The FimAsartaN proTeinuriA SusTaIned reduCtion in comparison with losartan in diabetic chronic kidney disease (FANTASTIC) trial

Tae Hyun Yoo, Soon Jun Hong, Sunggyun Kim, Seokjoon Shin, Dong Ki Kim, Jung Pyo Lee, Sang Youb Han, Sangho Lee, Jong Chul Won, Young Sun Kang, Jongha Park, Byoung Geun Han, Ki Ryang Na, Kyu Yeon Hur, Yong Jin Kim, Sungha Park

Research output: Contribution to journalArticlepeer-review

Abstract

As angiotensin II type 1 receptor blockers (ARBs) may have different antiproteinuric effects in diabetic kidney disease (DKD), we ascertained the albuminuria-reducing effect of fimasartan and losartan in patients with DKD. This was a randomized, multicenter, double-blind, 4-parallel-group, dose-titration, phase III study designed to compare the efficacy of fimasartan and losartan in reducing albuminuria in patients with DKD (NCT02620306). The primary endpoint was the rate of change in albuminuria from baseline to week 24. A total of 341 patients were randomized to different groups. The urinary albumin-to-creatinine ratio (ACR), systolic blood pressure (SBP), and diastolic blood pressure (DBP) were not different between the fimasartan and losartan groups at baseline (ACR: 1376.84 vs. 1521.07 mg/gCr, SBP: 154.69 vs. 154.47 mmHg, DBP: 83.96 vs. 83.83 mmHg). However, ACR reduction was significantly larger in the fimasartan group than in the losartan group during the entire study period (% changes in the ACR at 4, 8, 12, and 24 weeks were –23.58, –33.06, –35.00, and –38.13 in the fimasartan group vs. –8.74, –10.17, –14.91, and –19.71 in the losartan group, p < 0.01, respectively). The superior antiproteinuric effect of fimasartan compared to losartan was still significant after adjustment for SBP levels. There were no significant differences in adverse events, including the incidences of estimated glomerular filtration decline and hyperkalemia. This study demonstrates that compared to losartan, fimasartan significantly reduces albuminuria in patients with DKD, even after adjustment for SBP and DBP.

Original languageEnglish
Pages (from-to)2008-2017
Number of pages10
JournalHypertension Research
Volume45
Issue number12
DOIs
Publication statusPublished - 2022 Dec

Bibliographical note

Funding Information:
This study was supported by Boryung Co., Ltd., Seoul, Korea. SP received lecture fees from Pfizer, Boryoung, Hanmi, Daewoong, Donga, Celltrion, Servier, Daiichi Sankyo, and Daewon. SP also received a research grant from Daiichi Sankyo. YJK received consultation fees from Celltrion and lecture fees from Yuhan, Daewoong, Daiichi Sankyo, Bayer, Takeda, and GC Pharma. SJH received lecture fees and research sponsoring from Hanmi, InnoN, Samjin, and Boryung. SGK received lecture fees and research sponsorships from Yuhan, JW Pharma, AstraZeneca, GSK, Fibrogen, Akebia, Omeros, Chinook, MorphoSys, Otsuka and Boryung. JCW received lecture fees and research sponsorships from Chong Kun Dang, Daewoong, Eli Lilly, Yuhan, and Boryung.

Publisher Copyright:
© 2022, The Author(s), under exclusive licence to The Japanese Society of Hypertension.

All Science Journal Classification (ASJC) codes

  • Internal Medicine
  • Physiology
  • Cardiology and Cardiovascular Medicine

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