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While patients are showing some willingness to absorb cost hikes associated with reduced payer coverage for GLP-1 drugs, theyre far from the only stakeholders to be impacted by shifting policies: Biopharma Pharmaceutical developers could face slower market growth, particularly for newer indications like cardiovascular risk reduction and addiction treatment

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The FDA initially approved subcutaneous (SC) use Exenatide in 2005 and an oral version of semaglutide in 2019.2,3 Initially, GLP-1s were used exclusively for individuals with type 2 diabetes (T2DM) as a means to better control their blood sugar when paired with diet and exercise.2 Now their use is growing exponentially due to their success in helping patients achieve significant weight loss

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