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34 The FOCUS Trial should shed light on how many patients treated with GLP-1/GIP agonists experience significant worsening of their DR and macular edema

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The businesses then pointed to the size of the market as evidence that regulators needed to accommodate it. Whats especially problematic, according to Ginsberg, is that now that compounding may move ahead, few lay consumers will understand the legal difference between an FDA-approved drug and a substance permitted for compounding

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2024 Nov;41(11):881-896