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Nanexa AB announces today that the first patient has been dosed in the 30 mg dose group in the ongoing Phase I study with NEX-22, the company’s one-month formulation of liraglutide.

Nanexa AB announces that the phase I study with NEX-22, the company’s one-month formulation of liraglutide, will resume with further dose escalation with an expected start in the first quarter of 2025. The study will now continue to include patients after receiving regulatory approval to add a dose group for the administration of 30 mg liraglutide.