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Conclusion Japanese patients with T2D appear to prefer oral GLP-1 RA profiles over injectable GLP-1 RA profiles, and administration appears to be the most important factor in this decision

Part of a structured dose-escalation program

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Novo Nordisk says the US FDA has approved a once daily pill

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On Tuesday, the 26th, the National Health Surveillance Agency (Anvisa) published the registration of the drug Ozivy, the first synthetic semaglutide pen analogous to the biological product released for commercialization in Brazil and uses the same active ingredient as Ozempic, whose patent expired on March 20th.