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Tesamorelin gained FDA approval in 2010 specifically for reducing visceral adipose tissue in HIV-associated lipodystrophy, with clinical trials showing 1518% reductions in visceral fat after 26 weeks at 2mg daily dosing

Mackintosh JA

For systemic or injectable use, interaction data is nonexistent, and the risk assessment defaults to the broader concerns already discussed: unverified purity, uncontrolled dosing, and absent human trials

Cysteine availability is the primary bottleneck because it is maintained at much lower intracellular concentrations than glutamate or glycine

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(PubMed) Sahebkar A, Simental-Mendia LE, Stefanutti C, Pirro M