Abstract
Objective: To assess the impact of non-medical switch (NMS) from canagliflozin on antihyperglycemic agent (AHA) medication taking behavior.
Methods: This retrospective real-world database analysis included patients with type 2 diabetes with a prescription claim for canagliflozin (CANA) between August 2015 and January 2016 using administrative claims and longitudinal prescription data. Patients with NMS from canagliflozin were identified as those with discontinuation or switch of canagliflozin and enrolled in a pharmacy benefit manager that removed CANA from formulary in 2016. Patients with NMS were propensity score matched to patients without NMS. Patients had a 6 month baseline period and a 4 month follow-up period.
Results: The study sample comprised 668 patients with NMS matched to 668 patients without NMS (52.4% and 49.9% male, mean age 55.6 and 55.7, respectively). Among patients with NMS, half (52.8%) did not switch to a new AHA medication (i.e. abandoned therapy) after discontinuation of CANA, while the remaining 47.2% switched to a new AHA medication. Over the 4 month follow-up, patients with NMS used significantly fewer unique AHA products compared to patients without NMS (mean [SD] 2.13 [1.40] vs. 2.66 [1.02], p < .0001). Over the 4 month follow-up, 16.5% of patients with NMS had no use of any AHA; by definition, patients without NMS used at least 1 AHA (i.e. canagliflozin).
Conclusions: Among patients with NMS, therapy abandonment was a major unintended consequence. Further research is needed to investigate the impact of NMS on clinical outcomes as well as the impact of NMS over a longer follow-up.
Transparency
Declaration of funding
This study was sponsored by Janssen Research & Development LLC.
Declaration of financial/other relationships
B.B., J.C. and M.P. have disclosed that they are employees and shareholders of Janssen. C.B. and V.D. have disclosed that they are employees of IQVIA which received funding for this study from Janssen. L.B. has disclosed that he is employed by the Ochsner Medical Center and was a consultant to Janssen on this study and for other activities, and a promotional speaker for Janssen and Invokana. C.I.C. has disclosed that he is employed by the University of Connecticut School of Pharmacy and the Hartford Hospital Evidence-Based Practice Center and was a consultant to Janssen on this study.
A CMRO peer reviewer on this manuscript declares consultancy to Janssen Pharmaceuticals, who manufacture Invokana. Other CMRO peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Acknowledgements
None reported.
Note
Notes
*Canagliflozin (INVOKANA®)