Journal

Kidney International Reports

Publication Date

12-5-2020

Volume

6

Issue

3

First Page

624

Last Page

635

Document Type

Open Access Publication

DOI

10.1016/j.ekir.2020.11.034

1-s2.0-S2468024920317915-mmc1.pdf (341 kB)
Figure S1. Subgroup analysis of the primary US efficacy endpoint (ITT). Figure S2. Subgroup analysis of the primary EU efficacy endpoint (FAS). Table S1. Inclusion and exclusion criteria. Table S2. Roxadustat dose adjustment algorithm. Table S3. Fixed sequence for testing secondary efficacy endpoints. Table S4. Change from baseline to weeks 12 to 28 in LDL cholesterol by treatment and statin use (FAS). Table S5. Mean change from baseline for hepcidin and iron-related parameters at week 44 (FAS). Table S6. Summary of TEAEs∗ occurring in ≥5% of patients in either treatment group (W52) (SAF). Table S7. Summary of TESAEs∗ occurring in ≥1% of patients in either treatment group (W52) (SAF).

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