drugset / Trial / NCT03329196

Efficacy and Safety Study to Evaluate MT-6548 in Non-dialysis Subjects With Anemia Associated With Chronic Kidney Disease in Japan

NCT03329196 ↗

Phase 3 Completed 304 enrolled Tanabe Pharma Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

For Non-dialysis subjects with anemia associated with chronic kidney disease, demonstrate non-inferiority of MT-6548 compared to darbepoetin alfa using Hb value and evaluate long-term safety of MT-6548. For subjects not currently receiving ESAs, evaluate Hb correction and maintenance effect of MT-6548 and for subjects currently receiving ESAs, evaluate Hb conversion and maintenance effect of MT-6548

Timeline

Start
2017-10-30
Primary completion
2019-01-08
Completion
2019-08-09

Outcome

Met primary endpoint

paper demonstrating noninferiority of vadadustat to darbepoetin alfa. PMID 33883252 ↗

release “The study showed non-inferiority of MT-6548 in mean hemoglobin (Hb) level at week 20 and week 24” tanabe-pharma.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Darbepoetin alfa Protein / enzyme biologic — Subcutaneous
Subject MT-6548 Unknown — Oral

Indications