Dipeptidyl Peptidase-4 Inhibitor Pharmacokinetics

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 39: Line 39:
|-
|-
! [[Pharmacokinetics#Inhibitory_Concentration_.28IC50.29|IC<sub>50</sub>]] (nM)
! [[Pharmacokinetics#Inhibitory_Concentration_.28IC50.29|IC<sub>50</sub>]] (nM)
-
! [[Vildagliptin]]<br/>(Galvus)
+
! 3
-
! [[Sitagliptin]]<br/>(Januvia)
+
! 18
! [[Saxagliptin]]<br/>(Onglyza)
! [[Saxagliptin]]<br/>(Onglyza)
|-
|-

Revision as of 17:22, 12 December 2010

DPP4 Inhibitor Pharmacokinetics
Parameter Vildagliptin
(Galvus)
Sitagliptin
(Januvia)
Saxagliptin
(Onglyza)
Tmax (hr) 1.75 1-4 2
Cmax (ng/ml) Vildagliptin
(Galvus)
Sitagliptin
(Januvia)
Saxagliptin
(Onglyza)
Bioavailability (%) 85 87 [67
Protein Binding (%) 9 38 0
T1/2 (hr) 2-3 12.4 2.5
AUC (ng/ml/hr) Vildagliptin
(Galvus)
Sitagliptin
(Januvia)
Saxagliptin
(Onglyza)
IC50 (nM) 3 18 Saxagliptin
(Onglyza)
Renal Clearance (L/h) 13.0 21.0 13.8
Dosage (mg) 100 100 5
Metabolism Vildagliptin
(Galvus)
Sitagliptin
(Januvia)
Saxagliptin
(Onglyza)

For Pharmacokinetic Data References, see: References

Proteopedia Page Contributors and Editors (what is this?)

David Canner

Personal tools