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For reference, tesamorelin's FDA label dose alone is 2 mg/day (or 1.28 mg/day for the EGRIFTA WR formulation), and ipamorelin has been studied around 100-300 mcg per dose
From there, a licensed Ro provider will review your information, and may or may not suggest taking an optional metabolic lab test to check your cholesterol, A1C, thyroid and kidney enzyme levels in order to determine whether youre a good candidate for GLP-1 treatment
The drugmaker stated that Orforgliprons positive Phase 3 ATTAIN-1 trial results have put it on track to submit to global regulatory agencies by the end of 2025
PMID 7598783.
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