Introduction: Renal anemia is a common complication among patients with non-dialysis chronic kidney disease (ND-CKD), and there remains an unmet need for more efficient and convenient daily oral medications to improve patient outcomes. This study aimed to evaluate the efficacy and safety of enarodustat, a hypoxia-inducible factor-prolyl hydroxylase inhibitor, in treating anemia for ND-CKD patients.

Methods: This phase 3 study was conducted at 48 centers across China, enrolling 156 ND-CKD patients. Participants were randomly randomized in a 2:1 ratio to receive either enarodustat or placebo for an initial 8-week double-blind period, followed by a 16-week open-label period during which all patients received enarodustat.

Results: The primary endpoint was the mean change in hemoglobin (Hb) levels from baseline to the average level during weeks 7-9. Secondary endpoints focused on Hb concentration or treatment pattern, while exploratory endpoints assessed iron metabolism-related parameters. The mean (±SD) change in Hb levels from baseline to weeks 7-9 was 15.99 (±9.46) g/L in the enarodustat group, compared to -0.14 (±8.08) g/L in the placebo group, resulting in a mean difference of 16.00 (±1.54) g/L (.). During weeks 7-9, 85.3% of patients in the enarodustat group achieved Hb levels ≥100 g/L with 86.0% maintaining this level during weeks 21-25. In the first 4 weeks, the Hb increased by 11.82 (±9.56) g/L in the enarodustat group. By week 9, the mean change in hepcidin level was -42.94 (±37.56) ng/mL in the enarodustat group, compared to +4.58 (±33.34) ng/mL in the placebo group. Enarodustat also improved other iron-related parameters and reduced the need for iron supplements. The safety profile of enarodustat was well tolerable with adverse events comparable to those of the placebo.

Conclusion: Enarodustat effectively corrected renal anemia with a manageable safety profile. Its once-daily oral administration offers convenience that may enhance the adherence. Enarodustat shows the potential as a promising therapy for anemic patients with ND-CKD.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11805549PMC
http://dx.doi.org/10.1159/000543193DOI Listing

Publication Analysis

Top Keywords

enarodustat group
16
weeks 7-9
12
enarodustat
11
patients non-dialysis
8
non-dialysis chronic
8
chronic kidney
8
kidney disease
8
renal anemia
8
levels baseline
8
level weeks
8

Similar Publications

Enarodustat for the Treatment of Anemia in Chinese Patients with Non-Dialysis Chronic Kidney Disease: A Phase 3 Trial.

Kidney Dis (Basel)

December 2024

Department of Nephrology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China.

Introduction: Renal anemia is a common complication among patients with non-dialysis chronic kidney disease (ND-CKD), and there remains an unmet need for more efficient and convenient daily oral medications to improve patient outcomes. This study aimed to evaluate the efficacy and safety of enarodustat, a hypoxia-inducible factor-prolyl hydroxylase inhibitor, in treating anemia for ND-CKD patients.

Methods: This phase 3 study was conducted at 48 centers across China, enrolling 156 ND-CKD patients.

View Article and Find Full Text PDF
Article Synopsis
  • - HIF-PHIs are newly developed drugs aimed at treating anemia related to chronic kidney disease (CKD) by enhancing the body's erythropoietin production and improving iron absorption.
  • - Recent studies suggest that HIF-PHIs are as effective and safe as standard treatments for CKD-related anemia, though long-term effects, especially regarding potential risks like cancer and cardiovascular events, remain uncertain.
  • - The Italian Society of Nephrology has endorsed a position paper to adapt KDIGO's recent findings about HIF-PHIs to Italy, considering their effectiveness, safety, and application in specific patient groups.
View Article and Find Full Text PDF

.

Drug Metab Dispos

February 2024

Pharmacokinetics Dynamics and Metabolism, Pfizer Inc, United States

Article Synopsis
  • OATP1B is crucial for the liver's ability to remove high molecular weight acids and zwitterions; this study investigates its role in the uptake of low molecular weight hypoxia-inducible factor prolyl hydroxylase inhibitors, known as "Dustats."
  • Five specific acid dustats were shown to be transported by OATP1B1/1B3 in lab cells, while a neutral compound (molidustat) was not transported by these transporters.
  • The use of rifampin, an OATP1B inhibitor, significantly affected the uptake and clearance of these acids in both human liver cells and in monkey studies, highlighting the importance of OATP1B in their pharmacokinetics.
View Article and Find Full Text PDF

Enarodustat (JTZ-951) is a hypoxia-inducible factor prolyl hydroxylase inhibitor that has been approved and marketed in Japan for patients with anemia with chronic kidney disease (CKD). The pharmacometric approach was applied to assess the relationship between plasma concentrations of enarodustat and hemoglobin (Hb) levels, and to provide information regarding the optimal use of enarodustat in clinical practice by simulations based on the pharmacokinetic and pharmacodynamic (PK/PD) model that was developed. The PK/PD data of enarodusat obtained from phase 2 and phase 3 studies in Japanese patients with CKD were well described by the models: a 1-compartment model with first-order absorption and elimination for PK, and a semimechanistic model based on transit compartment model for PD.

View Article and Find Full Text PDF
Article Synopsis
  • Hypoxia inducible factors (HIFs) respond to low oxygen levels by accumulating when their regulators, the prolyl hydroxylase domain enzymes (PHDs), are suppressed, leading to increased expression of genes related to survival and metabolism.
  • A new class of drugs called HIF-PHDs inhibitors (HIF-PHIs) has been developed to stimulate HIFs, with some like roxadustat and daprodustat already approved for treating anemia in chronic kidney disease.
  • Research is expanding the use of these HIF-PHIs beyond just anemia, exploring their potential in various other diseases and conditions.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!