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Its strong stability in plasma, ease of solubility, and broad systemic activity make it a frequent subject in regenerative research

The committees recommendation is not a binding decision, and the addition of the peptides to the list will still have to go through a lengthy public rulemaking process

(1992) described the IGF-1 LR3 analog and documented its dramatically reduced IGFBP binding compared to native IGF-1, establishing the pharmacokinetic rationale for its use as a research tool (PMID 1601853)