Design of FLAIR: a Phase 2b Study of the 5-Lipoxygenase Activating Protein Inhibitor AZD5718 in Patients With Proteinuric CKD

被引:9
|
作者
Heerspink, Hiddo J. L. [1 ]
Law, Gordon [2 ]
Psachoulia, Konstantina [3 ]
Connolly, Kathleen [4 ]
Whatling, Carl [5 ]
Ericsson, Hans [6 ]
Knochel, Jane [6 ]
Lindstedt, Eva-Lotte [7 ]
MacPhee, Iain [4 ]
机构
[1] Univ Groningen, Dept Clin Pharm & Pharmacol, Univ Med Ctr Groningen, Groningen, Netherlands
[2] AstraZeneca, Early Biometr & Stat Innovat, Data Sci & Artificial Intelligence, R&D, Gaithersburg, MD USA
[3] AstraZeneca, Early Clin Dev, Res & Early Dev, Cardiovasc Renal & Metab,BioPharmaceut R&D, Gaithersburg, MD USA
[4] AstraZeneca, Early Clin Dev, Res & Early Dev, Cardiovasc Renal & Metab,BioPharmaceut R&D, Cambridge, England
[5] AstraZeneca, Translat Sci & Expt Med, Res & Early Dev, Cardiovasc Renal & Metab,BioPharmaceut R&D, Gothenburg, Sweden
[6] AstraZeneca, BioPharmaceut R&D, Clin Pharmacol & Safety Sci, Clin Pharmacol & Quantitat Pharmacol, Gothenburg, Sweden
[7] AstraZeneca, Res & Early Clin Dev, Cardiovasc Renal & Metab, BioPharmaceut R&D, Gothenburg, Sweden
来源
KIDNEY INTERNATIONAL REPORTS | 2021年 / 6卷 / 11期
关键词
albuminuria; chronic kidney disease; diabetic kidney disease; leukotriene; 5-lipoxygenase activating protein; randomized controlled clinical trial; CHRONIC KIDNEY-DISEASE; CARDIOVASCULAR OUTCOMES; SERUM CREATININE; INFLAMMATION; MECHANISMS; MORTALITY;
D O I
10.1016/j.ekir.2021.08.018
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Patients with chronic kidney disease (CKD) remain at risk for kidney and cardiovascular events resulting from residual albuminuria, despite available treatments. Leukotrienes are proin-flammatory and vasoconstrictive lipid mediators implicated in the etiology of chronic inflammatory dis-eases. AZD5718 isa potent, selective, and reversible 5-lipoxygenase activating protein (FLAP) inhibitor that suppresses leukotriene production. Methods: FLAIR (FLAP Inhibition in Renal disease) is an ongoing phase 2b, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of AZD5718 in patients with proteinuric CKD with or without type 2 diabetes. Participants receive AZD5718 at 3 different doses or placebo once daily for 12 weeks, followed by an 8-week extension in which they also receive dapagliflozin (10 mg/d) as anticipated future standard of care. The planned sample size is 632 participants, providing 91% power to detect 30% reduction in urinary albumin-to-creatinine ratio (UACR) between the maximum dose of AZD5718 and placebo. The dose-response effect of AZD5718 on UACR after the dapagliflozin extension is the primary efficacy objective. Key secondary objectives are the dose-response effect of AZD5718 plus current standard of care on UACR and acute effects of treatment on the estimated glomerular filtration rate. Safety, tolerability, AZD5718 pharmacokinetics, and ana-lyses of biomarkers that may predict or reflect response to AZD5718 are additional objectives. Conclusion: FLAIR will provide data on the effects of 5-lipoxygenase pathway inhibition in patients with proteinuric CKD with or without type 2 diabetes, and will form the basis for future clinical trials.
引用
收藏
页码:2803 / 2810
页数:8
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