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The FDA is in the midst of deciding whether to allow the seven peptides that were considered by the advisory committee to be compounded by licensed pharmacies
Do note that the FDA has not approved or allowed the production of generic variants in the United States yet, as the patent still holds in the US until early 2030
The SURPASS and SURMOUNT trialswhich led to FDA approval of tirzepatidedocumented systolic blood pressure reductions of 46 mmHg on average, with some patients seeing 10+ mmHg drops
Compounded GLP-1 medications have not undergone the same clinical trial review process as FDA-approved medications
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