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39 This strategy involves seeking FDA approval for only those uses of a drug that are no longer protected by patents, while carving out patented indications

To keep track of your progress with GLP-1 therapy, pay attention to several important metrics

The FDA issued over 80 warning letters to GLP-1 compounders in 2025-2026 for making false or misleading claims, including suggesting their products are equivalent to FDA-approved drugs

Although there is much less published information on treatment outcomes among HIV/HCV co-infected than in HCV mono-infected patients, the likelihood of achieving an SVR is lower in HIV/HCV co-infected persons108-110

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