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Dose-finding study of subcutaneously administered BI 456906 for 16 weeks, compared with placebo and open-label semaglutide in patients with type 2 diabetes mellitus

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In a cited study of 201 participants , after 2 weeks of treatment, 48.8% (98/201) reported improvement in anxiety symptoms, 36.3% (73/201) reported minimal change, and 14.9% (30/201) reported worsening, as described in Blossom Health's discussion of Lexapro response timing