A PK/PD study comparing twice-daily to
once-daily dosing regimens of ertugliflozin in healthy subjects
Vikas Kumar Dawra1*, Yali Liang1*, Haihong Shi1, Almasa Bass2*, Anne Hickman1, Steven G. Terra3, Susan Zhou4, David Cutler4*, Vaishali Sahasrabudhe1
1 Pfizer Inc., Groton, CT, 2 Pfizer Inc., Durham, NC, 3 Pfizer Inc., Andover, MA, and 4 Merck & Co., Inc., Kenilworth, NJ, USA
DOI 10.5414/CP203343
Abstract
Objective: Ertugliflozin is approved in the US and European Union as a stand-alone product for adults with type 2 diabetes mellitus as once daily (QD) dosing. The approved fixed-dose combination (FDC) of ertugliflozin and immediate-release metformin is dosed twice daily (BID). This study assessed steady-state pharmacokinetics (PK; area under the concentration-time curve over 24 hours (AUC<sub>24</sub>)) and pharmacodynamics (PD; urinary glucose excretion over 24 hours (UGE<sub>24</sub>)) for ertugliflozin 5 and 15 mg total daily doses administered BID or QD. Materials and methods: In this open-label, two-cohort, randomized, multiple-dose, crossover study, healthy subjects received ertugliflozin 2.5 mg BID and 5 mg QD (n = 28) or ertugliflozin 7.5 mg BID and 15 mg QD (n = 22) for 6 days. Plasma and urine samples were collected for 24 hour post morning dose on day 6 in each period. Results: The geometric mean ratio (GMR) (90% CI) of ertugliflozin AUC<sub>24</sub> was 100.8% (98.8%, 102.8%) for 2.5 mg BID vs. 5 mg QD, and 99.7% (97.1%, 102.5%) for 7.5 mg BID vs. 15 mg QD. GMR (90% CI) of UGE<sub>24</sub> for BID vs. QD administration was 110.2% (103.0%, 117.9%) at a total daily dose of 5 mg, and 102.8% (97.7%, 108.1%) at 15 mg. The 90% CIs of the GMR of AUC<sub>24</sub> and UGE<sub>24</sub> for BID vs. QD dosing were within the acceptance range for equivalence (80 – 125%) and the prespecified criterion for similarity (70 – 143%), respectively. All treatments were well tolerated. Conclusion: There are no clinically meaningful differences in steady-state PK or PD between ertugliflozin BID and QD regimens at total daily doses of 5 and 15 mg, supporting BID administration of ertugliflozin as a component of the ertugliflozin/metformin (immediate-release) FDC.
*At the time of study conduct
Author Details
Authors
Departments
- 1 Pfizer Inc., Groton, CT,
- 2 Pfizer Inc., Durham, NC,
- 3 Pfizer Inc., Andover, MA, and
- 4 Merck & Co., Inc., Kenilworth, NJ, USA
Address
Vikas Kumar Dawra, MBA, PhD
Quantitative Clinical Pharmacology
Daiichi Sankyo Inc.
211 Mt Airy Road, 3A-609
Basking Ridge, NJ 07920, USA
Email:
[email protected]
Citation
Vikas Kumar Dawra, Yali Liang, Haihong Shi, Almasa Bass, Anne Hickman, Steven G. Terra, Susan Zhou, David Cutler, and Vaishali Sahasrabudhe.A PK/PD study comparing twice-daily to
once-daily dosing regimens of ertugliflozin in healthy subjects
. 2019; 57: 207-216. doi: 10.5414/CP203343.