method consistent with other agents in the incretin-based therapy class, such as semaglutide and tirzepatide
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[99] In contrast to generics, which may be chemically synthesized versions manufactured using different processes than the original biologic drug, Health Canada confirmed that Plosbrio and Poviztra differ from the existing proprietary drugs Ozempic and Wegovy only in name and packaging, and are unrelated to the generics from a regulatory perspective
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