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The typical treatment plan for diagnosed deficiency involves a loading phase of several injections over two weeks, followed by maintenance doses every 12 weeks

In the UK, this is included as a special warning and precaution in the Summary of Product Characteristics (SmPC) rather than a formal contraindication

From a theoretical pharmacological standpoint, combining a peptide with putative lipolytic activity (AOD 9604) with a potent triple incretin receptor agonist (retatrutide) could potentially amplify metabolic effects but this is speculative and raises the possibility of compounding adverse effects with no safety data to guide dosing or monitoring