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Abstract: FR-PO324

Utilization of Guideline-Directed Medical Therapies in Finerenone Users

Session Information

Category: Diabetic Kidney Disease

  • 702 Diabetic Kidney Disease: Clinical

Authors

  • Zheng, Zihe, Bayer US, LLC, Whippany, New Jersey, United States
  • Fatoba, Samuel T., Bayer US, LLC, Whippany, New Jersey, United States
  • Novin, Matthew, Bayer US, LLC, Whippany, New Jersey, United States
  • Guerrero, German, Bayer US, LLC, Whippany, New Jersey, United States
  • Wang, Yunxun, Bayer US, LLC, Whippany, New Jersey, United States
  • Farag, Youssef MK, Bayer US, LLC, Whippany, New Jersey, United States
  • Mckee, Connor W., Cobbs Creek Healthcare LLC, Newtown Square, Pennsylvania, United States
  • Tian, Hongping, Cobbs Creek Healthcare LLC, Newtown Square, Pennsylvania, United States
  • Singh, Rakesh, Bayer US, LLC, Whippany, New Jersey, United States
  • Du, Yuxian, Bayer US, LLC, Whippany, New Jersey, United States
  • Mares, Jon W., Bayer US, LLC, Whippany, New Jersey, United States
  • Rockett, Drew, Bayer US, LLC, Whippany, New Jersey, United States
  • Sankaralingam, Karthik, Bayer US, LLC, Whippany, New Jersey, United States
  • Huang, Wei, Cobbs Creek Healthcare LLC, Newtown Square, Pennsylvania, United States
  • Lavagnino, Marco, Bayer US, LLC, Whippany, New Jersey, United States
Background

Non-steroidal MRA finerenone reduces CV risk and slows CKD progression in patients with CKD and T2D. Clinical guidelines recommend finerenone for patients with UACR > 30mg/g despite maximum tolerated RAS inhibitor (ACEi/ARB). However, it is reported that 30-50% of patients with CKD and T2D do not receive ACEi/ARBs, and about 30% of those discontinue within 6 months, contributing to the inertia for new disease-modifying therapies. To address this inertia, we assess the key characteristics of finerenone users in real-world setting with and without concomitant ACEi/ARB.

Methods

We conducted a retrospective study of finerenone users from July 2021 to December 2023 using the IQVIA Longitudinal Access and Adjudication Data. Adult patients with ≥ 12 months of continuous activity prior to their first filled finerenone claim date (index) were included. Patient demographics, comorbidities, and comedications stratified by ACEi/ARB status were described.

Results

The largest finerenone user cohort of 107,323 patients were included, among them 49,864 (46.5%) initiated finerenone in the absence of concomitant ACEi/ARB therapy. Patient age, gender, and key comorbidities were largely comparable, except for that finerenone users without ACEi/ARB had slightly higher prevalence of HF (22%) compared to those with ACEi/ARB (16%). Comedications use were 3-10% less common in the finerenone user without ACEi/ARB group, including SGLT2is and GLP1RAs. Interestingly, 5,077 (4.7%) finerenone users initiated SGLT2i after starting finerenone.

Conclusion

Our study shows that 46.5% patients initiated finerenone without concomitant ACEi/ARB. Finerenone use in the absence of ACEi/ARBs is common in routine clinical practice, suggesting that despite guideline recommendations, therapies are used in a variety of sequences and combinations to accommodate patient profiles. Future study should examine CV, kidney, and safety outcomes of finerenone users with and without ACEi/ARB.

Funding

  • Commercial Support – Bayer US LLC