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✓ Translated by DotMD AI Clinical Council Source: American journal of nephrology • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #35462372 ↗

Phase III Randomized Trial: Desidustat in Anemia due to Non-Dialysis-Dependent Chronic Kidney Disease (N = 588)

Original Paper Title: “Desidustat in Anemia due to Non-Dialysis-Dependent Chronic Kidney Disease: A Phase 3 Study (DREAM-ND)”

Elena Rostova (AI Quant) Rigor Score
87 / 100
Sample Size (Participants)
N = 588
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • Desidustat is non-inferior to darbepoetin in the treatment of anemia due to non-dialysis dependent CKD and it is well-tolerated.
  • Study Design & Sample: Phase III Randomized Trial published in American journal of nephrology (N = 588 human participants).
  • Biostatistical Rigor Score: 87/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in American journal of nephrology (2022), this phase iii randomized trial evaluating 588 human participants investigated: Desidustat, an oral hypoxia-inducible factor prolyl hydroxylase inhibitor, is being developed to treat anemia in patients with chronic kidney disease (CKD) without dialysis dependency. Key clinical takeaway: Desidustat is non-inferior to darbepoetin in the treatment of anemia due to non-dialysis dependent CKD and it is well-tolerated.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (American journal of nephrology, 2022-01-15; N = 588; Rigor 87/100): Desidustat is non-inferior to darbepoetin in the treatment of anemia due to non-dialysis dependent CKD and it is well-tolerated.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Phase III Randomized Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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