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10.1038/s41419-017-0215-0 4 ArmangueT.LeypoldtF.MlagaI.Raspall-ChaureM.MartiI.NichterC.et al

At best, about half of all patients become unresponsive to their current therapy and need to be switched up to another, more toxic drug

In vivo research protocols typically use lower doses, with careful attention to hypoglycemia risk

The FDA may eventually pull unsafe peptides after testing and approve others, prompting big pharma to mass-produce a version that they can patent and sell

Label each aliquot clearly with concentration, date, and a unique identifier

How well the treatment is working is checked by looking at blood counts and symptoms