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Bioavailability varies enormously depending on the peptide, the formulation, and the technique, ranging from 15 percent for some compounds to over 70 percent for others

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10.1101/cshperspect.a018812 Cold Spring Harb

Much less potency change for amylin receptor 3 activation was observed in contrast to the significant 5- to 10-fold potency enhancement shown for amylin receptor 1/2 and calcitonin receptor activation (Figure 9C and Table 3)

After 4 hours, the rate of clearance declined and plasma levels became more stable, exhibiting a relatively linear rate of decline suggesting a phase of pure elimination from 4 to 120 hours