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When designing clinical trials to support new indications for use of FDA-approved GLP-1s, applicants should: Consider ways to leverage existing data (e.g., public data or previous FDA findings) to reduce the size, scope, timeline, and cost of development

Quality, purity, potency, and consistency may differ from FDA-approved products

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If the program fits your situation after speaking with a licensed healthcare professional, current details are below

Holst, Damien J

Conducted by Prime Therapeutics and Magellan Rx Management (MRx), the review sifted through pharmacy and medical claims data for 3,364 people with insurance plans that cover the GLP-1 drugs