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10.1530/joe-22-0224 67 Romero-GmezM.LawitzE.ShankarR
In explaining its decision which is a victory for Novo and Lilly and will rework choices for consumers the FDA explained these compounders no longer meet the legal requirements to market their products
In clinical trials, higher-dose retatrutide produced average weight loss of around 2428% over longer treatment periods
The Company's view was also grounded in state-specific laws narrowly restricting how collateral such as inventory and licenses may be sold or transferred
Retatrutide remains in phase 3 clinical development under the TRIUMPH program and is not approved by the FDA, EMA, or MHRA for commercial or personal use
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